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Current Oncology is published by MDPI from Volume 28 Issue 1 (2021). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Multimed Inc..

Curr. Oncol., Volume 23, Issue 5 (October 2016) – 25 articles

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68 KiB  
Correction
Corrigendum: Did the Addition of Concomitant Chemotherapy to Radiotherapy Improve Outcomes in Hypopharyngeal Cancer? A Population-Based Study
by S.F. Hall and R. Griffiths
Curr. Oncol. 2016, 23(5), 526; https://doi.org/10.3747/co.23.3435 - 01 Oct 2016
Viewed by 405
Abstract
The ledfs was 37.8% before 2000 (all patients treated with rt).[...] Full article
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Article
Sunrise in Gagliato
by H.S. Wald
Curr. Oncol. 2016, 23(5), 523-525; https://doi.org/10.3747/co.23.3260 - 01 Oct 2016
Viewed by 373
Abstract
Sunrise in Gagliato, [...] Full article
102 KiB  
Article
Book review: Balanced Ethics Review: A Guide for Institutional Review Board Members
by T. Christie
Curr. Oncol. 2016, 23(5), 521-522; https://doi.org/10.3747/co.23.3354 - 01 Oct 2016
Viewed by 371
Abstract
Balanced Ethics Review is intended to be a guide for members of Institutional Review Boards[...] Full article
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Review
Adult-Onset Kaposiform Hemangioendothelioma of the Tongue: Case Report and Review of the Literature
by P. Vashi, E. Abboud, C. Bier-Laning and D. Gupta
Curr. Oncol. 2016, 23(5), 517-520; https://doi.org/10.3747/co.23.3239 - 01 Oct 2016
Cited by 7 | Viewed by 381
Abstract
We present here a very rare clinical case of a 38-year-old man with Kaposiform hemangioendothelioma (KHE) of the tongue who presented to our institution with a growth under the left side of the tongue with no pain or discomfort. There were [...] Read more.
We present here a very rare clinical case of a 38-year-old man with Kaposiform hemangioendothelioma (KHE) of the tongue who presented to our institution with a growth under the left side of the tongue with no pain or discomfort. There were no enlarged lymph nodes and no significant neurologic findings. Diagnostic histopathology confirmed the lesion to be KHE. The tumour was removed surgically, and the surgical specimen confirmed the diagnosis. Follow-up at 3 months shows no clinical evidence of recurrence. Full article
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Article
Painless Neutropenic Enterocolitis in a Patient Undergoing Chemotherapy
by E.J. Chow and K.D. Bishop
Curr. Oncol. 2016, 23(5), 514-516; https://doi.org/10.3747/co.23.3119 - 01 Oct 2016
Cited by 4 | Viewed by 440
Abstract
Case Description: A 60-year-old man developed painless neutropenic enterocolitis after induction chemotherapy for newly diagnosed acute myelogenous leukemia. The patient had recurrent fever while neutropenic, without experiencing abdominal pain or tenderness on physical examination. His diagnosis was delayed by the fact that he [...] Read more.
Case Description: A 60-year-old man developed painless neutropenic enterocolitis after induction chemotherapy for newly diagnosed acute myelogenous leukemia. The patient had recurrent fever while neutropenic, without experiencing abdominal pain or tenderness on physical examination. His diagnosis was delayed by the fact that he had no localizing symptoms. Discussion: Neutropenic enterocolitis is a common complication, generally occurring in patients who are severely neutropenic; the condition presents with fever and abdominal pain. No cases of painless neutropenic enterocolitis have yet been reported. Review of the literature shows that patients can develop this condition in the absence of fever and, sometimes, neutropenia. Furthermore, few comprehensive studies or reviews have investigated the utility of computed tomography imaging in identifying a source for abdominal pain in neutropenic patients with fever. Many potential causes of febrile neutropenia should be considered in chemotherapy patients. Full article
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Article
Follow-Up Care for Survivors of Lymphoma Who Have Received Curative-Intent Treatment
by J. Sussman, N.P. Varela, M. Cheung, L. Hicks, D. Kraftcheck, J. Mandel, G. Fraser, L. Jimenez-Juan, A. Boudreau, S. Sajkowski and R. McQuillan
Curr. Oncol. 2016, 23(5), 499-513; https://doi.org/10.3747/co.23.3265 - 01 Oct 2016
Cited by 6 | Viewed by 432
Abstract
Objective: This evidence summary set out to assess the available evidence about the follow-up of asymptomatic survivors of lymphoma who have received curative-intent treatment. Methods: The MEDLINE and EMBASE databases and the Cochrane Database of Systematic Reviews were searched for evidence published between [...] Read more.
Objective: This evidence summary set out to assess the available evidence about the follow-up of asymptomatic survivors of lymphoma who have received curative-intent treatment. Methods: The MEDLINE and EMBASE databases and the Cochrane Database of Systematic Reviews were searched for evidence published between 2000 and August 2015 relating to lymphoma survivorship follow-up. The evidence summary was developed by a Working Group at the request of the Cancer Care Ontario Survivorship and Cancer Imaging programs because of the absence of evidence-based practice documents in Ontario for the follow-up and surveillance of asymptomatic patients with lymphoma in complete remission. Results: Eleven retrospective studies met the inclusion criteria. The proportion of relapses initially detected by clinical manifestations ranged from 13% to 78%; for relapses initially detected by imaging, the proportion ranged from 8% to 46%. Median time for relapse detection ranged from 8.6 to 19 months for patients initially suspected because of imaging and from 8.6 to 33 months for those initially suspected because of clinical manifestations. Only one study reported significantly earlier relapse detection for patients initially suspected because of clinical manifestations (mean: 4.5 months vs. 6.0 months, p = 0.042). No benefit in terms of overall survival was observed for patients depending on whether their relapse was initially detected because of clinical manifestations or surveillance imaging. Findings in the present study support the importance of improving awareness on the part of survivors and clinicians about the symptoms that might be associated with recurrence. The evidence does not support routine imaging for improving outcomes in this patient population. Full article
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Article
Survivorship Care Plans for People with Colorectal Cancer: Do They Reflect the Research Evidence?
by V. D’Souza, H. Daudt and A. Kazanjian
Curr. Oncol. 2016, 23(5), 488-498; https://doi.org/10.3747/co.23.3114 - 01 Oct 2016
Cited by 7 | Viewed by 500
Abstract
Aim: In the present study, we synthesized the published literature about the psychosocial aspects of colorectal cancer (crc) survivorship to support an update of the evidentiary base of the survivorship care plans (scps) created in our jurisdiction. Methods: The [...] Read more.
Aim: In the present study, we synthesized the published literature about the psychosocial aspects of colorectal cancer (crc) survivorship to support an update of the evidentiary base of the survivorship care plans (scps) created in our jurisdiction. Methods: The psychosocial topics identified in the crc scps created by two different initiatives in our province were used as search criteria: quality of life (qol), sexual function, fatigue, and lifestyle behaviors. An umbrella review was conducted to retrieve the best possible evidence. Only reviews that investigated the intended outcomes in crc survivors and those with moderate-to-high methodologic quality scores were included. Results: Of 462 retrieved reports, eight reviews met the inclusion criteria for the synthesis. Of those eight, six investigated the challenges of crc survivors and two investigated the effect of physical activity on survivor well-being. Our results indicate that emotional and physical challenges are common in crc survivors and that physical activity is associated with clinically important benefits for the fatigue and physical functioning of crc survivors. Conclusions: Our study findings update the evidence and indicate that existing scps in our province concerning the physical and emotional challenges of crc survivors reflect the evidence at the time of their issue. However, the literature concerning cancer risks specific to crc survivors is lacking. Although systematic reviews are considered to be the “gold standard” in knowledge synthesis, our findings suggest that much remains to be done in the area of synthesis research to better guide practice in cancer survivorship. Full article
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Article
Bioelectrical Impedance Phase Angle as a Prognostic Indicator of Survival in Head-and-Neck Cancer
by M.S. Władysiuk, R. Mlak, K. Morshed, W. Surtel, A. Brzozowska and T. Małecka-Massalska
Curr. Oncol. 2016, 23(5), 481-487; https://doi.org/10.3747/co.23.3181 - 01 Oct 2016
Cited by 34 | Viewed by 633
Abstract
Background: Phase angle could be an alternative to subjective global assessment for the assessment of nutrition status in patients with head-and-neck cancer. Methods: We prospectively evaluated a cohort of 75 stage IIIB and IV head-and-neck patients treated at the Otolaryngology Department, Head and [...] Read more.
Background: Phase angle could be an alternative to subjective global assessment for the assessment of nutrition status in patients with head-and-neck cancer. Methods: We prospectively evaluated a cohort of 75 stage IIIB and IV head-and-neck patients treated at the Otolaryngology Department, Head and Neck Surgery, Medical University of Lublin, Poland. Bioelectrical impedance analysis was performed in all patients using an analyzer that operated at 50 kHz. The phase angle was calculated as reactance divided by resistance (Xc/R) and expressed in degrees. The Kaplan–Meier method was used to calculate survival. Results: Median overall survival in the cohort was 32.0 months. At the time of analysis, 47 deaths had been recorded in the cohort (62.7%). The risk of shortened overall survival was significantly higher in patients whose phase angle was less than 4.733 degrees than in the remaining patients (19.6 months vs. 45 months, p = 0.0489; chi-square: 3.88; hazard ratio: 1.8856; 95% confidence interval: 1.0031 to 3.5446). Conclusions: Phase angle might be prognostic of survival in patients with advanced head-and-neck cancer. Further investigation in a larger population is required to confirm our results. Full article
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Article
Combined Sorafenib and Yttrium-90 Radioembolization for the Treatment of Advanced Hepatocellular Carcinoma
by A. Salman, E. Simoneau, M. Hassanain, P. Chaudhury, L.M. Boucher, D. Valenti, T. Cabrera, C. Nudo and P. Metrakos
Curr. Oncol. 2016, 23(5), 472-480; https://doi.org/10.3747/co.23.2827 - 01 Oct 2016
Cited by 12 | Viewed by 556
Abstract
Background and Aims: In this pilot study, we assessed the safety and tolerability of combining sorafenib with 90Y radioembolization for the treatment of unresectable hepatocellular carcinoma (HCC). Methods: The study, conducted prospectively during 2009–2012, included eligible patients with [...] Read more.
Background and Aims: In this pilot study, we assessed the safety and tolerability of combining sorafenib with 90Y radioembolization for the treatment of unresectable hepatocellular carcinoma (HCC). Methods: The study, conducted prospectively during 2009–2012, included eligible patients with unresectable HCC and a life expectancy of at least 12 weeks. Each patient received sorafenib (400 mg twice daily) for 6–8 weeks before 90Y treatment. Safety and tolerability were assessed. Results: Of the 40 patients enrolled, 29 completed treatment (combined therapy). In the initial cohort, the most common cause of HCC was hepatitis C (32.5%), and most patients were staged Child A (82.5%). The 29 patients who completed the study had similar baseline characteristics. Grades 1 and 2 toxicities accounted for 77.8% of all adverse events reported. The most common toxicities reported were fatigue (19.0%), alteration in liver function (7.9%), and diarrhea (6.3%). There were 12 grade 3 and 2 grade 4 toxicity events reported. One patient died of liver failure within 30 days after treatment. During the study, the sorafenib dose was reduced in 6 patients (20.7%), and sorafenib had to be interrupted in 4 patients (13.8%) and discontinued in 4 patients (13.8%). The disease control rate was 72.4% per the modified Response Evaluation Criteria in Solid Tumors, and tumour necrosis was observed in 82.8% of patients. Overall survival in patients undergoing combined therapy was 12.4 months. Conclusions: Preliminary results demonstrate the safety and tolerability of combining 90Y radioembolization and sorafenib for advanced HCC. A larger prospective study is needed to determine the extent of the survival benefit. Full article
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Article
Progression Pattern and Adverse Events with Bevacizumab in Glioblastoma
by A. Mamo, A. Baig, M. Azam, Y.S. Rho, S. Sahebjam, T. Muanza, S. Owen, K. Petrecca, M.C. Guiot, J. Al-Shami, R. Sharma and P. Kavan
Curr. Oncol. 2016, 23(5), 468-471; https://doi.org/10.3747/co.23.3108 - 01 Oct 2016
Cited by 8 | Viewed by 745
Abstract
Background: The use of bevacizumab in the management of glioblastoma multiforme (gbm) remains controversial. In Canada, bevacizumab is approved for the treatment of recurrent gbm. We describe a pattern of progression across treatment lines in gbm. Methods: During 2008–2014, 64 [...] Read more.
Background: The use of bevacizumab in the management of glioblastoma multiforme (gbm) remains controversial. In Canada, bevacizumab is approved for the treatment of recurrent gbm. We describe a pattern of progression across treatment lines in gbm. Methods: During 2008–2014, 64 patients diagnosed with gbm were treated with bevacizumab at McGill University hospitals. Of those patients, 30 (46.9%) received bevacizumab in the first line (B1L), and 34 (53.1%) received it in the second line and beyond (B2L+). The average length of treatment with bevacizumab was 24.4 weeks (range: 0–232.7 weeks). The patterns of progression were categorized as local, distant, diffuse, multifocal, or multi-pattern. Results: Local progression was seen in 46.7% of B1L patients and 26.5% of B2L+ patients, distant in 3.3% and 2.9%, diffuse in 20% and 47%, multifocal in 10% and 8.8%, and multi-pattern in 3.3% and 11.8%. No differences between the groups were observed for the distant (p = 0.3) or diffuse (p = 0.4) patterns. Grades 3 and 4 adverse events in the B1L and B2L+ groups were fatigue (33.3% vs. 17.6% respectively), hypertension (26.7% vs. 5.9%), thrombocytopenia (26.7% vs. 11.8%), neutropenia (26.7% vs. 11.8%), anemia (23.3% vs. 11.8%), leucopenia (20% vs. 8.8%), deep vein thrombosis (23.3% vs. 5.9%), seizure (16.7% vs. 8.8%), brain hemorrhage (6.7% vs. <1%), and delayed wound healing (6.7% vs. 2.9%). More total grades 3 and 4 adverse events occurred in the B1L group (p = 0.000519). Conclusions: In our cohort, patterns of progression were not different in B1L and B2L+ patients. Moreover, both groups experienced similar adverse events, although more grades 3 and 4 events occurred in the B1L group, implying that severe adverse events in B1L patients could negatively affect survival outcomes. Full article
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Article
The Cost-Effectiveness of Bevacizumab for the Treatment of Advanced Ovarian Cancer in Canada
by M. Duong, E. Wright, L. Yin, I. Martin-Nunez, P. Ghatage and M. Fung-Kee-Fung
Curr. Oncol. 2016, 23(5), 461-467; https://doi.org/10.3747/co.23.3139 - 01 Oct 2016
Cited by 8 | Viewed by 1131
Abstract
Background: The overall survival (OS) analysis of the icon7 trial demonstrated that frontline ovarian cancer patients with a high risk of progression (stage III suboptimally debulked, and stage III or IV with unresectable disease) benefited from the addition of bevacizumab to [...] Read more.
Background: The overall survival (OS) analysis of the icon7 trial demonstrated that frontline ovarian cancer patients with a high risk of progression (stage III suboptimally debulked, and stage III or IV with unresectable disease) benefited from the addition of bevacizumab to standard chemotherapy compared with standard chemotherapy alone. The objective of the present study was to investigate the cost-effectiveness, from a Canadian publicly funded perspective, of adding bevacizumab to frontline treatment of ovarian cancer at high risk of progression. Methods: An area-under-the-curve, Markov-structured model was used to estimate the cost-effectiveness of the treatments. Long-term progression-free survival (PFS) and os were extracted from the icon7 trial (subgroup at high risk of relapse) and extrapolated by parametric time-to-event functions over a time horizon of 10 years. Canadian PFS health state utility values were obtained from the EQ-5D (EuroQoL Group, Rotterdam, Netherlands) questionnaires in the icon7 high-risk patient population. Canadian post-progression utility values were consistent with those for other gynecologic cancers. Cost inputs were informed by public sources. An annual 5% efficacy and cost discount rate was applied. A probabilistic sensitivity analysis and one-way sensitivity analyses were conducted. Results: Ovarian cancer patients at high risk of progression receiving bevacizumab plus standard chemotherapy experienced a mean incremental quality-adjusted life year (QALY) gain of 0.374 years. At an additional cost of $35,901.54, the incremental cost-effectiveness ratio (ICER) for the addition of bevacizumab to standard chemotherapy, relative to standard chemotherapy alone, was $95,942 per QALY. Conclusions: No formal health technology assessment willingness-to-pay threshold exists in Canada. However, at a threshold of $100,000 per QALY, bevacizumab in addition to chemotherapy is a cost-effective alternative for ovarian cancer patients who are at high risk of progression (stage III suboptimally debulked, and stage III or IV with unresectable disease). Using the $100,000 per qaly threshold in a probabilistic sensitivity analysis, it was determined that, compared with standard chemotherapy, the addition of bevacizumab to chemotherapy is cost-effective in 56% of tested scenarios. Full article
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Article
Cross-Comparison of Cancer Drug Approvals at Three International Regulatory Agencies
by N. Samuel and S. Verma
Curr. Oncol. 2016, 23(5), 454-460; https://doi.org/10.3747/co.23.2803 - 01 Oct 2016
Cited by 17 | Viewed by 727
Abstract
Background: The primary objective of the present study was to examine the drug approval process and the time to approval (TTA) for cancer drugs by 3 major international regulatory bodies—Health Canada, the U.S. Food and Drug Administration (FDA), [...] Read more.
Background: The primary objective of the present study was to examine the drug approval process and the time to approval (TTA) for cancer drugs by 3 major international regulatory bodies—Health Canada, the U.S. Food and Drug Administration (FDA), and the European Medicines Agency (EMA)—and to explore differences in the drug approval processes that might contribute to any disparities. Methods: The publicly available Health Canada Drug Product Database was surveyed for all marketed antineoplastic agents approved between 1 January 2005 and 1 June 2013. For the resulting set of cancer drugs, public records of sponsor submission and approval dates by Health Canada, the FDA, and the EMA were obtained. Results: Overall, the TTA for the 37 antineoplastic agents that met the study criteria was significantly less for the FDA than for the EMA (X̄ = 6.7 months, p < 0.001) or for Health Canada (X̄ = 6.4 months, p < 0.001). The TTA was not significantly different for Health Canada and the EMA (X̄ = 0.65 months, p = 0.89). An analysis of the review processes demonstrated that the primary reason for the identified discrepancies in TTA was the disparate use of accelerated approval mechanisms. Summary: In the present study, we systematically compared cancer drug approvals at 3 international regulatory bodies. The differences in TTA reflect several important considerations in the regulatory framework of cancer drug approvals. Those findings warrant an enhanced dialogue between clinicians and government agencies to understand opportunities and challenges in the current approval processes and to work toward balancing drug safety with timely access. Full article
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Article
Long-Term Health Care Costs for Prostate Cancer Patients on Androgen Deprivation Therapy
by M.D. Krahn, K.E. Bremner, J. Luo, G. Tomlinson and S.M.H. Alibhai
Curr. Oncol. 2016, 23(5), 443-453; https://doi.org/10.3747/co.23.2953 - 01 Oct 2016
Cited by 8 | Viewed by 530
Abstract
Background: Comparing relative costs for androgen deprivation therapy (ADT) protocols in prostate cancer (PCa) requires an examination of all health care resources, not only those specific to PCa. The objective of the present study was to use administrative [...] Read more.
Background: Comparing relative costs for androgen deprivation therapy (ADT) protocols in prostate cancer (PCa) requires an examination of all health care resources, not only those specific to PCa. The objective of the present study was to use administrative data to estimate total health care costs in a population-based cohort of PCa patients. Methods: Patients in Ontario with PCa who started 90 days or more of ADT at age 66 years or older during 1995–2005 were selected from cancer registry and health care administrative databases. We classified patients (n = 21,818) by regimen (medical castration, orchiectomy, anti-androgen monotherapy, medical castration with anti-androgen, orchiectomy with anti-androgen) and indication (neoadjuvant, adjuvant, metastatic disease, biochemical recurrence, primary nonmetastatic). Using nonparametric regression methods, with inverse probability weighting to adjust for censoring, and bootstrapping, we computed mean 1-year, 5-year, and 10-year longitudinal total direct medical costs (2009 Canadian dollars). Results: Mean first-year costs were highest for metastatic disease, ranging from $24,400 for orchiectomy to $32,120 for anti-androgen monotherapy. Mean first-year costs for all other indications were less than $20,000. Mean 5-year and 10-year costs were lowest for neoadjuvant treatment: approximately $43,000 and $81,000 respectively, with differences of less than $4,000 between regimens. Annual costs were highest in the first year of ADT. Orchiectomy was the least costly regimen for most time periods, but was limited to primary and metastatic indications. Outpatient drugs, including pharmacologic ADT, accounted for 17%–65% of total first-year costs. Conclusions: Compared with combined therapies, the ADT monotherapies, particularly orchiectomy when clinically feasible, are more economical. Our methods exemplified the use of algorithms to elucidate clinical information from administrative data. Our approach can be adapted for other cancers to expand the range of studies using Canadian administrative data. Full article
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Article
Serum Carcinoembryonic Antigen as a Tumour Marker in Patients with Endometrial Cancer
by Y. Hashiguchi, M. Kasai, T. Fukuda, T. Ichimura, T. Yasui and T. Sumi
Curr. Oncol. 2016, 23(5), 439-442; https://doi.org/10.3747/co.23.3153 - 01 Oct 2016
Cited by 13 | Viewed by 554
Abstract
Background: No potential tumour markers have been validated for prognosis in endometrial cancer. However, carcinoembryonic antigen (CEA) is one of the most widely used tumour markers in various types of cancer. Although CEA expression in endometrial cancer has been investigated, its [...] Read more.
Background: No potential tumour markers have been validated for prognosis in endometrial cancer. However, carcinoembryonic antigen (CEA) is one of the most widely used tumour markers in various types of cancer. Although CEA expression in endometrial cancer has been investigated, its prognostic value remains controversial, and no studies have investigated serum CEA levels in large case series. In the present study, we investigated diagnostic and prognostic applications of serum CEA for endometrial cancer. Methods: This prospective study was approved by our Institutional Review Board. Between January 2006 and December 2012, serum CEA was measured prospectively in 215 patients with endometrial cancer and was subsequently measured during treatment and at scheduled follow-up examinations in patients with elevated baseline serum CEA. Results: During the study period, 215 patients (142 stage I, 19 stage II, 32 stage III, 22 stage IV) were treated for endometrial cancer. By the time of last follow-up, 52 had relapsed (24.2%), and the median follow-up duration was 45 months (range: 1–95 months). Elevated serum CEA was identified in 25 patients (11.6%) and was associated with histologic type (p = 0.04), histologic grade (p = 0.03), and myometrial invasion depth (p = 0.01). Elevated serum CEA was not related to clinical stage, lymph node metastasis, distant metastasis, age, menopausal status, or body mass index. Relapse of disease was related to elevated serum CEA (p = 0.006). Conclusions: Serum CEA is a potential prognostic indicator for endometrial cancer. Full article
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Article
When Impatience Is a Virtue
by N. Mills
Curr. Oncol. 2016, 23(5), 436-438; https://doi.org/10.3747/co.23.3337 - 01 Oct 2016
Viewed by 355
Abstract
There can be few paradoxes quite like the life and death of the former mayor of Toronto, Rob Ford[...] Full article
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Article
Clinical Surveillance Compared with Clinical and Magnetic Resonance Imaging Surveillance for Brain Metastasis: A Feasibility Survey
by K.C.Y. Yiu and J.N. Greenspoon
Curr. Oncol. 2016, 23(5), 356-360; https://doi.org/10.3747/co.23.3155 - 01 Oct 2016
Cited by 2 | Viewed by 437
Abstract
Introduction: After stereotactic radiosurgery (SRS) for brain metastases, patients are routinely monitored with magnetic resonance imaging (MRI). The high rate of new brain metastases after SRS treatment alone might not be as concerning with modern MRI and target localization [...] Read more.
Introduction: After stereotactic radiosurgery (SRS) for brain metastases, patients are routinely monitored with magnetic resonance imaging (MRI). The high rate of new brain metastases after SRS treatment alone might not be as concerning with modern MRI and target localization treatment. Intensive surveillance might induce anxiety, lowering the patient’s quality of life (QOL). The present work is the feasibility component of a prospective study evaluating the role of surveillance MRI on QOL in patients with limited (1–3) brain metastases. Methods: Patients with limited brain metastases treated with SRS alone, an Eastern Cooperative Oncology Group performance status of 2 or less, and documented stability in treated lesions, with no new lesions seen on MRI at weeks 6–10 after SRS, were eligible. All were asked about their interest in participating in the control (MRI and clinical surveillance) or the experimental arm (symptom-directed MRI and clinical surveillance). If 33% or more agreed to participate in the experimental arm, it would be considered feasible to conduct the prospective study. Results: From November 2014 to July 2015, 45% of patients (10 of 22) agreed to participate in the experimental arm. Subgroup analyses found that the decision to participate has no statistically significant association with time of presentation (p = 0.696), display of symptoms (p = 0.840), age (p = 0.135), or number of lesions (p = 0.171). Conclusions: Results show that it is feasible to conduct the prospective cohort study. Because of the small sample size, we are limited in the conclusions able to be drawn in the subgroup analyses. However, the future study would allow for a better understanding of the attitudes of patients toward mri and its effect on qol. Full article
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Article
Use of Low-Value Radiotherapy Practices in Canada: An Analysis of Provincial Cancer Registry Data
by K. Tran, R. Rahal, M. Brundage, S. Fung, C. Louzado, M. Milosevic, J. Xu, H. Bryant and Technical Working Group
Curr. Oncol. 2016, 23(5), 351-355; https://doi.org/10.3747/co.23.3359 - 01 Oct 2016
Cited by 14 | Viewed by 551
Abstract
Background: As part of Choosing Wisely Canada (a national campaign to encourage patient–provider conversations about unnecessary medical tests, treatments, and procedures), a list of ten oncology practices that could be low-value in some instances was developed. Of those practices, two were specific to [...] Read more.
Background: As part of Choosing Wisely Canada (a national campaign to encourage patient–provider conversations about unnecessary medical tests, treatments, and procedures), a list of ten oncology practices that could be low-value in some instances was developed. Of those practices, two were specific to radiation therapy (rt): conventional fractionation as part of breast-conserving therapy (bct) for women with early-stage breast cancer, and multifraction radiation for palliation of uncomplicated painful bone metastases. Here, we report baseline findings for the current utilization rates of those two rt practices in Canada. Results: The use of conventional fractionation as part of bct varied substantially from province to province. Of women 50 years of age and older, between 8.8% (Alberta) and 36.5% (Saskatchewan) received radiation in 25 fractions (excluding boost irradiation) as part of bct. The use of hypofractionated rt (that is, 16 fractions excluding boost irradiation)—a preferred approach for many patients—was more common in all 6 reporting provinces, ranging from 43.2% in Saskatchewan to 94.7% in Prince Edward Island. The use of multifraction rt for palliation of bone metastases also varied from province to province, ranging from 40.3% in British Columbia to 69.0% in Saskatchewan. The most common number of fractions delivered to bone metastases was 1, at 50.2%; the second most common numbers were 2–5 fractions, at 41.7%. Conclusions: Understanding variation in the use of potentially low-value rt practices can help to inform future strategies to promote higher-value care, which balances high-quality care with the efficient use of limited system resources. Further work is needed to understand the factors contributing to the interprovincial variation observed and to develop benchmarks for the appropriate rate of use of these rt practices. Full article
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Guidelines
Follow-Up of Patients Who Are Clinically Disease-Free after Primary Treatment for Fallopian Tube, Primary Peritoneal, or Epithelial Ovarian Cancer: A Program in Evidence-Based Care Guideline Adaptation
by T. Le, E.B. Kennedy, J. Dodge and L. Elit
Curr. Oncol. 2016, 23(5), 343-350; https://doi.org/10.3747/co.23.3042 - 01 Oct 2016
Cited by 7 | Viewed by 536
Abstract
Background: A need for follow-up recommendations for survivors of fallopian tube, primary peritoneal, or epithelial ovarian cancer after completion of primary treatment was identified by Cancer Care Ontario’s Program in Evidence-Based Care. Methods: We searched for existing guidelines, conducted a systematic review (medline, [...] Read more.
Background: A need for follow-up recommendations for survivors of fallopian tube, primary peritoneal, or epithelial ovarian cancer after completion of primary treatment was identified by Cancer Care Ontario’s Program in Evidence-Based Care. Methods: We searched for existing guidelines, conducted a systematic review (medline, embase, and cdsr, January 2010 to March 2015), created draft recommendations, and completed a comprehensive review process. Outcomes included overall survival, quality of life, and patient preferences. Results: The Cancer Australia guidance document Follow Up of Women with Epithelial Ovarian Cancer was adapted for the Ontario context. A key randomized controlled trial found that the overall survival rate did not differ between asymptomatic women who received early treatment based on elevated serum cancer antigen 125 (CA125) alone and women who waited for the appearance of clinical symptoms before initiating treatment (hazard ratio: 0.98; 95% confidence interval: 0.80 to 1.20; p = 0.85); in addition, patients in the delayed treatment group reported good global health scores for longer. No randomized studies were found for other types of follow-up. We recommend that survivors be made aware of the potential harms and benefits of surveillance, including a discussion of the limitations of CA125 testing. Women could be offered the option of no formal follow-up or a follow-up schedule that is agreed upon by the woman and her health care provider. Education about the most common symptoms of recurrence should be provided. Alternative models of care such as nurse-led or telephone-based follow-up (or both) could be emerging options. Conclusions: The recommendations provided in this guidance document have a limited evidence base. Recommendations should be updated as further information becomes available. Full article
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Article
Predictors of Adjuvant Treatment for Pancreatic Adenocarcinoma at the Population Level
by D.J. Kagedan, M.E. Dixon, R.S. Raju, Q. Li, M. Elmi, E. Shin, N. Liu, A. El-Sedfy, L. Paszat, A. Kiss, C.C. Earle, N. Mittmann and N.G. Coburn
Curr. Oncol. 2016, 23(5), 334-342; https://doi.org/10.3747/co.23.3205 - 01 Oct 2016
Cited by 13 | Viewed by 507
Abstract
Background: In the present study, we aimed to describe, at the population level, patterns of adjuvant treatment use after curative-intent resection for pancreatic adenocarcinoma (PCC) and to identify independent predictors of adjuvant treatment use. Methods: In this observational cohort study, patients [...] Read more.
Background: In the present study, we aimed to describe, at the population level, patterns of adjuvant treatment use after curative-intent resection for pancreatic adenocarcinoma (PCC) and to identify independent predictors of adjuvant treatment use. Methods: In this observational cohort study, patients undergoing PCC resection in the province of Ontario (population 13 million) during 2005–2010 were identified using the provincial cancer registry and were linked to administrative databases that include all treatments received and outcomes experienced in the province. Patients were defined as having received chemotherapy (CTX), chemoradiation (CRT), or observation (OBS). Clinicopathologic factors associated with the use of CTX, CRT, or OBS were identified by chi-square test. Logistic regression analyses were used to identify independent predictors of adjuvant treatment versus OBS, and CTX versus CRT. Results: Of the 397 patients included, 75.3% received adjuvant treatment (27.2% CRT, 48.1% CTX) and 24.7% received obs. Within a single-payer health care system with universal coverage of costs for CTX and CRT, substantial variation by geographic region was observed. Although the likelihood of receiving adjuvant treatment increased from 2005 to 2010 (p = 0.002), multivariate analysis revealed widespread variation between the treating hospitals (p = 0.001), and even between high-volume hepatopancreatobiliary hospitals (p = 0.0006). Younger age, positive lymph nodes, and positive surgical resection margins predicted an increased likelihood of receiving adjuvant treatment. Among patients receiving adjuvant treatment, positive margins and a low comorbidity burden were associated with CRT compared with CTX. Conclusions: Interinstitutional medical practice variation contributes significantly to differential patterns in the rate of adjuvant treatment for PCC. Whether such variation is warranted or unwarranted requires further investigation. Full article
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Article
Patterns of Practice with Third-Line Anti-EGFR Antibody for Metastatic Colorectal Cancer
by M.Y. Ho, D.J. Renouf, W.Y. Cheung, H.J. Lim, C.H. Speers, C. Zhou and H.F. Kennecke
Curr. Oncol. 2016, 23(5), 329-333; https://doi.org/10.3747/co.23.3030 - 01 Oct 2016
Cited by 5 | Viewed by 528
Abstract
Background: Therapy with anti-epidermal growth factor receptor (EGFR) monoclonal antibody improves outcomes for patients with metastatic colorectal cancer (MCRC) in the first-, second-, and third-line trial settings. In British Columbia, the use of EGFR inhibitors (EGFRIS) is confined to third-line therapy, which might [...] Read more.
Background: Therapy with anti-epidermal growth factor receptor (EGFR) monoclonal antibody improves outcomes for patients with metastatic colorectal cancer (MCRC) in the first-, second-, and third-line trial settings. In British Columbia, the use of EGFR inhibitors (EGFRIS) is confined to third-line therapy, which might lower the proportion of patients who receive this therapy. The objective of the present study was to describe EGFRI treatment patterns when those agents are limited to the third-line setting. The results will inform decisions about optimal use of EGFRI agents, including earlier in the course of therapy for metastatic disease. Methods: All patients with newly diagnosed mcrc who were referred to BC Cancer Agency clinics in 2009 were included in the study. Prognostic and treatment information was prospectively collected; KRAS test results were determined by chart review. Results: The study included 443 patients with a median age of 66 years. For the 321 patients who received systemic therapy, median survival was 22.3 months. Of the 117 patients who were treated with 5-fluorouracil, oxaliplatin, and irinotecan, and who were potentially eligible for egfri therapy, 90% (105 patients) were tested for KRAS status. Of the 60 patients with KRAS wild-type tumours, 82% (49 patients) received egfri therapy. Conclusions: When EGFRI therapy is limited to the third-line setting, only a small proportion of patients receive such therapy, with death and poor performance status preventing its use in the rest. Availability of EGFRI in earlier lines of therapy could increase the proportion of patients treated with all active systemic agents. Full article
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The Prioritization Preferences of Pan-Canadian Oncology Drug Review Members and the Canadian Public: A Stated-Preferences Comparison
by C. Skedgel
Curr. Oncol. 2016, 23(5), 322-328; https://doi.org/10.3747/co.23.3033 - 01 Oct 2016
Cited by 8 | Viewed by 420
Abstract
The pan-Canadian Oncology Drug Review (PCODR) is responsible for making coverage recommendations to provincial and territorial drug plans about cancer drugs. Within the pcodr process, small groups of experts (including public representatives) consider the characteristics of each drug and make a funding recommendation. [...] Read more.
The pan-Canadian Oncology Drug Review (PCODR) is responsible for making coverage recommendations to provincial and territorial drug plans about cancer drugs. Within the pcodr process, small groups of experts (including public representatives) consider the characteristics of each drug and make a funding recommendation. It is important to understand how the values and preferences of those decision-makers compare with the values and preferences of the citizens on whose behalf they are acting. In the present study, stated preference methods were used to elicit prioritization preferences from a representative sample of the Canadian public and a small convenience sample of pcodr committee members. The results suggested that neither group sought strictly to maximize quality-adjusted life year (OALY) gains and that they were willing to sacrifice some efficiency to prioritize particular patient characteristics. Both groups had a significant aversion to prioritizing older patients, patients in good pre-treatment health, and patients in poor post-treatment health. Those results are reassuring, in that they suggest that pcodr decision-maker preferences are consistent with those of the Canadian public, but they also imply that, like the larger public, decision-makers might value health gains to some patients more or less highly than the same gains to others. The implicit nature of pcodr decision criteria means that the acceptability or limits of such differential valuations are unclear. Likewise, there is no guidance as to which potential equity factors—for example, age, initial severity, and so on—are legitimate and which are not. More explicit guidance could improve the consistency and transparency of pcodr recommendations. Full article
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Reoperation Costs in Attempted Breast-Conserving Surgery: A Decision Analysis
by R.E. Pataky and C.R. Baliski
Curr. Oncol. 2016, 23(5), 314-321; https://doi.org/10.3747/co.23.2989 - 01 Oct 2016
Cited by 37 | Viewed by 674
Abstract
Background: Breast-conserving surgery (BCS) is the preferred surgical approach for most patients with early-stage breast cancer. Frequently, concerns arise about the pathologic margin status, resulting in an average reoperation rate of 23% in Canada. No consensus has been reached about the [...] Read more.
Background: Breast-conserving surgery (BCS) is the preferred surgical approach for most patients with early-stage breast cancer. Frequently, concerns arise about the pathologic margin status, resulting in an average reoperation rate of 23% in Canada. No consensus has been reached about the ideal reoperation rate, although 10% has been suggested as a target. Upon undergoing reoperation, many patients choose mastectomy and breast reconstruction, which add to the morbidity and cost of patient care. We attempted to identify the cost of reoperation after BCS, and the effect that a reduction in the reoperation rate could have on the B.C. health care system. Methods: A decision tree was constructed to estimate the average cost per patient undergoing initial BCS with two reoperation frequency scenarios: 23% and 10%. The model included the direct medical costs from the perspective of the B.C. health care system for the most common surgical treatment options, including breast reconstruction and postoperative radiation therapy. Results: Costs ranged from a low of $8,225 per patient with definitive BCS [95% confidence interval (CI): $8,061 to $8,383] to a high of $26,026 for reoperation with mastectomy and delayed reconstruction (95% CI: $23,991 to $28,122). If the reoperation rate could be reduced to 10%, the average saving would be $1,055 per patient undergoing attempted BCS (95% CI: $959 to $1,156). If the lower rate were to be achieved in British Columbia, it would translate into a savings of $1.9 million annually. Summary: The implementation of initiatives to reduce reoperation after BCS could result in significant savings to the health care system, while potentially improving the quality of patient care. Full article
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A Time-and-Motion Approach to Micro-Costing of High-Throughput Genomic Assays
by S. Costa, D.A. Regier, B. Meissner, I. Cromwell, S. Ben-Neriah, E. Chavez, S. Hung, C. Steidl, D.W. Scott, M.A. Marra, S.J. Peacock and J.M. Connors
Curr. Oncol. 2016, 23(5), 304-313; https://doi.org/10.3747/co.23.2987 - 01 Oct 2016
Cited by 12 | Viewed by 707
Abstract
Background: Genomic technologies are increasingly used to guide clinical decision-making in cancer control. Economic evidence about the cost-effectiveness of genomic technologies is limited, in part because of a lack of published comprehensive cost estimates. In the present micro-costing study, we used a time-and-motion [...] Read more.
Background: Genomic technologies are increasingly used to guide clinical decision-making in cancer control. Economic evidence about the cost-effectiveness of genomic technologies is limited, in part because of a lack of published comprehensive cost estimates. In the present micro-costing study, we used a time-and-motion approach to derive cost estimates for 3 genomic assays and processes—digital gene expression profiling (GEP), fluorescence in situ hybridization (FISH), and targeted capture sequencing, including bioinformatics analysis—in the context of lymphoma patient management. Methods: The setting for the study was the Department of Lymphoid Cancer Research laboratory at the BC Cancer Agency in Vancouver, British Columbia. Mean per-case hands-on time and resource measurements were determined from a series of direct observations of each assay. Per-case cost estimates were calculated using a bottom-up costing approach, with labour, capital and equipment, supplies and reagents, and overhead costs included. Results: The most labour-intensive assay was found to be FISH at 258.2 minutes per case, followed by targeted capture sequencing (124.1 minutes per case) and digital GEP (14.9 minutes per case). Based on a historical case throughput of 180 cases annually, the mean per-case cost (2014 Canadian dollars) was estimated to be $1,029.16 for targeted capture sequencing and bioinformatics analysis, $596.60 for FISH, and $898.35 for digital GEP with an 807-gene code set. Conclusions: With the growing emphasis on personalized approaches to cancer management, the need for economic evaluations of high-throughput genomic assays is increasing. Through economic modelling and budget-impact analyses, the cost estimates presented here can be used to inform priority-setting decisions about the implementation of such assays in clinical practice. Full article
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Association between Basal-Like Phenotype and BRCA1/2 Germline Mutations in Korean Breast Cancer Patients
by J. Jung, E. Kang, J.M. Gwak, A.N. Seo, S.Y. Park, A.S. Lee, H. Baek, S. Chae, E.K. Kim and S.W. Kim
Curr. Oncol. 2016, 23(5), 298-303; https://doi.org/10.3747/co.23.3054 - 01 Oct 2016
Cited by 7 | Viewed by 688
Abstract
Introduction: BRCA mutation testing allows index patients and their families to be provided with appropriate cancer risk-reduction strategies. Because of the low prevalence of BRCA mutations in unselected breast cancer patients and the high cost of genetic testing, it is important to identify [...] Read more.
Introduction: BRCA mutation testing allows index patients and their families to be provided with appropriate cancer risk-reduction strategies. Because of the low prevalence of BRCA mutations in unselected breast cancer patients and the high cost of genetic testing, it is important to identify the subset of women who are likely to carry BRCA mutations. In the present study, we examined the association between BRCA1/2 germline mutations and the immunohistochemical features of breast cancer. Methods: In a retrospective review of 498 breast cancer patients who had undergone BRCA testing at Seoul National University Bundang Hospital between July 2003 and September 2012, we gathered immunohistochemical information on estrogen receptor (ER), progesterone receptor (PR), HER2 (human epidermal growth factor receptor 2), cytokeratin 5/6, EGFR (epidermal growth factor receptor), and p53 status. Results: Among the 411 patients eligible for the study, 50 (12.2%) had germline mutations in BRCA1 or BRCA2. Of the 93 patients with triple-negative breast cancer (TNBC), 25 with BRCA1/2 mutations were identified (BRCA1, 20.4%; BRCA2, 6.5%). On univariate analysis, ER, PR, cytokeratin 5/6, EGFR, and TNBC were found to be related to BRCA1 mutations, but on multivariate analysis, only TNBC was significantly associated with BRCA1 mutations. Among patients with early-onset breast cancer or with a family history of breast or ovarian cancer, BRCA1 mutations were significantly more prevalent in the tnbc group than in the non-TNBC group. Conclusions: In the present study, TNBC was the only independent predictor of BRCA1 mutation in patients at high risk of hereditary breast and ovarian cancers. Other histologic features of basal-like breast cancer did not improve the estimate of BRCA1 mutation risk. Full article
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Article
Do Acronyms Belong in the Medical Literature? A Countercurrents Seriesa
by S.A. Narod, H. Ahmed and M.R. Akbari
Curr. Oncol. 2016, 23(5), 295-296; https://doi.org/10.3747/co.23.3122 - 01 Oct 2016
Cited by 4 | Viewed by 494
Abstract
After controlling for ds, rd, an interaction term for ds/cs, [...] Full article
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