Topic Editors

1. EPI Unit-Instituto de Saúde Pública, Universidade do Porto, Rua das Taipas, 135, 4050-600 Porto, Portugal
2. Laboratório para a Investigação Integrativa e Translacional em Saúde Populacional (ITR), Rua das Taipas, 135, 4050-600 Porto, Portugal
3. Departamento de Ciências da Saúde Pública e Forenses e Educação Médica, Faculdade de Medicina da Universidade do Porto, Alameda Professor Hernâni Monteiro, 4200-319 Porto, Portugal
EPIUnit—Instituto de Saúde Pública, Universidade do Porto, Rua das Taipas 135, 4050-600 Porto, Portugal
Dr. Samantha Morais
1. ICES, Toronto, ON M4N 3M5, Canada
2. EPI Unit-Instituto de Saúde Pública, Universidade do Porto, Rua das Taipas, 135, 4050-600 Porto, Portugal

Life of Cancer Survivor

Abstract submission deadline
21 October 2024
Manuscript submission deadline
24 December 2024
Viewed by
4737

Topic Information

Dear Colleagues,

Early tumor detection strategies, effective treatments, and follow-up care have contributed to increased cancer survival, although optimal cancer care will always need to be updated in light of new evidence, and disparities between and within countries still need to be addressed. From acute to extended and permanent survival, patients living after their cancer diagnosis face treatment and its acute, long-term, and late complications, uncertainties, fears, and loneliness. While feeling different with cancer sequelae, they struggle to return to an enjoyable life with a job or pursuing education, living with family, friends, and the whole of society. In addition to adapting to post-cancer life and changes in life perspectives and relationships, how society responds to a cancer survivor may also lead to increased difficulties for cancer survivors, namely cancer-related stigma and financial problems. In young cancer survivors, the negative effects of cancer treatments on sexual life and fertility can also affect the possibility of having children. This topic aims to gather research studies on cancer's consequences on different life dimensions of cancer survivors.

Dr. Nuno Lunet
Dr. Natália Araújo
Dr. Samantha Morais
Topic Editors

Keywords

  • cancer survivors
  • patient-reported outcomes
  • quality of care
  • second primary cancers
  • non-fatal cancer outcomes

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Cancers
cancers
5.2 7.4 2009 17.9 Days CHF 2900 Submit
Current Oncology
curroncol
2.6 2.6 1994 18 Days CHF 2200 Submit
Healthcare
healthcare
2.8 2.7 2013 19.5 Days CHF 2700 Submit
Nursing Reports
nursrep
2.4 1.6 2011 30.6 Days CHF 1800 Submit
Onco
onco
- - 2021 18.3 Days CHF 1000 Submit

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Published Papers (4 papers)

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20 pages, 731 KiB  
Case Report
Actuarial Analysis of Survival after Breast Cancer Diagnosis among Lithuanian Females
by Justina Levickytė, Aldona Skučaitė, Jonas Šiaulys, Rokas Puišys and Ieva Vincerževskienė
Healthcare 2024, 12(7), 746; https://doi.org/10.3390/healthcare12070746 - 29 Mar 2024
Viewed by 431
Abstract
Breast cancer is the most common cause of mortality due to cancer for women both in Lithuania and worldwide. The chances of survival after diagnosis differ significantly depending on the stage of disease at the time of diagnosis and other factors. One way [...] Read more.
Breast cancer is the most common cause of mortality due to cancer for women both in Lithuania and worldwide. The chances of survival after diagnosis differ significantly depending on the stage of disease at the time of diagnosis and other factors. One way to estimate survival is to construct a Kaplan–Meier estimate for each factor value separately. However, in cases when it is impossible to observe a large number of patients (for example, in the case of countries with lower numbers of inhabitants), dividing the data into subsets, say, by stage at diagnosis, may lead to results where some subsets contain too few data, thus causing the results of a Kaplan–Meier (or any other) method to become statistically incredible. The problem may become even more acute if researchers want to use more risk factors, such as stage at diagnosis, sex, place of living, treatment method, etc. Alternatively, Cox models can be used to analyse survival data with covariates, and they do not require the data to be divided into subsets according to chosen risks factors (hazards). We estimate the chances of survival for up to 5 years after a breast cancer diagnosis for Lithuanian females during the period of 1995–2016. Firstly, we construct Kaplan-Meier estimates for each stage separately; then, we apply a (stratified) Cox model using stage, circumstance of diagnosis, and year of diagnosis as (potential) hazards. Some directions of further research are provided in the last section of the paper. Full article
(This article belongs to the Topic Life of Cancer Survivor)
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15 pages, 291 KiB  
Article
Psychological Distress and Concerns of In-Home Older People Living with Cancer and Their Impact on Supportive Care Needs: An Observational Survey
by Christos Kleisiaris, Maria Maniou, Savvato Karavasileiadou, Constantinos Togas, Theocharis Konstantinidis, Ioanna V. Papathanasiou, Konstantinos Tsaras, Wafa Hamad Almegewly, Emmanouil Androulakis and Hanan Hamdan Alshehri
Curr. Oncol. 2023, 30(11), 9569-9583; https://doi.org/10.3390/curroncol30110692 - 31 Oct 2023
Viewed by 1302
Abstract
(1) Background: Cancer patients are experiencing psychological problems after diagnosis, such as emotional distress and social anxiety, which may increase their demands for emotional and supportive care. This study aimed to assess the influence of both emotional distress and concerns on the supportive [...] Read more.
(1) Background: Cancer patients are experiencing psychological problems after diagnosis, such as emotional distress and social anxiety, which may increase their demands for emotional and supportive care. This study aimed to assess the influence of both emotional distress and concerns on the supportive care needs of cancer patients receiving home-based healthcare. (2) Methods: In this door-to-door screening program, 97 cancer patients were approached, with a mean age of 73 years old (mean = 73.43; SD = 6.60). (3) Results: As expected, 42.3% of patients highlighted their treatment as their main psychological priority, with 20.6% identifying concerns about the future of their family in this regard. No significant associations with respect to sex were identified in terms of focus, though females reported the need for more frequent psychological support (58.7% vs. 37.3%, respectively, p = 0.035) compared to males. Patients who had experienced an increased number of concerns during the last weeks (IRR = 1.02; 95% CI: 1.00–1.03, p = 0.007) had a significantly greater risk of presenting an increased rate of supportive care needs. Notably, male patients with bone cancer presented a significantly greater number of supportive care needs (mean rank 45.5 vs. 9.0, p = 0.031) respectively, in comparison to those with other types of cancer. (4) Conclusions: Supportive care needs arise from a greater concern and specific type of cancer, highlighting the need for supportive care, such as psychosocial and psychological support. This may have significant implications for treatment and patient outcomes in home care settings. Full article
(This article belongs to the Topic Life of Cancer Survivor)
11 pages, 301 KiB  
Article
Pretreatment Cancer-Related Cognitive Impairment in Hodgkin Lymphoma Patients
by Veronika Juríčková, Dan Fayette, Juraj Jonáš, Iveta Fajnerová, Tomáš Kozák and Jiří Horáček
Curr. Oncol. 2023, 30(10), 9028-9038; https://doi.org/10.3390/curroncol30100652 - 05 Oct 2023
Viewed by 1296
Abstract
Background: Cancer-related cognitive impairment (CRCI) is one of the most serious side effects of cancer that negatively impacts the quality of life of cancer patients and survivors. There is evidence of CRCI in Hodgkin lymphoma patients (HL); however, there is a lack of [...] Read more.
Background: Cancer-related cognitive impairment (CRCI) is one of the most serious side effects of cancer that negatively impacts the quality of life of cancer patients and survivors. There is evidence of CRCI in Hodgkin lymphoma patients (HL); however, there is a lack of studies examining the presence of cognitive deficits before starting any treatment in HL patients. Methods: Forty adult patients (N = 40) newly diagnosed with HL (with no previous cancer diagnoses) and 40 healthy controls (N = 40) matched for age, sex, education, and premorbid intellect completed the neuropsychological battery and subjective and objective measures of affective distress and quality of life. Results: The results showed impairment in three out of six cognitive domains: verbal memory and learning, speed of processing/psychomotor speed, and abstraction/executive functions in the HL patients before the initiation of any treatment. The speed of processing/psychomotor speed domain is negatively correlated with depression. Conclusion: Cognitive deterioration in verbal memory and learning and abstraction/executive functions domains in HL patients seems to occur before the initiation of treatment independently of anxiety, depression, or physical symptoms. This suggests that HL itself may cause cognitive deficits in these cognitive domains. However, the underlying causes of CRCI still remain unclear. Full article
(This article belongs to the Topic Life of Cancer Survivor)
16 pages, 1842 KiB  
Article
Prioritizing Solutions and Improving Resources among Young Pediatric Brain Tumor Survivors: Results of an Online Survey
by Marco Bonanno, Claude Julie Bourque, Lye-Ann Robichaud, Ariane Levesque, Ariane Lacoste-Julien, Émélie Rondeau, Émilie Dubé, Michelle Leblanc, Marie-Claude Bertrand, Carole Provost, Leandra Desjardins and Serge Sultan
Curr. Oncol. 2023, 30(9), 8586-8601; https://doi.org/10.3390/curroncol30090623 - 19 Sep 2023
Cited by 1 | Viewed by 1128
Abstract
Pediatric Brain Tumor Survivors (PBTS) often experience social, academic and employment difficulties during aftercare. Despite their needs, they often do not use the services available to them. Following a previous qualitative study, we formulated solutions to help support PBTS return to daily activities [...] Read more.
Pediatric Brain Tumor Survivors (PBTS) often experience social, academic and employment difficulties during aftercare. Despite their needs, they often do not use the services available to them. Following a previous qualitative study, we formulated solutions to help support PBTS return to daily activities after treatment completion. The present study aims to confirm and prioritize these solutions with a larger sample. We used a mixed-methods survey with 68 participants (43 survivors, 25 parents, PBTS’ age: 15–39 years). Firstly, we collected information about health condition, and school/work experience in aftercare. Then, we asked participants to prioritize the previously identified solutions using Likert scales and open-ended questions. We used descriptive and inferential statistics to analyze data, and qualitative information to support participants’ responses. Participants prioritized the need for evaluation, counseling, and follow-up by health professionals to better understand their post-treatment needs, obtain help to access adapted services, and receive information about resources at school/work. Responses to open-ended questions highlighted major challenges regarding the implementation of professionals’ recommendations at school/work and the need for timely interventions. These results will help refine solutions for PBTS and provide key elements for future implementation. Translating these priorities into action will need further work involving professionals and decision makers. Full article
(This article belongs to the Topic Life of Cancer Survivor)
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