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Review
Peer-Review Record

How Far Have We Developed Antibody–Drug Conjugate for the Treatment of Cancer?

Drugs Drug Candidates 2023, 2(2), 377-421; https://doi.org/10.3390/ddc2020020
by Yu Jun Lim 1, Pei Sze Clarissa Lau 1, Shi Xuan Low 1, Shong Li Ng 1, Min Yee Ong 1, Huey Ming Pang 1, Zheng Yang Lee 1, Hui Yin Yow 2, Sharina Binti Hamzah 1, Renukha Sellappans 1 and Jhi Biau Foo 1,*
Reviewer 2:
Reviewer 3:
Drugs Drug Candidates 2023, 2(2), 377-421; https://doi.org/10.3390/ddc2020020
Submission received: 22 December 2022 / Revised: 14 February 2023 / Accepted: 11 April 2023 / Published: 23 May 2023
(This article belongs to the Section Biologics)

Round 1

Reviewer 1 Report

The review does not report substantial novelty regarding other  reviews published recently that, of course,  are not included in the reference list such as:

"An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy" 10.3390/molecules26195847

"Antibody drug conjugate: the “biological missile” for targeted cancer therapy" 10.1038/s41392-022-00947-7

“Antibody–Drug Conjugates: The Last Decade” 10.3390/ph13090245

In addition, I would suggest the authors to be more careful drawing the molecular structures they did not follow a fixed style and everyone has a different size.

 

Author Response

Please see the attachment

Author Response File: Author Response.docx

Reviewer 2 Report

This paper reviewed the principles of antibody-drug conjugates (ADCs) and the ADCs in clinic, under development and that discontinued/terminated in clinical trials. Additionally, the challenges about the use of ADC were discussed, highlighting the further directions for ADCs improvement. The topic fits the scope of the journal and may benefit the development of ADCs for the treatment of human diseases. In general, the manuscript is well-organized and the references can support the conclusions. The key issues are required to be addressed before its publication on Drugs and Drug Candidates.

 

1. The timeline of ADCs development is suggested to be introduced with a figure illustration in the Introduction section.

2. The target features of successful ADCs are suggested to be summarized in the section 5.

3. The advantages/disadvantages of ADCs with small-molecule drugs are suggested to be compared and analyzed (probably with a table).

Author Response

Please see the attachment

Author Response File: Author Response.docx

Reviewer 3 Report

Antibody-drug conjugate for targeted cancer therapy is a promising area of research. I appreciate the authors for their efforts to assemble up-to-date information in this manuscript regarding ADC. I have the following comments for the authors -

1. I found redundant information regarding FDA-approved ADCs as this has been already published in recent review articles, such as ref. 148 (mentioned in this paper).

2. Following recent review articles are missing -

1. Potential of antibody–drug conjugates (ADCs) for cancer therapy. Hasan et al., 2022

2. Antibody drug conjugate: the “biological missile” for targeted cancer therapy. Zhang et al., 2022

3. There are many antibody-drug conjugates mentioned in table-3 but only a few have been discussed. Moreover, this list is not comprehensive as there are more ADCs in clinical development like AGS67E, AGS-62P1, MEDI4276, etc.

In my opinion including the following topics in this manuscript would make it more interesting -

1. Application of different computational techniques in addressing ADC challenges 

2. Neoantigen-targeted cancer vaccines

Author Response

Please see the attachment

Author Response File: Author Response.docx

Round 2

Reviewer 1 Report

In my opinion, there are many reviews on the same topic. Even though the authors have included some more information, I can not see a key difference. When a reader starts to read this review will not be motivated to continue since they will read same than in others reviews

Reviewer 3 Report

Now, this manuscript looks much better than the previous version and I am thankful to the authors for considering my suggestions.

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