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Review
Peer-Review Record

Acute Myeloid Leukemia Mutations: Therapeutic Implications

Int. J. Mol. Sci. 2019, 20(11), 2721; https://doi.org/10.3390/ijms20112721
by Cristina Papayannidis *, Chiara Sartor, Giovanni Marconi, Maria Chiara Fontana, Jacopo Nanni, Gianluca Cristiano, Sarah Parisi, Stefania Paolini and Antonio Curti
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Int. J. Mol. Sci. 2019, 20(11), 2721; https://doi.org/10.3390/ijms20112721
Submission received: 28 April 2019 / Revised: 31 May 2019 / Accepted: 31 May 2019 / Published: 3 June 2019
(This article belongs to the Special Issue Advances in Molecular Biology and Targeted Therapy of Leukemias)

Round  1

Reviewer 1 Report

Authors did a great job. Authors complied the information very well and review is very informative. But it can be shortened possibly. Here are a few suggestions.

1) Title of the review is not connected to what the authors discussed in the review. They describe the molecular landscape of acute myeloid leukemia with therapeutic implications. But they give the title molecular pathway. 

2) Add some new references.

3) In conclusion, add few more lines about future perspective. 

Author Response

1) The title of the review has been changed to: 

Acute Myeloid Leukemia mutations: therapeutic implications.

Therefore, the review is focused on the main mutations described in AML, and the recently approved drugs against these mutations

2) Some new references have been added

3) Conclusion chapter has been enriched with future perspectives


Reviewer 2 Report

This review article may merit the researcher in the relevant field. However, the paper is not well-organized. In the introduction section, the authors described that four drugs have been approved by FDA but did not mention gemtuzumab ozogamicin and CPX-351, without providing any reasons. To make the situation more confusing is that the authors did not discuss the strategy to use different types of drugs based on the molecular landscape of AML. The authors should discuss their own idea how to use these different types of molecular targeting drugs to treat AML.

The paper contains several unacceptably long paragraphs. For example, the paragraph from lines 75 to 131, should be divided into several paragraphs to enhance the readability. The authors should include the table(s) summarizing clinical trials to offer the overview of the present status of the drug development for AML to the readers.

Finally, the paper contains innumerable errors in syntax and wordings, and therefore, should be extensively edited by a professional editor who is proficient in writing medical English.

Author Response

The title of the review has been modified, and the authors decided to focus on mutations of AML and their  therapeutic implications. Therefore the text has been shortened, and divided in smaller chapters. In the discussion part, the authors describe their own ideas on the introduction of these compounds in the clinical practice, as well as future perspectives.

Chapters have been shortened, and one table summarizing the most relevant trials (recently closed to enrollment or still ongoing) with drugs targeting mutations has been added

English has been reviewed by a professional editor

Round  2

Reviewer 2 Report

The review article is well-written and will merit the researchers in the relevant research fields.

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