CONCLUSIONS AND FUTURE DIRECTIONS
The approval of docetaxel chemotherapy in prostate cancer treatment ushered in an era in which improvement in OS became a well-defined, achievable end point. However, resistance still occurs, and responses are limited in men with mCRPC. There is a continuing need to understand varying mechanisms of resistance and ways to overcome them. In order to better understand tumor biology and mechanisms of chemoresistance, pre- and postchemotherapy molecular analyses of tumor genomic material are critical. Additionally, the mechanisms of resistance to chemotherapy following administration of other classes of agents, such as anti-androgen agents, may also be applicable considering the cross-resistance between them. Rational selection of patients is also important to produce large increments and to develop precision medicine.
ACADEMIC EDITOR: William Chi-shing Cho, Editor in Chief
PEER REVIEW: Ten peer reviewers contributed to the peer review report. Reviewers’ reports totaled 1840 words, excluding any confidential comments to the academic editor.
FUNDING: Guru Sonpavde gratefully acknowledges the research support extended to Department of Medicine, University of Alabama at Birmingham, by Onyx, Bayer, Boehringer-Ingelheim, Merck, Sanofi, Celgene, and Pfizer. The authors confirm that the funder had no influence over the study design, content of the article, or selection of this journal.
COMPETING INTERESTS: VL is an advisory board member for aHUS for Alexion. JBA-C is an advisory board member for Dendreon, Algeta/Bayer and AZD, and a member of the speakers’ bureau for BMS. GS discloses research support to his institution from Onyx, Bayer, Boehringer-Ingleheim, Merck, Sanofi, Celgene and Pfizer. GS is a consultant to Bayer, Pfizer, Novartis, Sanofi, Genentech, Agensys, Argos, Astrazeneca, Janssen and Eisai, and a speaker and author for Clinical Care Options and Uptodate.
Paper subject to independent expert blind peer review. All editorial decisions made by independent academic editor. Upon submission manuscript was subject to anti-plagiarism scanning. Prior to publication all authors have given signed confirmation of agreement to article publication and compliance with all applicable ethical and legal requirements, including the accuracy of author and contributor information, disclosure of competing interests and funding sources, compliance with ethical requirements relating to human and animal study participants, and compliance with any copyright requirements of third parties. This journal is a member of the Committee on Publication Ethics (COPE).
Vipin Lohiya,1 Jeanny B. Aragon-Ching,2 and Guru Sonpavde1
1Division of Hematology-Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
2INOVA Schar Cancer Institute, Fairfax, VA, USA.
CORRESPONDENCE: Email: [email protected]
Conceived and designed the experiments: GS, VL, JA. Analyzed the data: GS, VL, JA. Wrote the first draft of the manuscript: VL. Contributed to the writing of the manuscript: GS, VL, JA. Agree with manuscript results and conclusions: GS, VL, JA. Jointly developed the structure and arguments for the paper: GS, VL, JA. Made critical revisions and approved final version: GS, VL, JA. All authors reviewed and approved of the final manuscript.
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