TY  - JOUR
ID  - discovery10151872
N2  - Definitions of platinum resistance have been questioned and changed over the last five years, even though no predictive biomarker of resistance exists. These have sculpted how we approach platinum retreatment and, consequently, how we devise new treatment strategies for those patients with tumour progression on platinum therapy. Platinum-non-eligible ovarian cancer is treated with single-agent non-platinum drugs. When bevacizumab can be added to chemotherapy, progression-free survival improves significantly. For patients with a BRCA mutation, PARP inhibitor monotherapy is an option compared to chemotherapy. There is currently no clearly identified role for immune-checkpoint inhibition in this patient population. This review describes some of the challenges in treating patients with platinum resistance and suggests refinements in the selection of patients most likely to benefit from targeting a DNA damage response, angiogenesis or immune modulation. It also describes novel agents of interest and possible mechanisms of the synergy of therapeutic combinations.
PB  - OAE Publishing Inc.
KW  - DNA damage response
KW  -  PARP inhibitors
KW  -  Platinum resistance
KW  -  VEGF inhibitors
KW  -  immune checkpoint inhibitors
TI  - Ovarian cancer recurrence: is the definition of platinum resistance modified by PARPi and other intervening treatments? The evolving landscape in the management of platinum-resistant ovarian cancer
EP  - 435
AV  - public
Y1  - 2022/05/12/
UR  - https://dx.doi.org/10.20517/cdr.2022.13
JF  - Cancer Drug Resistance
A1  - Flynn, Michael J
A1  - Ledermann, Jonathan A
SP  - 424
VL  - 5
N1  - © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
IS  - 2
ER  -