"Platinum resistant" ovarian cancer: What is it, who to treat and how to measure benefit?

被引:420
作者
Davis, Alison [1 ,2 ]
Tinker, Anna V. [3 ]
Friedlander, Michael [4 ]
机构
[1] Canberra Hosp, Canberra, ACT 2606, Australia
[2] Australian Natl Univ, Canberra, ACT, Australia
[3] British Columbia Canc Agcy, Vancouver Ctr, Vancouver, BC V5Z 4E6, Canada
[4] Univ New S Wales, Prince Wales Clin Sch, Sydney, NSW, Australia
关键词
Platinum resistant; Ovarian cancer; Histotype; Genotype; Treatment; PEGYLATED LIPOSOMAL DOXORUBICIN; RECURRENT EPITHELIAL OVARIAN; RANDOMIZED PHASE-III; HEAVILY PRETREATED PATIENTS; SINGLE-AGENT PACLITAXEL; STEM-CELLS; OPEN-LABEL; SPORADIC BREAST; DNA-DAMAGE; CHEMOTHERAPY;
D O I
10.1016/j.ygyno.2014.02.038
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
(")Platinum resistant" ovarian cancer was historically defined as disease recurrence within 6 months of completion of first-line platinum-based chemotherapy, although this is now more broadly applied to also include patients progressing within 6 months after multiple lines of chemotherapy. However, this definition ignores the heterogeneity and complexity of the spectrum of diseases that comprise "platinum resistant ovarian cancer" (PROC) and is innately flawed as it was initially derived using methods of detection of recurrence that would now be regarded as outdated. The outcome of patients with PROC is generally poor, with low response rates to further chemotherapy and a median survival of less than 12 months, but this is unpredictable and can be quite variable from study to study. This review outlines the complexity of PROC, examines how this impacts on the interpretation of the results of clinical trials, and explores how the definition may be improved. We also briefly describe the mechanisms of platinum resistance, the results of clinical trials to date as well as treatment options for patients with PROC and highlight the need for better methods of assessing clinical benefit in this poor prognostic sub group of patients. Crown Copyright (C) 2014 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:624 / 631
页数:8
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