Department of Gynaecological Oncology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway; Crown Princess Mary Cancer Care Centre, Westmead Hospital, Sydney, New South Wales, Australia.
Crown Princess Mary Cancer Care Centre, Westmead Hospital, Sydney, New South Wales, Australia; Centre for Cancer Research, The Westmead Institute for Medical Research, Sydney, New South Wales, Australia.
Gynecol Oncol. 2018 Aug;150(2):239-246. doi: 10.1016/j.ygyno.2018.05.020. Epub 2018 May 26.
The aim of this study was to compare response rates and survival in women with "platinum resistant" epithelial ovarian cancer (EOC) who received further platinum-based or non‑platinum chemotherapy for treatment at first relapse.
Patients with high-grade EOC (including fallopian tube and peritoneal cancer) of all histologies recruited to the Australian Ovarian Cancer Study (AOCS) and treated with platinum-based primary chemotherapy were included. Response to second-line chemotherapy, overall survival (OS) and survival after treatment for first progression (OS2) were determined in all histologies and separately in women with high-grade serous tumors.
Of the 341 patients classified as platinum-resistant by the 6-month threshold, 243 (71%) were treated with chemotherapy at relapse. CA-125 response rates to platinum-based chemotherapy were significantly higher compared to non‑platinum chemotherapy (51% vs 21%, P < 0.001). Among patients with a platinum-free interval (PFI) of 3-6 months, OS2 in patients treated with platinum was significantly longer compared to individuals receiving non‑platinum-based treatment (median 17.67 months, 95% CI: 14.79-20.75 vs. 10.62 months, 95% CI: 8.02-12.72, P = 0.022). The patterns were similar when restricted to patients with high-grade serous histology. In patients with PFI <3 months, there was no significant difference in response or survival according to type of second-line treatment.
Our findings further question the use of a 6-month PFI as an arbitrary threshold for subsequent treatment decision-making. Some patients considered "platinum resistant" still derive clinical benefit from platinum-based chemotherapy. Biomarkers of platinum sensitivity are needed in clinical practice to identify potential responders who should be offered re-treatment with platinum.
本研究旨在比较在首次复发时接受进一步铂类或非铂类化疗治疗的“铂耐药”上皮性卵巢癌(EOC)女性的缓解率和生存率。
纳入所有组织学类型的澳大利亚卵巢癌研究(AOCS)招募并接受铂类基础一线化疗治疗的高级别 EOC(包括输卵管和腹膜癌)患者。确定所有组织学类型和高级别浆液性肿瘤女性中二线化疗的缓解率、总生存期(OS)和首次进展后治疗的 OS2。
在根据 6 个月阈值分类为铂耐药的 341 名患者中,有 243 名(71%)在复发时接受了化疗。铂类化疗的 CA-125 缓解率明显高于非铂类化疗(51%比 21%,P<0.001)。在无铂间隔(PFI)为 3-6 个月的患者中,接受铂类治疗的患者的 OS2 明显长于接受非铂类治疗的患者(中位 17.67 个月,95%CI:14.79-20.75 与 10.62 个月,95%CI:8.02-12.72,P=0.022)。当仅限于高级别浆液性组织学类型的患者时,模式相似。在 PFI<3 个月的患者中,二线治疗类型与缓解或生存无显著差异。
我们的研究结果进一步质疑将 6 个月的 PFI 作为后续治疗决策的任意阈值。一些被认为“铂耐药”的患者仍从铂类化疗中获得临床获益。在临床实践中需要有铂类敏感性的生物标志物来识别可能受益于铂类再治疗的潜在反应者。