University Hospitals Leuven, Department of Obstetrics and Gynaecology, Leuven, Belgium.
European Organisation for Research and Treatment of Cancer, Gynecological Cancer Group, Brussels, Belgium.
Lancet Oncol. 2018 Dec;19(12):1680-1687. doi: 10.1016/S1470-2045(18)30566-7. Epub 2018 Nov 6.
Individual patient data from two randomised trials comparing neoadjuvant chemotherapy with upfront debulking surgery in advanced tubo-ovarian cancer were analysed to examine long-term outcomes for patients and to identify any preferable therapeutic approaches for subgroup populations.
We did a per-protocol pooled analysis of individual patient data from the European Organisation for Research and Treatment of Cancer (EORTC) 55971 trial (NCT00003636) and the Medical Research Council Chemotherapy Or Upfront Surgery (CHORUS) trial (ISRCTN74802813). In the EORTC trial, eligible women had biopsy-proven International Federation of Gynecology and Obstetrics (FIGO) stage IIIC or IV invasive epithelial tubo-ovarian carcinoma. In the CHORUS trial, inclusion criteria were similar to those of the EORTC trial, and women with apparent FIGO stage IIIA and IIIB disease were also eligible. The main aim of the pooled analysis was to show non-inferiority in overall survival with neoadjuvant chemotherapy compared with upfront debulking surgery, using the reverse Kaplan-Meier method. Tests for heterogeneity were based on Cochran's Q heterogeneity statistic.
Data for 1220 women were included in the pooled analysis, 670 from the EORTC trial and 550 from the CHORUS trial. 612 women were randomly allocated to receive upfront debulking surgery and 608 to receive neoadjuvant chemotherapy. Median follow-up was 7·6 years (IQR 6·0-9·6; EORTC, 9·2 years [IQR 7·3-10·4]; CHORUS, 5·9 years [IQR 4·3-7·4]). Median age was 63 years (IQR 56-71) and median size of the largest metastatic tumour at diagnosis was 8 cm (IQR 4·8-13·0). 55 (5%) women had FIGO stage II-IIIB disease, 831 (68%) had stage IIIC disease, and 230 (19%) had stage IV disease, with staging data missing for 104 (9%) women. In the entire population, no difference in median overall survival was noted between patients who underwent neoadjuvant chemotherapy and upfront debulking surgery (27·6 months [IQR 14·1-51·3] and 26·9 months [12·7-50·1], respectively; hazard ratio [HR] 0·97, 95% CI 0·86-1·09; p=0·586). Median overall survival for EORTC and CHORUS patients was significantly different at 30·2 months (IQR 15·7-53·7) and 23·6 months (10·5-46·9), respectively (HR 1·20, 95% CI 1·06-1·36; p=0·004), but was not heterogeneous (Cochran's Q, p=0·17). Women with stage IV disease had significantly better outcomes with neoadjuvant chemotherapy compared with upfront debulking surgery (median overall survival 24·3 months [IQR 14·1-47·6] and 21·2 months [10·0-36·4], respectively; HR 0·76, 95% CI 0·58-1·00; p=0·048; median progression-free survival 10·6 months [7·9-15·0] and 9·7 months [5·2-13·2], respectively; HR 0·77, 95% CI 0·59-1·00; p=0·049).
Long-term follow-up data substantiate previous results showing that neoadjuvant chemotherapy and upfront debulking surgery result in similar overall survival in advanced tubo-ovarian cancer, with better survival in women with stage IV disease with neoadjuvant chemotherapy. This pooled analysis, with long-term follow-up, shows that neoadjuvant chemotherapy is a valuable treatment option for patients with stage IIIC-IV tubo-ovarian cancer, particularly in patients with a high tumour burden at presentation or poor performance status.
National Cancer Institute and Vlaamse Liga tegen kanker (Flemish League against Cancer).
对比较新辅助化疗与前期肿瘤减灭术在晚期卵巢上皮性癌中疗效的两项随机试验的个体患者数据进行分析,旨在评估患者的长期预后,并确定亚组人群的更佳治疗方法。
我们对欧洲癌症研究与治疗组织(EORTC)55971 试验(NCT00003636)和英国医学研究理事会化疗或前期肿瘤减灭术(CHORUS)试验(ISRCTN74802813)的个体患者数据进行了按方案的汇总分析。EORTC 试验中,入组患者为经组织学证实的国际妇产科联盟(FIGO)分期 IIIC 或 IV 期侵袭性上皮性卵巢癌。CHORUS 试验的纳入标准与 EORTC 试验相似,FIGO 分期 IIIA 和 IIIB 期的患者也符合入组条件。汇总分析的主要目的是使用反向 Kaplan-Meier 法证明与前期肿瘤减灭术相比,新辅助化疗在总生存期方面非劣效性,异质性检验基于 Cochran's Q 异质性统计量。
1220 名女性的数据纳入了汇总分析,其中 670 名来自 EORTC 试验,550 名来自 CHORUS 试验。612 名女性随机分配接受前期肿瘤减灭术,608 名接受新辅助化疗。中位随访时间为 7.6 年(IQR 6.0-9.6;EORTC 试验为 9.2 年 [IQR 7.3-10.4];CHORUS 试验为 5.9 年 [IQR 4.3-7.4])。中位年龄为 63 岁(IQR 56-71),诊断时最大转移性肿瘤的中位大小为 8 cm(IQR 4.8-13.0)。55 名(5%)女性为 FIGO 分期 II-IIIB 期,831 名(68%)为 IIIC 期,230 名(19%)为 IV 期,104 名(9%)女性的分期数据缺失。在整个人群中,接受新辅助化疗与前期肿瘤减灭术的患者的中位总生存期无差异(27.6 个月 [IQR 14.1-51.3]与 26.9 个月 [12.7-50.1],风险比 [HR] 0.97,95% CI 0.86-1.09;p=0.586)。EORTC 和 CHORUS 患者的中位总生存期明显不同,分别为 30.2 个月(IQR 15.7-53.7)和 23.6 个月(IQR 10.5-46.9)(HR 1.20,95% CI 1.06-1.36;p=0.004),但无显著异质性(Cochran's Q,p=0.17)。与前期肿瘤减灭术相比,IV 期疾病患者接受新辅助化疗的预后明显更好(中位总生存期分别为 24.3 个月 [IQR 14.1-47.6]和 21.2 个月 [10.0-36.4],HR 0.76,95% CI 0.58-1.00;p=0.048;中位无进展生存期分别为 10.6 个月 [7.9-15.0]和 9.7 个月 [5.2-13.2],HR 0.77,95% CI 0.59-1.00;p=0.049)。
长期随访数据证实了先前的结果,即新辅助化疗与前期肿瘤减灭术在晚期卵巢上皮性癌中疗效相似,IV 期疾病患者的生存率更高。这项具有长期随访的汇总分析表明,新辅助化疗是 IIIC-IV 期卵巢上皮性癌患者的一种有价值的治疗选择,尤其是在初次就诊时肿瘤负荷较高或表现状态较差的患者中。
美国国立癌症研究所和弗拉芒语癌症协会(Vlaamse Liga tegen kanker)。