da Costa Alexandre A B A, Valadares Camila V, Baiocchi Glauco, Mantoan Henrique, Saito Augusto, Sanches Solange, Guimarães Andréia P, Achatz Maria Isabel W
Medical Oncology Department, A.C. Camargo Cancer Center, Sao Paulo, SP, Brazil.
Gynecology Oncology Department, A.C. Camargo Cancer Center, Sao Paulo, SP, Brazil.
Ann Surg Oncol. 2015 Dec;22 Suppl 3:S971-8. doi: 10.1245/s10434-015-4623-z. Epub 2015 May 27.
Interval debulking surgery (IDS) is an option for treating patients with advanced ovarian carcinoma. Two randomized trials have shown similar survival rates for primary debulking surgery (PDS) and IDS. One of the concerns with IDS is the potentially higher risk of inducing platinum resistance when treating patients with greater disease volume.
A retrospective review of data on 237 patients with stage IIIC and IV ovarian carcinoma who were treated at a single institution from 2000 to 2013. We analyzed the association of IDS with time to first platinum resistant relapse (TTPR); platinum-resistant disease at first relapse, defined as a platinum-free interval (PFI) after first-line chemotherapy of <6 months; and overall response rate (ORR) to chemotherapy at first platinum-sensitive relapse.
The TTPR was 60 months, and the median TTPR was longer for the PDS (80.8 months) versus IDS group (39.3 months; p = 0.012) and for patients with residual disease (RD) ≤10 mm (80.8 months) compared with those with RD >10 mm (26.1 months; p < 0.001). In the multivariate analysis, IDS [hazard ratio (HR) 1.92; p = 0.009] and RD >10 mm (HR 1.65; p < 0.001) retained an increased risk of developing platinum-resistant disease. IDS was not associated with a greater risk of PFI <6 months at first relapse, and the ORR to platinum-based chemotherapy at first platinum-sensitive relapse was 87.2 % for patients who were treated with PDS compared with 68.0 % for those who underwent IDS (p = 0.051).
IDS correlates with a higher risk of the development of platinum resistance.
间隔减瘤手术(IDS)是治疗晚期卵巢癌患者的一种选择。两项随机试验显示,初次减瘤手术(PDS)和IDS的生存率相似。IDS的一个问题是,在治疗肿瘤体积较大的患者时,诱导铂耐药的风险可能更高。
对2000年至2013年在单一机构接受治疗的237例IIIC期和IV期卵巢癌患者的数据进行回顾性分析。我们分析了IDS与首次铂耐药复发时间(TTPR)、首次复发时的铂耐药疾病(定义为一线化疗后的无铂间期(PFI)<6个月)以及首次铂敏感复发时化疗的总缓解率(ORR)之间的关联。
TTPR为60个月,PDS组(80.8个月)的中位TTPR长于IDS组(39.3个月;p = 0.012),残留病灶(RD)≤10 mm的患者(80.8个月)的中位TTPR长于RD>10 mm的患者(26.1个月;p < 0.001)。在多变量分析中,IDS(风险比(HR)1.92;p = 0.009)和RD>10 mm(HR 1.65;p < 0.001)发生铂耐药疾病的风险仍然增加。IDS与首次复发时PFI<6个月的更高风险无关,PDS治疗的患者首次铂敏感复发时铂类化疗的ORR为87.2%,而接受IDS治疗的患者为68.0%(p = 0.051)。
IDS与铂耐药发生的较高风险相关。