Morgan Robert D, Clamp Andrew R, Zhou Cong, Saunders Geoff, Mescallado Nerissa, Welch Richard, Mitchell Claire, Hasan Jurjees, Jayson Gordon C
The Christie NHS Foundation Trust, Manchester, UK.
Manchester Cancer Research Centre, University of Manchester, Manchester, UK.
Int J Gynecol Cancer. 2019 Feb;29(2):341-345. doi: 10.1136/ijgc-2018-000067. Epub 2019 Jan 23.
Standard of care treatment for women who develop relapsed ovarian cancer includes sequential platinum- and/or paclitaxel-based chemotherapy, with reducing disease-free intervals. Once platinum resistance develops, treatment options become limited and dose-dense regimens may be offered. We report the efficacy and safety of dose-dense cisplatin with gemcitabine chemotherapy for relapsed platinum-resistant ovarian cancer.
A retrospective analysis of all patients with relapsed, platinum-resistant ovarian, primary peritoneal or fallopian tube cancer treated with cisplatin 35 mg/m of body surface area by intravenous infusion with gemcitabine 1000 mg/m of body surface area by intravenous infusion on days 1 and 8 of every 21-day treatment cycle between 1 January 2009 and 1 June 2017.
Ninety-four eligible patients had received a median of three (range one-eight) prior lines of cytotoxic therapy for relapsed ovarian cancer. Sixty patients (64%) had received ≥ 1 prior dose-dense chemotherapy regimen. Dose-dense cisplatin with gemcitabine was associated with a median progression-free survival (PFS) of 4.4 months (95% CI 3.6 to 5.3) and overall survival of 7.6 months (95% CI 5.6 to 9.6). The median PFS for dose-dense cisplatin with gemcitabine as first- (n = 34), second- (n = 42), and third-line or later (n = 18) dose-dense therapy was 4.2 (95% CI 3.2 to 5.2), 5.0 (95% CI 3.5 to 6.5), and 4.2 (95% CI 3.3 to 5.1) months respectively. The RECIST objective response rate for first-, second-, and third-line dose-dense cisplatin with gemcitabine was 23%, 14 %, and 7 % respectively. The most common grade 3 - 4 adverse events were thrombocytopenia (20%), anemia (18%), and neutropenia (14%).
Dose-dense cisplatin with gemcitabine provides modest efficacy whether it is used as a first- or subsequent line of dose-dense chemotherapy to treat relapsed platinum-resistant ovarian cancer and the toxicity is manageable with supportive measures.
复发性卵巢癌女性的标准治疗方案包括序贯使用以铂类和/或紫杉醇为基础的化疗,无病间期会逐渐缩短。一旦出现铂类耐药,治疗选择就会受限,此时可考虑给予剂量密集方案。我们报告了剂量密集顺铂联合吉西他滨化疗用于复发性铂类耐药卵巢癌的疗效和安全性。
对2009年1月1日至2017年6月1日期间所有接受治疗的复发性铂类耐药卵巢癌、原发性腹膜癌或输卵管癌患者进行回顾性分析,这些患者每21天为一个治疗周期,在第1天和第8天通过静脉输注给予体表面积35mg/m²的顺铂和体表面积1000mg/m²的吉西他滨。
94例符合条件的患者因复发性卵巢癌接受了中位数为3(范围1 - 8)线的细胞毒性化疗。60例患者(64%)接受过≥1线先前的剂量密集化疗方案。剂量密集顺铂联合吉西他滨治疗的中位无进展生存期(PFS)为4.4个月(95%CI 3.6至5.3),总生存期为7.6个月(95%CI 5.6至9.6)。剂量密集顺铂联合吉西他滨作为一线(n = 34)、二线(n = 42)和三线及后续(n = 18)剂量密集治疗的中位PFS分别为4.2(95%CI 3.2至5.2)、5.0(95%CI 3.5至6.5)和4.2(95%CI 3.3至5.1)个月。剂量密集顺铂联合吉西他滨用于一线、二线和三线治疗的RECIST客观缓解率分别为23%、14%和7%。最常见的3 - 4级不良事件为血小板减少(20%)、贫血(18%)和中性粒细胞减少(14%)。
剂量密集顺铂联合吉西他滨无论是作为一线还是后续线的剂量密集化疗用于治疗复发性铂类耐药卵巢癌,疗效都较为有限,且毒性可通过支持措施进行控制。