Bozkaya Yakup, Özdemir Nuriye Yıldırım, Yazıcı Ozan, Demirci Nebi Serkan, Kurtipek Alican, Erdem Gökmen Umut, Ergün Yakup, Zengin Nurullah
Department of Medical Oncology, SBÜ Ankara Numune Education and Research Hospital, , Ankara, Turkey. Email:
Asian Pac J Cancer Prev. 2018 Jan 27;19(1):283-290. doi: 10.22034/APJCP.2018.19.1.283.
Objective: We aimed to evaluate the effectiveness of an mEOX (modified epirubicin, oxaliplatin plus capecitabine) regimen as second line therapy after failure of mDCF (modified docetaxel, cisplatin plus fluorouracil). Methods: Gastic cancer patients for whom first-line therapy was unsuccessful and who subsequently received mEOX (epirubicin 50 mg/ m2 on day 1, oxaliplatin 85 mg/m² day 1 and capecitabine twice-daily dose of 625 mg/ m2, p.o. for 2 weeks) every 3 weeks until disease progression or unacceptable toxicity, were retrospectively analyzed. Results: The study population comprised 129 cases with a median age of 55 years (range= 27-78), the majority being male (76 %). Most (75.2%) had ≥ 2 sites of metastasis. The median number of chemotherapy courses was five (range= 2–9). Forty-nine achieved a partial response and 33 showed stable disease, resulting in a ORR (overall response rate) of 38% and a DCR (disease control rate) of 63.6%. The most frequent features of grade 3-4 hematological and non-hematological toxicity were neutropenia (8.5%) and nausea/vomiting (5.4%). None of the patients suffered death due to toxicity. The median PFS was 4.7 months (95% CI, 4.1–5.3) and the OS was 7.4 months (95% CI, 6.3–8.5). On multivariate analysis, age ≥ 60 years and ECOG performance status (0-1) were independent prognostic factors affecting PFS and OS. Conslusions: In advanced gastric cancer patients, who progress after first line chemotherapy and have an ECOG performance status of 0-1, mEOX is a well tolerated triple regimen associated with a promising OS and PFS.
我们旨在评估改良表柔比星、奥沙利铂联合卡培他滨(mEOX)方案作为改良多西他赛、顺铂联合氟尿嘧啶(mDCF)方案失败后的二线治疗的有效性。方法:对一线治疗失败且随后每3周接受mEOX方案(第1天表柔比星50mg/m²,第1天奥沙利铂85mg/m²,卡培他滨每日两次,剂量625mg/m²,口服,共2周)直至疾病进展或出现不可接受的毒性的胃癌患者进行回顾性分析。结果:研究人群包括129例患者,中位年龄55岁(范围=27 - 78岁),大多数为男性(76%)。大多数(75.2%)有≥2个转移部位。化疗疗程的中位数为5个(范围=2 - 9)。49例获得部分缓解,33例疾病稳定,总缓解率(ORR)为38%,疾病控制率(DCR)为63.6%。3 - 4级血液学和非血液学毒性最常见的表现为中性粒细胞减少(8.5%)和恶心/呕吐(5.4%)。无患者因毒性死亡。中位无进展生存期(PFS)为4.7个月(95%置信区间,4.1 - 5.3),总生存期(OS)为7.4个月(95%置信区间,6.3 - 8.5)。多因素分析显示,年龄≥60岁和东部肿瘤协作组(ECOG)体能状态(0 - 1)是影响PFS和OS的独立预后因素。结论:在一线化疗后进展且ECOG体能状态为0 - 1的晚期胃癌患者中,mEOX是一种耐受性良好的三联方案,具有有前景的OS和PFS。