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Irinotecan leucovorin and 5-fluorouracil (modified FOLFIRI) as salvage chemotherapy for frail or elderly patients with advanced gastric cancer

机译:伊立替康亚叶酸钙和5-氟尿嘧啶(改良的FOLFIRI)作为弱势或老年晚期胃癌患者的挽救性化疗

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摘要

We retrospectively evaluated the efficacy and safety of the modified FOLFIRI regimen in frail or elderly patients with advanced gastric cancer (AGC). We reviewed 24 frail [Eastern Cooperative Oncology Group performance status (ECOG PS) of 2] or elderly (65 years or over) patients with AGC who received the modified FOLFIRI regimen as salvage chemotherapy. Patients received irinotecan 150 mg/m2 and leucovorin (LV) 100 mg/m2 as a 2 h intravenous infusion, followed by 5-fluorouracil (5-FU) 2,000 mg/m2 as a 46 h continuous infusion. Among the 24 patients, 18 (75%) had an ECOG PS of 2, and 11 (45.8%) were aged 65 years or over. A total of 113 cycles were conducted, with a median number of 4 cycles per patient. A total of 3 patients achieved partial response (PR) and 8 demonstrated stable disease (SD). On an intent-to-treat basis, the overall response rate (RR) was 12.5% and the disease control rate (PR and SD) was 45.8%. The median time to progression (TTP) was 2 months [95% confidence interval (CI), 1.9–2.1 months] and the median overall survival (OS) was 5.4 months (95% CI, 4.1–6.7 months). Grade 3–4 hematological toxicities, including neutropenia, anemia and thrombocytopenia, were observed in 6 (25%), 4 (16.7%) and 1 (4.2%) patients, respectively. Additionally, 3 (12.5%) patients developed febrile neutropenia, of which 1 succumbed to pneumonia. Grade 3–4 gastrointestinal toxicities, including nausea, vomiting, diarrhea and mucositis, were observed in 3 (12.5%), 2 (8.3%), 1 (4.2%) and 1 (4.2%) patients, respectively. In conclusion, the modified FOLFIRI regimen as salvage chemotherapy for AGC patients over 65 years of age or with a poor PS was effective and acceptable. These results suggest that this regimen may be an effective option for frail or elderly patients with AGC.
机译:我们回顾性评估改良的FOLFIRI方案在体弱或老年晚期胃癌(AGC)患者中的疗效和安全性。我们回顾了接受改良FOLFIRI方案作为挽救性化疗的24例体弱[2人的东部合作肿瘤小组表现状态(ECOG PS)]或老年(65岁以上)AGC患者。静脉输注2小时后,患者接受irinotecan 150 mg / m 2 和亚叶酸(LV)100 mg / m 2 ,然后接受5-氟尿嘧啶(5-FU)2,000 mg / m 2 连续输注46小时。在24名患者中,有18名(75%)的ECOG PS为2,11名(45.8%)的年龄在65岁或以上。总共进行了113个周期,每位患者的中位数为4个周期。共有3例患者达到部分缓解(PR),8例表现出稳定的疾病(SD)。在意向性治疗的基础上,总缓解率(RR)为12.5%,疾病控制率(PR和SD)为45.8%。中位进展时间(TTP)为2个月[95%置信区间(CI),1.9-2.1个月],中位总生存期(OS)为5.4个月(95%CI,4.1-6.7个月)。分别在6(25%),4(16.7%)和1(4.2%)的患者中观察到3-4级血液学毒性,包括中性粒细胞减少,贫血和血小板减少。此外,有3名(12.5%)患者出现了发热性中性粒细胞减少症,其中1名死于肺炎。分别在3(12.5%),2(8.3%),1(4.2%)和1(4.2%)的患者中观察到了3-4级胃肠道毒性,包括恶心,呕吐,腹泻和粘膜炎。总之,对于65岁以上或PS较差的AGC患者,改良的FOLFIRI方案作为挽救性化疗是有效且可以接受的。这些结果表明,该方案对于体弱或年长的AGC患者可能是一种有效的选择。

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