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广泛期小细胞支气管肺癌:采用大剂量环磷酰胺加大剂量依托泊苷进行强化诱导化疗。

Extensive-stage small-cell bronchogenic carcinoma: intensive induction chemotherapy with high-dose cyclophosphamide plus high-dose etoposide.

作者信息

Johnson D H, Wolff S N, Hainsworth J D, Porter L L, Grosh W W, Hande K R, Greco F A

出版信息

J Clin Oncol. 1985 Feb;3(2):170-5. doi: 10.1200/JCO.1985.3.2.170.

Abstract

Seventeen ambulatory patients with extensive-stage small-cell lung cancer received one or two courses of high-dose induction chemotherapy consisting of cyclophosphamide (100 mg/kg) plus etopside (1,200 mg/m2) followed by four or five cycles of conventional-dose cyclophosphamide (1,000 mg/m2), doxorubicin (40 mg/m2), and vincristine (1.4 mg/m2) (CAV) given every 21 days. No additional chemotherapy was given until relapse or progression was documented. Response was assessed initially after high-dose induction therapy and again after completion of all chemotherapy. After induction therapy, 16/17 (94%) patients had achieved an objective response, including five (29%) complete responses and 11 (65%) partial responses. Two partially responding patients improved to a complete response after CAV, while one partial responder progressed and one patient died of an intercurrent illness while receiving CAV. Thus, the overall response after completing all chemotherapy was 15/16 (94%), including seven (44%) complete responses and eight (50%) partial responses. Median response duration was six months (range, 3 to 11 months), and overall median survival was ten months (range, 2 to 17 months). All 31 courses of induction therapy were associated with leukopenia (less than 1,000/microL), 81% with thrombocytopenia (less than 20,000/microL), and 77% with fever (greater than 38.5 degrees C). Seven episodes of bacteremia and one axillary abscess were documented, and there was one treatment-related death (6%). These toxicities are similar to that produced by high-dose etoposide alone. High-dose cyclophosphamide combined with high-dose etoposide can be administered to ambulatory patients with extensive-stage small-cell lung cancer without requiring bone marrow transplantation to reestablish hematopoiesis. Complete response and median survival rates, however, are similar to those obtained with less intensive therapy.

摘要

17例广泛期小细胞肺癌门诊患者接受了一或两个疗程的高剂量诱导化疗,化疗方案为环磷酰胺(100mg/kg)加依托泊苷(1200mg/m²),随后每21天接受四或五个疗程的常规剂量环磷酰胺(1000mg/m²)、阿霉素(40mg/m²)和长春新碱(1.4mg/m²)(CAV方案)。在记录到复发或进展之前不再给予额外化疗。在高剂量诱导治疗后及所有化疗完成后分别评估疗效。诱导治疗后,17例患者中有16例(94%)获得客观缓解,包括5例(29%)完全缓解和11例(65%)部分缓解。2例部分缓解患者在接受CAV方案后改善为完全缓解,1例部分缓解患者病情进展,1例患者在接受CAV方案时死于并发疾病。因此,完成所有化疗后的总缓解率为16例中的15例(94%),包括7例(44%)完全缓解和8例(50%)部分缓解。中位缓解持续时间为6个月(范围3至11个月),总体中位生存期为10个月(范围2至17个月)。所有31个疗程的诱导治疗均伴有白细胞减少(低于1000/μL),81%伴有血小板减少(低于20000/μL),77%伴有发热(高于38.5℃)。记录到7次菌血症发作和1例腋窝脓肿,有1例与治疗相关的死亡(6%)。这些毒性反应与单独使用高剂量依托泊苷产生的毒性反应相似。高剂量环磷酰胺联合高剂量依托泊苷可用于广泛期小细胞肺癌门诊患者,无需进行骨髓移植来重建造血功能。然而,完全缓解率和中位生存率与强度较低的治疗相似。

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