Kasseyet S, Astoul P, Boutin C
Department of Pulmonology, University Hospital la Conception, Mediterranean University Medical School, Marseille, France.
Cancer. 1999 Apr 15;85(8):1740-9.
Malignant pleural mesothelioma is associated with a poor prognosis because of its resistance to treatment. The authors conducted a Phase II trial in which two drugs (etoposide and 5-fluorouracil) were added to the Cancer and Leukemia Group B cisplatin-mitomycin regimen in an effort to define a more effective chemotherapy.
Forty-five patients with confirmed Stage II malignant pleural mesothelioma were prospectively enrolled in the study. Thirty-one patients received cisplatin 60 mg/m2 on Day 1, 5-fluorouracil 600 mg on Days 1-4, folinic acid 100 mg/m2 on Days 1-4, mitomycin C 10 mg/m2 on Day 3, and etoposide 100 mg/m2 i.v. on Days 1-3, with prophylactic hematopoietic growth factors. Fourteen patients received cisplatin, 5-fluorouracil, folinic acid, and mitomycin C with the protocol unchanged, and oral etoposide 50 mg on Days 1-21 without growth factors (1 cycle every 28 days). Histology included epithelial (in 33 cases), sarcomatous (in 6), mixed (in 3), and unspecified type (in 3).
Two hundred eleven cycles were administered. Treatment was well tolerated and the major toxicity was hematologic: anemia in 30% of cases, neutropenia in 24%, and 2 probable cases of mitomycin-induced pneumonitis. The objective response rate was 38% (17 of 45 were partial responses), and the median response duration was 12 months. The median survival time was 16 months. There were no differences in response or survival between the 31 patients treated with growth factors and the 14 patients treated without them. Survival was slightly better for responders than for nonresponders who had stable disease or progression (20 vs. 10 months, P < 0.05).
This four-drug combination was effective, with a notably high response rate, acceptable toxicity, and good adherence to protocol doses. The impact on survival was limited.
恶性胸膜间皮瘤因其对治疗具有抗性,预后较差。作者开展了一项II期试验,在癌症与白血病B组顺铂-丝裂霉素方案中加入两种药物(依托泊苷和5-氟尿嘧啶),以确定更有效的化疗方案。
45例确诊为II期恶性胸膜间皮瘤的患者前瞻性纳入本研究。31例患者在第1天接受顺铂60mg/m²,第1 - 4天接受5-氟尿嘧啶600mg,第1 - 4天接受亚叶酸100mg/m²,第3天接受丝裂霉素C 10mg/m²,第1 - 3天接受依托泊苷100mg/m²静脉注射,并给予预防性造血生长因子。14例患者接受顺铂、5-氟尿嘧啶、亚叶酸和丝裂霉素C,方案不变,第1 - 21天口服依托泊苷50mg,不使用生长因子(每28天1个周期)。组织学类型包括上皮型(33例)、肉瘤型(6例)、混合型(3例)和未明确类型(3例)。
共进行了211个周期的治疗。治疗耐受性良好,主要毒性为血液学毒性:30%的病例出现贫血,24%出现中性粒细胞减少,2例可能为丝裂霉素诱发的肺炎。客观缓解率为38%(45例中有17例部分缓解),中位缓解持续时间为12个月。中位生存时间为16个月。接受生长因子治疗的31例患者与未接受生长因子治疗的14例患者在缓解或生存方面无差异。缓解者的生存略优于病情稳定或进展的未缓解者(20个月对10个月,P < 0.05)。
这种四联药物组合有效,缓解率显著较高,毒性可接受,且对方案剂量的依从性良好。对生存的影响有限。