Gill P S, Rarick M, McCutchan J A, Slater L, Parker B, Muchmore E, Bernstein-Singer M, Akil B, Espina B M, Krailo M
Department of Internal Medicine, University of Southern California, School of Medicine, Los Angeles.
Am J Med. 1991 Apr;90(4):427-33.
Patients with acquired immunodeficiency syndrome (AIDS)-related epidemic Kaposi's sarcoma generally respond well to cytotoxic chemotherapy. However, due to the associated myelosuppression, these patients are at risk for developing complicating infections that may affect survival. We therefore conducted a multi-center randomized clinical trial comparing single-agent against combination chemotherapy in advanced AIDS-related Kaposi's sarcoma. Low-dose chemotherapy was employed to evaluate its role in combination therapy for this disease and the toxicities associated with the lower intensity.
Sixty-one patients with extensive mucocutaneous Kaposi's sarcoma or visceral involvement were randomized for treatment with low-dose Adriamycin (doxorubicin, 20 mg/m2) alone (31 cases) or in combination with bleomycin and vincristine (ABV) (30 cases). Patients were randomized within strata based on prognostic features associated with shorter survival in prior studies. Both treatment arms were evenly matched at study entry.
Complete and partial tumor remissions were significantly higher with ABV (88%) than with Adriamycin alone (48%) (p = 0.004). The median survival was 9 months in both groups. Study entry criteria significantly associated with shorter survival included CD4 lymphocyte counts less than 100/mm3, hemoglobin level less than 10 g/dL, a history of constitutional symptoms, and a prior history of opportunistic infection(s). Toxicities were similar in both arms, and the regimens were well tolerated. Neutropenia (granulocyte count less than 1,000/mm3) occurred in 34% of patients receiving Adriamycin alone and in 52% of patients receiving ABV and was progressive in successive courses of chemotherapy in both treatment arms. The development of AIDS-defined opportunistic infections was relatively infrequent during therapy (14%).
Low-dose ABV is an effective chemotherapy regimen for the treatment of extensive Kaposi's sarcoma. ABV chemotherapy is associated with significantly higher responses than Adriamycin alone and with acceptable toxicity.
获得性免疫缺陷综合征(AIDS)相关的流行性卡波西肉瘤患者通常对细胞毒性化疗反应良好。然而,由于相关的骨髓抑制,这些患者有发生可能影响生存的并发感染的风险。因此,我们开展了一项多中心随机临床试验,比较晚期AIDS相关卡波西肉瘤的单药化疗与联合化疗。采用低剂量化疗来评估其在该疾病联合治疗中的作用以及与较低强度相关的毒性。
61例有广泛黏膜皮肤卡波西肉瘤或内脏受累的患者被随机分组,分别接受低剂量阿霉素(多柔比星,20mg/m²)单药治疗(31例)或与博来霉素和长春新碱联合治疗(ABV方案,30例)。根据先前研究中与较短生存期相关的预后特征,患者在各层内随机分组。两个治疗组在研究入组时均衡匹配。
ABV方案(88%)的完全和部分肿瘤缓解率显著高于阿霉素单药治疗组(48%)(p = 0.004)。两组的中位生存期均为9个月。与较短生存期显著相关的研究入组标准包括CD4淋巴细胞计数低于100/mm³、血红蛋白水平低于10g/dL、有全身症状史以及有机会性感染史。两组的毒性相似,且方案耐受性良好。接受阿霉素单药治疗的患者中有34%发生中性粒细胞减少(粒细胞计数低于1000/mm³),接受ABV方案治疗的患者中有52%发生中性粒细胞减少,且在两个治疗组的连续化疗疗程中均呈进行性。治疗期间,AIDS定义的机会性感染的发生相对较少(14%)。
低剂量ABV是治疗广泛卡波西肉瘤的有效化疗方案。ABV化疗的反应显著高于阿霉素单药治疗,且毒性可接受。