Longo D L, DeVita V T, Duffey P L, Wesley M N, Ihde D C, Hubbard S M, Gilliom M, Jaffe E S, Cossman J, Fisher R I
Division of Cancer Treatment, National Cancer Institute, Bethesda, MD.
J Clin Oncol. 1991 Jan;9(1):25-38. doi: 10.1200/JCO.1991.9.1.25.
One hundred ninety-three patients with stage II, III, or IV follicular large-cell, diffuse large-cell, diffuse mixed, immunoblastic, or diffuse small noncleaved-cell (non-Burkitt's) lymphoma were randomized to receive either cyclophosphamide 650 mg/m2 intravenously (IV), doxorubicin 25 mg/m2 IV, etoposide 120 mg/m2 IV on day 1, mechlorethamine 6 mg/m2 IV, vincristine 1.4 mg/m2 (no cap at 2 mg total dose) IV on day 8, prednisone 60 mg/m2 orally daily days 1 through 14, procarbazine 100 mg/m2 orally daily days 8 through 14, and methotrexate 500 mg/m2 IV on day 15 with leucovorin 50 mg/m2 orally every 6 hours for four doses beginning 24 hours after methotrexate with cycles repeated every 28 days (ProMACE-MOPP) or same day-1 treatment as ProMACE-MOPP plus cytarabine 300 mg/m2 IV, bleomycin 5 U/m2 IV, vincristine 1.4 mg/m2 (no cap at 2 mg total dose) IV, and methotrexate 120 mg/m2 IV on day 8, leucovorin 25 mg/m2 orally every 6 hours for four doses beginning 24 hours after methotrexate, and prednisone 60 mg/m2 orally daily days 1 through 14 with cycles repeated every 21 days (ProMACE-CytaBOM). Co-trimoxazole two double-strength tablets orally twice daily throughout the period of treatment was added to the ProMACE-CytaBOM regimen when an increased risk of Pneumocystis carinii pneumonia was found in the first 35 patients receiving this combination. Median follow-up is 5 years. Among the 99 patients treated with ProMACE-MOPP, 73 achieved a complete remission (CR) (74%), 30 complete responders have relapsed (41%), and 45 patients have died (45%), including two (2%) of treatment-related causes. Among the 94 patients treated with ProMACE-CytaBOM, 81 achieved a CR (86%), 22 complete responders have relapsed (27%), and 31 patients have died (33%). The complete response rate (P2 = .048) and survival (P2 = .046) were significantly higher for patients treated with ProMACE-CytaBOM. The mortality of ProMACE-CytaBOM treatment overall was six of 94 patients (6.4%). There was no treatment-related mortality among patients treated with prophylactic co-trimoxazole (n = 59). ProMACE-CytaBOM combination chemotherapy with co-trimoxazole prophylaxis is a safe and effective treatment for patients with aggressive histology malignant lymphoma and is superior to ProMACE-MOPP.
193例II期、III期或IV期滤泡大细胞、弥漫大细胞、弥漫混合、免疫母细胞或弥漫小无裂细胞(非伯基特氏)淋巴瘤患者被随机分组,分别接受以下治疗方案:环磷酰胺650mg/m²静脉注射(IV)、阿霉素25mg/m²静脉注射、依托泊苷120mg/m²静脉注射,于第1天给药;氮芥6mg/m²静脉注射、长春新碱1.4mg/m²(总剂量不超过2mg)静脉注射,于第8天给药;泼尼松60mg/m²口服,每日1次,第1天至第14天给药;丙卡巴肼100mg/m²口服,每日1次,第8天至第14天给药;甲氨蝶呤500mg/m²静脉注射,于第15天给药,亚叶酸钙50mg/m²口服,每6小时1次,共4剂,于甲氨蝶呤给药24小时后开始,每28天重复1个周期(ProMACE-MOPP方案);或者与ProMACE-MOPP方案第1天治疗相同,加用阿糖胞苷300mg/m²静脉注射、博来霉素5U/m²静脉注射、长春新碱1.4mg/m²(总剂量不超过2mg)静脉注射、甲氨蝶呤120mg/m²静脉注射,于第8天给药,亚叶酸钙25mg/m²口服,每6小时1次,共4剂,于甲氨蝶呤给药24小时后开始,泼尼松60mg/m²口服,每日1次,第1天至第14天给药,每21天重复1个周期(ProMACE-CytaBOM方案)。当发现接受该联合治疗的前35例患者卡氏肺孢子虫肺炎风险增加时,在ProMACE-CytaBOM方案中整个治疗期间加用复方新诺明两片双倍剂量片剂口服,每日2次。中位随访时间为5年。在接受ProMACE-MOPP方案治疗的99例患者中,73例达到完全缓解(CR)(74%),30例完全缓解者复发(41%),45例患者死亡(45%),其中2例(2%)死于治疗相关原因。在接受ProMACE-CytaBOM方案治疗的94例患者中,81例达到CR(86%),22例完全缓解者复发(27%),31例患者死亡(33%)。接受ProMACE-CytaBOM方案治疗的患者完全缓解率(P2 = 0.048)和生存率(P2 = 0.046)显著更高。ProMACE-CytaBOM方案治疗的总体死亡率为94例患者中的6例(6.4%)。接受预防性复方新诺明治疗的患者(n = 59)中无治疗相关死亡。ProMACE-CytaBOM联合化疗加复方新诺明预防对侵袭性组织学类型恶性淋巴瘤患者是一种安全有效的治疗方法,且优于ProMACE-MOPP方案。