Fisher R I, Longo D L, DeVita V T, Hubbard S M, Miller T P, Young R C
National Cancer Institute, Bethesda, Maryland.
Ann Oncol. 1991 Jan;2 Suppl 1:33-5. doi: 10.1093/annonc/2.suppl_1.33.
Initial results from studies with third-generation combination chemotherapy regimens for the treatment of aggressive non-Hodgkin's lymphomas (NHL) demonstrated complete remission (CR) rates higher than those reported with first-generation regimens. Long-term follow-up of these studies is required to know if the increased number of CRs translates into an increased number of long-term disease-free survivors. In this report, results obtained with one of the third-generation regimens, ProMACE (prednisone/methotrexate/doxorubicin/cyclophosphamide/etoposide)-Cyta BOM (cytarabine/bleomycin/vincristine/methotrexate) are described. From 1981 to 1988, 193 patients with stage II, III, or IV aggressive NHL treated at the National Cancer Institute were randomly assigned to receive either ProMACE (day 1)-CytaBOM (day 8) or ProMACE (day 1)-MOPP (mechlorethamine/vincristine/procarbazine/prednisone) (day 8). With a median follow-up of 5 years, the CR rate was 86% for ProMACE-CytaBOM v 74% for ProMACE-MOPP (P = 0.048). A plateau in the disease-free survival curve is seen at 69% for ProMACE-CytaBOM v 54% for ProMACE-MOPP (P = 0.082). A plateau is also seen in the overall survival curves at 69% for ProMACE-CytaBOM v 53% for ProMACE-MOPP (P = 0.046). The Southwest Oncology Group also conducted a phase II study of ProMACE-CytaBOM in 78 patients with stages II to IV intermediate- or high-grade NHL to determine the CR rate and long-term disease-free survival of this regimen in a national cooperative group setting. The CR rate was 65%. With a median follow-up of 38 months, disease-free survival is 50% at 3 years and overall survival is 57% at the same time point.(ABSTRACT TRUNCATED AT 250 WORDS)
采用第三代联合化疗方案治疗侵袭性非霍奇金淋巴瘤(NHL)的研究初步结果显示,其完全缓解(CR)率高于第一代方案。需要对这些研究进行长期随访,以了解CR数量的增加是否会转化为长期无病生存者数量的增加。在本报告中,描述了第三代方案之一ProMACE(泼尼松/甲氨蝶呤/阿霉素/环磷酰胺/依托泊苷)-Cyta BOM(阿糖胞苷/博来霉素/长春新碱/甲氨蝶呤)的研究结果。1981年至1988年,美国国立癌症研究所治疗的193例II、III或IV期侵袭性NHL患者被随机分配接受ProMACE(第1天)-CytaBOM(第8天)或ProMACE(第1天)-MOPP(氮芥/长春新碱/丙卡巴肼/泼尼松)(第8天)治疗。中位随访5年,ProMACE-CytaBOM的CR率为86%,而ProMACE-MOPP为74%(P = 0.048)。ProMACE-CytaBOM的无病生存曲线在69%处出现平台期,而ProMACE-MOPP为54%(P = 0.082)。总生存曲线在ProMACE-CytaBOM为69%处也出现平台期,而ProMACE-MOPP为53%(P = 0.046)。西南肿瘤协作组也对7�例II至IV期中级或高级NHL患者进行了ProMACE-CytaBOM的II期研究,以确定该方案在全国协作组环境中的CR率和长期无病生存情况。CR率为65%。中位随访38个月,3年时无病生存率为50%,同一时间点总生存率为57%。(摘要截选至250字)