Pichert G, Peters J, Stahel R A, Dommann C, Joss R, Gebbers J O, Kroner T, Sulser H, Honegger H P, Maurer R
University Hospital Zürich, Switzerland.
Ann Oncol. 1992 Sep;3(8):645-9. doi: 10.1093/oxfordjournals.annonc.a058295.
Eighty-three previously untreated patients with aggressive non-Hodgkin's lymphomas were treated with either MACOP-B (23 patients) or VACOP-B (60 patients) as originally described by Klimo and Conners [1, 2]. Their median age was 46 years. Thirty-seven patients had stage I or II and 46 stage III or IV disease. The tumor histopathology was reviewed in all cases. Sixty-five patients had intermediate grade and 18 high-grade non-Hodgkin's lymphomas according to the International Working Formulation. The rate of complete response was 74% for MACOP-B and 76% for VACOP-B. At the time of analysis the duration of follow-up was 50 months for the MACOP-B and 22 months for the VACOP-B group. The actuarial three-year progression-free survival was 35 +/- 10% for the MACOP-B group, 48 +/- 11% for the VACOP-B group, and 46 +/- 7% for all patients. Treatment mortality was 6%. A univariate and a multivariate analysis of selected pretreatment parameters and of regimen demonstrated that stage III or IV, high-grade lymphoma, and elevated serum LDH, but not the type of regimen, are significantly associated with poor progression-free survival in our patient population.
83例既往未接受过治疗的侵袭性非霍奇金淋巴瘤患者,按照Klimo和Conners最初描述的方法[1,2],分别接受MACOP-B方案(23例患者)或VACOP-B方案(60例患者)治疗。他们的中位年龄为46岁。37例患者为Ⅰ期或Ⅱ期,46例为Ⅲ期或Ⅳ期疾病。所有病例均对肿瘤组织病理学进行了复查。根据国际工作分类法,65例患者为中度恶性,18例为高度恶性非霍奇金淋巴瘤。MACOP-B方案的完全缓解率为74%,VACOP-B方案为76%。在分析时,MACOP-B组的随访时间为50个月,VACOP-B组为22个月。MACOP-B组的3年无进展生存精算率为35±10%,VACOP-B组为48±11%,所有患者为46±7%。治疗死亡率为6%。对选定的预处理参数和治疗方案进行单因素和多因素分析表明,Ⅲ期或Ⅳ期、高度恶性淋巴瘤以及血清乳酸脱氢酶升高,但治疗方案类型并非如此,与我们患者群体中较差的无进展生存显著相关。