Diviné M, Lepage E, Brière J, Pautier P, Dupriez B, Lederlin P, Mineur P, Tilly H, Blanc M, Audhuy B, Herbrecht R, Coiffier B, Reyes F
Hôpital Henri Mondor, Créteil, France.
J Clin Oncol. 1996 Jan;14(1):240-8. doi: 10.1200/JCO.1996.14.1.240.
To study the prognostic significance of the small non-cleaved-cell lymphoma (SNCCL) histologic subtype, we compared the outcome of adult patients with SNCCL with that of patients with aggressive lymphoma other than SNCCL by means of two case-controlled studies.
We analyzed the results of the doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone (ACVBP) regimen used as a reference scheme in our cooperative study group (Groupe d'Etude des Lymphomes de l'Adult [GELA]) in 52 adult SNCCL patients with no bone marrow (BM) or CNS involvement. Forty-five SNCCL patients younger than 60 years could be compared with two separate case-matched groups of patients with aggressive lymphoma other than SNCCL undergoing the same therapeutic regimen. In the first case-controlled study, matching ensured identity of each risk factor of the age-adjusted International Index (ie, Ann Arbor stage, performance status, and lactate dehydrogenase [LDH] level); in the second study, matching was performed according to the number of presenting risk factors (zero, one, two, or three), regardless of their nature.
The 5-year overall survival rates were not significantly different between SNCCL and control patients in both case-controlled studies: 48% versus 51% in the first study, and 48% versus 55% in the second study.
These results support the thesis that in patients with no bone marrow or CNS involvement, the SNCCL histologic subtype does not confer a prognosis worse than that of other aggressive lymphoma.
为研究小无裂细胞淋巴瘤(SNCCL)组织学亚型的预后意义,我们通过两项病例对照研究,比较了成年SNCCL患者与非SNCCL侵袭性淋巴瘤患者的预后情况。
我们分析了在我们的合作研究组(成人淋巴瘤研究组[GELA])中,将阿霉素、环磷酰胺、长春地辛、博来霉素和泼尼松(ACVBP)方案用作参考方案,对52例无骨髓(BM)或中枢神经系统(CNS)受累的成年SNCCL患者的治疗结果。45例年龄小于60岁的SNCCL患者可与两组分别与之病例匹配的、接受相同治疗方案的非SNCCL侵袭性淋巴瘤患者进行比较。在第一项病例对照研究中,匹配确保了年龄校正国际指数的每个风险因素(即Ann Arbor分期、体能状态和乳酸脱氢酶[LDH]水平)相同;在第二项研究中,根据存在的风险因素数量(零个、一个、两个或三个)进行匹配,而不考虑其性质。
在两项病例对照研究中,SNCCL患者与对照患者的5年总生存率均无显著差异:第一项研究中分别为48%和51%,第二项研究中分别为48%和55%。
这些结果支持以下论点,即在无骨髓或中枢神经系统受累的患者中,SNCCL组织学亚型的预后并不比其他侵袭性淋巴瘤差。