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小无裂细胞淋巴瘤组织学亚型在成年患者中是否为不良预后因素?一项病例对照分析。成人淋巴瘤研究组。

Is the small non-cleaved-cell lymphoma histologic subtype a poor prognostic factor in adult patients? A case-controlled analysis. The Groupe d'Etude des Lymphomes de l'Adulte.

作者信息

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

机构信息

Hôpital Henri Mondor, Créteil, France.

出版信息

J Clin Oncol. 1996 Jan;14(1):240-8. doi: 10.1200/JCO.1996.14.1.240.

Abstract

PURPOSE

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

患者与方法

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。

结果

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%。

结论

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。

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