Kuse R, Heilmann H P, Calavrezos A, Hausmann K
Dtsch Med Wochenschr. 1983 Dec 23;108(51-52):1948-54. doi: 10.1055/s-2008-1069855.
Based on repeated interval analyses, radiotherapy and cytostatic drug therapy were stepwise intensified and combined in 264 patients diagnosed between 1976 and 1981 as having histopathologically low-malignant centroblastic-centrocytic (cb/cc; n = 106), centrocytic (cc; n = 34) or immunocytic lymphoma (n = 124). The number of treatment failures and recurrences were clearly reduced. There were three prognostic steps in survival probability: 90% after seven years for stages IA-IVA of the cb/cc lymphoma as well as for the extranodal lymphoplasmocytoid and lymphoplasmocytic immunocytomas, stages I-IV of Ann Arbor, and stages 0-II of the Rai classifications. In the Rai stages III and IV these immunocytomas had a definitely worse prognosis, at 60%. Prognostically most unfavourable, at levels of around or below 30%, were the B forms of cb/cc lymphomas, all stages of centrocytoma and the polymorph-cell immunocytomas. The survival rate of the cb/cc lymphomas was increased by about 33%, compared with cases of Brill-Symmers' disease between 1970 and 1975. The alternating use of cytostatic combinations seems to be more favourable among the previously little affected centrocytomas and the polymorph-cell immunocytomas.
基于重复区间分析,对1976年至1981年间诊断为组织病理学低恶性中心母细胞-中心细胞型(cb/cc;n = 106)、中心细胞型(cc;n = 34)或免疫细胞淋巴瘤(n = 124)的264例患者,逐步加强放疗和细胞抑制药物治疗并联合应用。治疗失败和复发的数量明显减少。生存概率有三个预后阶段:cb/cc淋巴瘤的IA-IVA期以及结外淋巴浆细胞样和淋巴浆细胞性免疫细胞瘤、Ann Arbor分期的I-IV期、Rai分类的0-II期,七年后生存率为90%。在Rai分期III和IV期,这些免疫细胞瘤的预后明显较差,为60%。预后最不利的是cb/cc淋巴瘤的B型、中心细胞瘤的所有阶段以及多形细胞免疫细胞瘤,生存率在30%左右或以下。与1970年至1975年间的布-西病病例相比,cb/cc淋巴瘤的生存率提高了约33%。在先前受影响较小的中心细胞瘤和多形细胞免疫细胞瘤中,交替使用细胞抑制联合方案似乎更为有利。