Comella P, Scoppa G, Abate G, Comella G, Apice G, Castello G, Pergola M, Giordano G G, Coucourde F, Zarrilli D
Tumori. 1982 Apr 30;68(2):137-42. doi: 10.1177/030089168206800207.
From January 1978 to December 1980, 42 patients with early stage non-Hodgkin's lymphoma other than of the gastrointestinal tract were treated with radiotherapy and combination chemotherapy. Eighteen patients in stage I were submitted to locally extended-field radiotherapy up to a mean dose of 48 Gy with a Co60 source and, after a 3-week rest period, to 6 cycles of combination chemotherapy. Twenty-four patients in stage II received 3 cycles of combination chemotherapy before and after irradiation, the same as for stage I. Combination chemotherapy consisted of cyclophosphamide, vincristine and prednisone (CVP) for 15 cases with favorable histology (3 NWDL, 1 NPDI, 11 DWDL), whereas it included cyclophosphamide, adriamycin, vincristine and prednisone (CHOP) for 27 cases with unfavorable histology (20 DPDL, 3 DM, 4 DH). Complete remission (CR) was achieved in 35/42 (83%) patients, with a highly significant difference between stage I (100%) and stage II (71%). After 42 months of follow-up, the probability of survival for all patients was 72%. Survival was better for stage I (88%) than for stage II (68%) and for favorable histology (87%) as compared to unfavorable histology (70%). Furthermore, survival was highly influenced by response to therapy. Indeed, actuarial survival rate for CR was 91% as compared to a median survival time of 10.2 months for the remaining patients. Four patients, all with poor histology, relapsed after 5-24 (mean 11) months of CR. Only one of them had an extension in extranodal sites and eventually died, despite the salvage treatment utilized. In our experience, locally extended-field irradiation combined with chemotherapy gave a high proportion of CR and seemed to prevent relapses, particularly in extranodal site.
1978年1月至1980年12月,42例非胃肠道早期非霍奇金淋巴瘤患者接受了放疗和联合化疗。18例I期患者接受局部扩大野放疗,使用钴60源,平均剂量达48 Gy,休息3周后,进行6周期联合化疗。24例II期患者在放疗前后各接受3周期联合化疗,与I期相同。联合化疗中,15例组织学类型良好(3例结节性淋巴细胞为主型、1例富于T细胞/组织细胞型、11例弥漫性大B细胞淋巴瘤)的患者采用环磷酰胺、长春新碱和泼尼松(CVP)方案,而27例组织学类型不良(20例弥漫性大B细胞淋巴瘤、3例间变性大细胞淋巴瘤、4例富于T细胞/组织细胞型)的患者采用环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)方案。42例患者中有35例(83%)达到完全缓解(CR),I期(100%)和II期(71%)之间存在高度显著差异。随访42个月后,所有患者的生存率为72%。I期患者(88%)的生存率高于II期患者(68%),组织学类型良好患者(87%)的生存率高于组织学类型不良患者(70%)。此外,生存情况受治疗反应的影响很大。实际上,CR患者的精算生存率为91%,而其余患者的中位生存时间为10.2个月。4例患者组织学类型均较差,在CR 5 - 24个月(平均11个月)后复发。其中只有1例出现结外部位扩展,尽管采用了挽救治疗,最终仍死亡。根据我们的经验,局部扩大野照射联合化疗能使CR比例很高,且似乎能预防复发,尤其是在结外部位。