Callea V, Clò V, Morabito F, Baldini L, Stelitano C, Narni F, Avanzini P, Brugiatelli M, Silingardi V
Dipartimento di Emato-Oncologia, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy.
Haematologica. 1998 Nov;83(11):993-7.
Mantle cell lymphoma is a recently recognized histologic entity with specific biological and clinical features. Clinically, the reported unfavorable outcome of these patients has focused attention on this category of non-Hodgkin's lymphoma (NHL).
The slide specimens of 69 NHL patients, originally classified as Working Formulation (WF) group B and E, were reviewed. The clinical features at presentation, response to therapy, response duration and survival were analyzed in cases reclassified as MCL. The correlation between clinical and histologic characteristics and the final outcome was evaluated.
Out of 69 cases, 34 specimens were reclassified as MCL; in 6 patients, previously classified as WF group B, the nodular pattern was confirmed; in 2 instances the blastoid form was recognized. After a median follow-up of 35.7 months, the entire series displayed a median overall survival of 41.2 months; a significantly longer survival was associated with the nodular histologic pattern, IPI score < 2, response achievement, and a higher Hb level. The vast majority of patients received anthracycline-containing combination chemotherapy. Complete remission rate was 38.8% and overall response rate was 67.6%; response achievement was significantly influenced only by Hb level. Median response duration was 23.3 months.
The present study confirms the unfavorable clinical course of MCL and the possible need for an alternative therapeutic strategy for this NHL category. Therefore, the correct identification of MCL at diagnosis appears of relevance.
套细胞淋巴瘤是一种最近才被认识的具有特定生物学和临床特征的组织学实体。临床上,这些患者报告的不良预后已使人们将注意力集中在这类非霍奇金淋巴瘤(NHL)上。
回顾了69例最初分类为工作分类法(WF)的B组和E组的NHL患者的玻片标本。对重新分类为MCL的病例分析了其就诊时的临床特征、对治疗的反应、反应持续时间和生存期。评估了临床和组织学特征与最终结果之间的相关性。
69例病例中,34份标本重新分类为MCL;6例先前分类为WF的B组患者,结节型得到确认;2例识别出母细胞样形态。中位随访35.7个月后,整个系列的中位总生存期为41.2个月;结节组织学类型、国际预后指数(IPI)评分<2、达到反应以及较高的血红蛋白(Hb)水平与显著更长的生存期相关。绝大多数患者接受了含蒽环类药物的联合化疗。完全缓解率为38.8%,总缓解率为67.6%;仅Hb水平对达到反应有显著影响。中位反应持续时间为23.3个月。
本研究证实了MCL的不良临床病程以及可能需要针对这类NHL采取替代治疗策略。因此,诊断时正确识别MCL似乎具有重要意义。