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两种惰性淋巴瘤实体的临床分析:套细胞淋巴瘤和边缘区淋巴瘤(包括黏膜相关淋巴组织和单核细胞样B细胞亚类):西南肿瘤协作组研究

A clinical analysis of two indolent lymphoma entities: mantle cell lymphoma and marginal zone lymphoma (including the mucosa-associated lymphoid tissue and monocytoid B-cell subcategories): a Southwest Oncology Group study.

作者信息

Fisher R I, Dahlberg S, Nathwani B N, Banks P M, Miller T P, Grogan T M

机构信息

Loyola University Stritch School of Medicine, Maywood, IL.

出版信息

Blood. 1995 Feb 15;85(4):1075-82.

PMID:7849295
Abstract

The objectives of this study were (1) to determine the clinical presentation and natural history associated with two newly recognized pathologic entities termed mantle cell lymphoma (MCL) and marginal zone lymphoma (MZL), including the mucosa-associated lymphoid tissue (MALT) and monocytoid B-cell subcategories, and (2) to determine whether these entities differ clinically from the other relatively indolent non-Hodgkin's lymphomas with which they have been previously classified. We reviewed the conventional pathology and clinical course of 376 patients who had no prior therapy; had stage III/IV disease; were classified as Working Formulation categories A, B, C, D, or E; and received cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) on Southwest Oncology Group (SWOG) studies no. 7204, 7426, or 7713. All slides were reviewed by the three pathologists who reached a consensus diagnosis. Age, sex, performance status, bone marrow and/or gastrointestinal involvement, failure-free survival, and overall survival were compared among all the categories. We found that (1) MCL and MZL each represent approximately 10% of stage III or IV patients previously classified as Working Formulation categories A through E and treated with CHOP on SWOG clinical trials; (2) the failure-free survival and overall survival of patients with MZL is the same as that of patients with Working Formulation categories A through E, but the failure-free survival and overall survival of the monocytoid B-cell patients were higher than that of the MALT lymphoma patients (P = .009 and .007, respectively); and (3) the failure-free survival and overall survival of patients with MCL is significantly worse than that of patients with Working Formulation categories A through E (P = .0002 and .0001, respectively). In conclusion, patients with advanced stage MALT lymphomas may have a more aggressive course than previously recognized. Patients with MCL do not have an indolent lymphoma and are candidates for innovative therapy.

摘要

本研究的目的是

(1)确定与两种新确认的病理实体相关的临床表现和自然病史,这两种病理实体分别称为套细胞淋巴瘤(MCL)和边缘区淋巴瘤(MZL),包括黏膜相关淋巴组织(MALT)和单核细胞样B细胞亚类;(2)确定这些实体在临床上是否与之前归为同一类的其他相对惰性的非霍奇金淋巴瘤不同。我们回顾了376例未接受过先前治疗、患有III/IV期疾病、被归类为工作分类法中的A、B、C、D或E类且在西南肿瘤协作组(SWOG)的第7204、7426或7713号研究中接受环磷酰胺、阿霉素、长春新碱、泼尼松(CHOP)方案治疗的患者的传统病理和临床病程。所有玻片均由三位病理学家复查,他们达成了共识诊断。比较了所有类别患者的年龄、性别、体能状态、骨髓和/或胃肠道受累情况、无进展生存期和总生存期。我们发现:(1)MCL和MZL在先前被归类为工作分类法中A至E类并在SWOG临床试验中接受CHOP治疗的III期或IV期患者中各占约10%;(2)MZL患者的无进展生存期和总生存期与工作分类法中A至E类患者相同,但单核细胞样B细胞患者的无进展生存期和总生存期高于MALT淋巴瘤患者(P值分别为0.009和0.007);(3)MCL患者的无进展生存期和总生存期明显差于工作分类法中A至E类患者(P值分别为0.0002和0.0001)。总之,晚期MALT淋巴瘤患者的病程可能比之前认为的更具侵袭性。MCL患者并非患有惰性淋巴瘤,而是创新疗法的候选对象。

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