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对北美人类 T 细胞嗜淋巴细胞病毒 1 相关性成人 T 细胞白血病/淋巴瘤患者预后因素的批判性分析:一项多中心临床病理经验和新的预后评分。

A critical analysis of prognostic factors in North American patients with human T-cell lymphotropic virus type-1-associated adult T-cell leukemia/lymphoma: a multicenter clinicopathologic experience and new prognostic score.

机构信息

Division of Medical Oncology, Department of Medicine, Columbia University College of Physicians and Surgeons, Milstein Hospital Building, New York, New York 10032, USA.

出版信息

Cancer. 2010 Jul 15;116(14):3438-46. doi: 10.1002/cncr.25147.

DOI:10.1002/cncr.25147
PMID:20564100
Abstract

BACKGROUND

To define the clinicopathologic and prognostic features of patients with human T-cell lymphotropic virus type-1 (HTLV-1)-associated adult T-cell leukemia/lymphoma (ATLL) in North America, standard criteria were used to identify patients with ATLL.

METHODS

Statistical analyses used included descriptive statistics, Kaplan-Meir survival analysis, and recursive partitioning.

RESULTS

Eighty-nine patients were identified between August 1992 and May 2007, including 37 (41.6%) males and 52 (58.4%) females with a median age of 50 years (range, 22-82 years). All but 6 patients had immigrated to the United States from the Caribbean, Latin America, or Africa. The acute subtype predominated (68.5%). The majority of patients received a combination-alkylator-based chemotherapy regimen in the front-line setting (72.6%). The most common regimen was cyclophosphamide, doxorubicin, vincristine, and prednisone at standard doses or attenuated and/or with methotrexate (CHOP-like), which produced an overall response rate of 64.1%. Despite initial responses to therapy, the median overall survival for all subtypes was 24 weeks (range, 0.9-315 weeks). Although the International Prognostic Index and Prognostic Index for peripheral T-cell lymphoma unspecified identified subsets of patients, these models were not completely predictive. A recursive partitioning analysis was performed on the data, which successfully identified 3 prognostic categories based on Eastern Cooperative Oncology Group performance status, stage, age, and calcium level at diagnosis.

CONCLUSIONS

This series proposed a new prognostic model for patients with HTLV-1-associated ATLL and confirmed a poor outcome for these patients in North America.

摘要

背景

为了定义北美人种 T 细胞嗜淋巴细胞病毒 1 型(HTLV-1)相关成人 T 细胞白血病/淋巴瘤(ATLL)患者的临床病理和预后特征,使用标准标准来识别 ATLL 患者。

方法

使用的统计分析包括描述性统计、Kaplan-Meier 生存分析和递归分区。

结果

1992 年 8 月至 2007 年 5 月期间共确定了 89 例患者,其中男性 37 例(41.6%),女性 52 例(58.4%),中位年龄为 50 岁(范围,22-82 岁)。除 6 例患者外,所有患者均从加勒比海、拉丁美洲或非洲移民到美国。急性亚型为主(68.5%)。大多数患者在前一线接受了联合烷化剂为基础的化疗方案(72.6%)。最常见的方案是标准剂量或减毒的环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP 样),总缓解率为 64.1%。尽管对治疗有初步反应,但所有亚型的中位总生存期均为 24 周(范围,0.9-315 周)。尽管国际预后指数和未特指外周 T 细胞淋巴瘤的预后指数确定了患者的亚组,但这些模型并不完全具有预测性。对数据进行了递归分区分析,成功地根据东部合作肿瘤学组的表现状态、分期、年龄和诊断时的钙水平确定了 3 个预后类别。

结论

本系列提出了一种新的 HTLV-1 相关 ATLL 患者的预后模型,并证实了北美患者的预后不良。

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