A prognostic score for AIDS-related diffuse large B-cell lymphoma in Brazil

被引:8
作者
Tanaka, Paula Yurie [1 ]
Pracchia, Luis Fernando [2 ]
Bellesso, Marcelo [2 ]
Fischer Chamone, Dalton Alencar [2 ]
Calore, Edenilson Eduardo [3 ]
Pereira, Juliana [2 ]
机构
[1] Inst Infectol Emilio Ribas, Hematol Sect, BR-01246900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Hematol, Hosp Clin, Sao Paulo, Brazil
[3] Inst Infectol Emilio Ribas, Pathol Sect, BR-01246900 Sao Paulo, Brazil
关键词
Lymphoma; HIV; AIDS; NON-HODGKINS-LYMPHOMA; VIRUS-RELATED LYMPHOMA; INTENSIVE CHEMOTHERAPY; CHOP; RITUXIMAB; SURVIVAL; CYCLOPHOSPHAMIDE; DOXORUBICIN; ETOPOSIDE; TRIAL;
D O I
10.1007/s00277-009-0761-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to evaluate a prognostic score for aids-related lymphoma (ARL). A retrospective study of 104 patients with ARL treated between January 1999 and December 2007 was conducted. Diffuse large B-cell lymphoma (DLBC) was the most observed histological type (79.8%). The median CD4 lymphocyte count at lymphoma diagnosis was 125 cells per microliter. Treatment response could be evaluated in 83 (79.8%) patients, and 38 (45.8%) reached complete remission (CR); overall response rate was 51.8% (95 CI = 38.5-65.1%). After a median follow-up of 48 months, the 4-year overall survival (OS) rate among all patients was 35.8%, with a median survival time of 9.7 months (95% CI = 5.5-13.9 months). The survival risk factors observed in multivariate analysis (previous AIDS and high-intermediate/high international prognostic index (IPI)) were combined to construct a risk score, which divided the whole patient population in three distinct groups as low, intermediate, and high risk. When this score was applied to DLBC patients, a clear distinction in response rates and in OS could be demonstrated. Median disease-free survival (DFS) for patients that achieved CR was not reached, and DFS in 4 years was 83.0%. Our results show that the reduced OS observed could be explained by poor immune status with advanced stage of disease seen in our population of HIV-positive patients. Further studies will be needed to clarify the role of different treatment approaches for ARL in the setting of marked immunosuppression and to identify a group of patients to whom intensive therapy could be performed with a curative intent.
引用
收藏
页码:45 / 51
页数:7
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