Risk assessment in human immunodeficiency virus-associated acute myeloid leukemia

被引:9
作者
Evans, Michael W. [1 ]
Sung, Anthony D. [2 ]
Gojo, Ivana [1 ]
Tidwell, Michael [1 ]
Greer, Jacqueline [2 ]
Levis, Mark [2 ]
Karp, Judith [2 ]
Baer, Maria R. [1 ]
机构
[1] Univ Maryland, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Johns Hopkins Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
Human immunodeficiency virus; acquired immunodeficiency syndrome; acute myeloid leukemia; risk assessment; ACUTE MYELOBLASTIC-LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; CYTOGENETIC ABNORMALITIES; HIV; THERAPY; CANCER; CHEMOTHERAPY; PATIENT; AML;
D O I
10.3109/10428194.2011.624228
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD4 count <= 200 X 10(6) cells/L has been identified as a predictor of short survival in HIV-associated acute myeloid leukemia (HIV-AML), but karyotype, which is the best predictor of survival in AML, has not been evaluated in HIV-AML patients. A retrospective cohort of 31 patients was created from 9 local cases and 22 published cases. HIV-AML karyotypes were heterogeneous and were similar in distribution to those in HIV-negative AML. Among intensively treated patients, most achieved complete remission, but succumbed to infectious complications, mostly non-opportunistic, during consolidation therapy. Median survival for intensively-treated patients with CD4 counts <= 200 X 10(6) cells/L was 8.5 months, compared to 48 months for those with > 200 X 10(6) CD4 cells/L (p = 0.03). In contrast, AML karyotype did not predict survival (p = 0.43), albeit with small numbers in each karyotype group. Thus, CD4 count is a strong predictor of short survival in HIV-AML patients regardless of karyotype. Studies evaluating innovative strategies for infection prophylaxis and for improving immune reconstitution are needed.
引用
收藏
页码:660 / 664
页数:5
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