Human Immunodeficiency Virus Infection and Non-small Cell Lung Cancer: Survival and Toxicity of Antineoplastic Chemotherapy in a Cohort Study
Pulmonary and Respiratory Medicine
Adult
Male
HAART
Lung Neoplasms
Interaction
Anti-HIV Agents
Antineoplastic Agents
HIV Infections
NSCLC
03 medical and health sciences
0302 clinical medicine
Antiretroviral Therapy, Highly Active
Carcinoma, Non-Small-Cell Lung
Chemotherapy
Humans
Drug Interactions
Aged
Retrospective Studies
Toxicity
HIV
Middle Aged
Prognosis
Survival Analysis
Antiretroviral therapy
CD4 Lymphocyte Count
3. Good health
CD4 lymphocytes
Treatment Outcome
Oncology
Female
France
Lung cancer
DOI:
10.1097/jto.0b013e318217b6e0
Publication Date:
2011-04-21T07:34:24Z
AUTHORS (12)
ABSTRACT
To describe factors associated with survival in human immunodeficiency virus (HIV)-infected subjects with non-small cell lung cancer (NSCLC) and analyze toxicities induced by cytotoxic chemotherapy and antiretroviral compounds.Retrospective analyses of HIV-infected subjects with NSCLC enrolled in the Dat'Aids cohort. A toxicity substudy included subjects treated by at least one cycle of cytotoxic chemotherapy.Survival was analyzed using Cox models. In the toxicity substudy, factors associated with grade 4 hematological toxicity of each episode of combination of antiretroviral drugs and cytotoxic chemotherapy were analyzed using marginal logistic regression models.Fifty-two subjects were included in the study: 42 were men, median age was 48 years, 98% were smokers, with a median of 30 pack years, median CD4 was 300 cells/μl, and median survival time was 12 months. CD4 levels ≥200 cells/μl at NSCLC diagnosis (hazard ratio [HR] = 0.29, 95% confidence interval [CI] [0.10-0.89]), performance status less than 2 (HR = 0.32, 95% CI [0.15-0.68]) and highly active antiretroviral therapy (HR = 0.26, 95% CI [0.09-0.74]) were significantly associated with increased survival in the multivariable model. Forty subjects were included in the toxicity substudy, and 14 among 68 different combinations were complicated by a grade 4 hematological toxicity. Protease inhibitor use (odds ratio = 5.22, 95% CI [1.07-25.38]) was significantly associated with grade 4 hematological toxicity in the multivariable analyses.In HIV-infected patients, CD4 levels at NSCLC diagnosis may be a predictive factor of survival. Use of highly active antiretroviral therapy during NSCLC chemotherapy is warranted, but protease inhibitors should be used with caution, as they may enhance severe hematological toxicities.
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