ADULT;
AGED;
ALOPECIA;
BLOOD TOXICITY;
BONE MARROW BIOPSY;
CANCER COMBINATION CHEMOTHERAPY;
CANCER MORTALITY;
CANCER SURVIVAL;
CENTRAL NERVOUS SYSTEM INFECTION;
CLINICAL ARTICLE;
CLINICAL TRIAL;
DIGESTIVE SYSTEM PERFORATION;
DISEASE ASSOCIATION;
DISEASE COURSE;
DOSE RESPONSE;
DRUG DOSE REGIMEN;
DRUG EFFICACY;
DRUG MEGADOSE;
DRUG RESPONSE;
DRUG SAFETY;
DRUG TOLERABILITY;
DRUG TOLERANCE;
FEBRILE NEUTROPENIA;
FEMALE;
GASTROINTESTINAL HEMORRHAGE;
HIGHLY ACTIVE ANTIRETROVIRAL THERAPY;
HISTOPATHOLOGY;
HUMAN;
HUMAN IMMUNODEFICIENCY VIRUS INFECTION;
MALE;
MULTICENTER STUDY;
MYCOSIS;
NAUSEA AND VOMITING;
NONHODGKIN LYMPHOMA;
PHASE 1 CLINICAL TRIAL;
PHASE 2 CLINICAL TRIAL;
PNEUMOCYSTOSIS;
REVIEW;
SINGLE DRUG DOSE;
SURVIVAL RATE;
THROMBOCYTOPENIA;
TREATMENT OUTCOME;
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Highly active antiretroviral therapy and incidence of cancer in human immunodeficiency virus-infected adults
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Low-dose compared with standard-dose m-BACOD chemotherapy for non-Hodgkin's lymphoma associated with human immunodeficiency virus infection
National Institute of Allergy and Infectious Diseases AIDS Clinical Trials Group
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The International Prognostic Index can be used as a guide to treatment decisions regarding patients with human immunodeficiency virus-related systemic non-Hodgkin lymphoma
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Influence of highly active anti-retroviral therapy on response to treatment and survival in patients with acquired immunodeficiency syndrome-related non-Hodgkin's lymphoma treated with cyclophosphamide, hydroxydoxorubicin, vincristine and prednisone
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