Intensive sequential chemotherapy with hematopoietic growth factor support for non-Hodgkin lymphoma in patients infected with the human immunodeficiency virus
Autor: | Aude Charbonnier, Daniel Olive, Claude Alzieu, Gérard Lepeu, Rolande Cohen, Luc Xerri, Hacène Zerazhi, Isabelle Poizot-Martin, Régis Costello, Valérie-Jeanne Bardou, Jean-Albert Gastaut, Jean-Marc Schiano de Colella, Meyer Nezri |
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Rok vydání: | 2004 |
Předmět: |
Adult
Male Cancer Research Vincristine medicine.medical_specialty Anti-HIV Agents medicine.medical_treatment HIV Infections CHOP Gastroenterology Disease-Free Survival Drug Administration Schedule International Prognostic Index Internal medicine Antineoplastic Combined Chemotherapy Protocols Granulocyte Colony-Stimulating Factor medicine Humans Infusions Intravenous Cyclophosphamide Survival rate Chemotherapy Dose-Response Relationship Drug business.industry Lymphoma Non-Hodgkin Cytarabine Middle Aged Viral Load Prognosis CD4 Lymphocyte Count Regimen Methotrexate Treatment Outcome Oncology Doxorubicin Injections Intravenous Immunology Prednisone Female Radiotherapy Adjuvant business Viral load medicine.drug |
Zdroj: | Cancer. 100:667-676 |
ISSN: | 1097-0142 0008-543X |
Popis: | BACKGROUND Optimal treatment of human immunodeficiency virus (HIV)-associated non-Hodgkin lymphoma (NHL) has yet to be defined, because chemotherapy could exacerbate immunodeficiency, with subsequent adverse effects for patients. METHODS The authors investigated the feasibility of an intensive chemotherapy regimen for HIV-associated NHL. Thirty-eight patients were treated with a first course of cyclophosphamide (Cy), vincristine, and prednisone; followed by 3 courses of high-dose Cy (2000 mg/m2), doxorubicin (Doxo; 50 mg/m2), vincristine, and prednisone (modified high-dose CHOP); 1 course of high-dose methotrexate (MTX; 8000 mg/m2); and 1 course of high-dose cytarabine (8000 mg/m2). Radiotherapy was added to the treatment regimen for patients with bulky disease or residual tumor. Chemotherapy was administered in conjunction with granulocyte–colony-stimulating factor and antiretroviral therapy. RESULTS Patients received 91.5%, 93%, 66%, and 63% of the scheduled doses of Cy, Doxo, MTX, and cytarabine, respectively. The complete response rate was 60.5%, with a total response rate of 79%. The 40-month overall survival rate was 43%, the disease-free survival rate was 65%, and the recurrence-free survival rate was 39%. Both an International Prognostic Index score of 0 or 1 and Burkitt-type histology had positive effects on survival, whereas CD4-positive lymphocyte counts, viral burden, and previous highly active antiretroviral therapy did not. CD4-positive T lymphocyte levels decreased from 0.197 ± 0.156 ×109/L before treatment to 0.152 ± 0.1 ×109/L at 6 months after the end of treatment. A decrease in viral load, from 380,000 ± 785,000 copies/mL before treatment to 25,000 ± 43,000 copies/mL at 6 months after the end of treatment, also was observed. CONCLUSIONS The results of the current study indicate that intensive chemotherapy is effective and tolerable for patients with HIV-associated NHL. Cancer 2004;100:667–76. © 2004 American Cancer Society. |
Databáze: | OpenAIRE |
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