Safety and efficacy of cyclophosphamide, adriamycin, vincristine, prednisone and rituximab in patients with human immunodeficiency virus-associated diffuse large B-cell lymphoma: results of a phase II trial |
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Authors: | Ribera Josep-Maria,Oriol Albert,Morgades Mireia,González-Barca Eva,Miralles Pilar,López-Guillermo Armando,Gardella Santiago,López Andres,Abella Eugenia,García Marta PETHEMA, GELTAMO, GELCAB GESIDA Groups |
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Affiliation: | Haematology Department, Institut Catalàd'Oncologia-Hospital Universitari Germans Trias i Pujol, Badalona;, Haematology Department, Institut Catalàd'Oncologia-HospitalIDuran y Reynals, L'Hospitalet de Llobregat, Barcelona;, Infectious Diseases Department, Hospital Gregorio Marañón, Madrid;, Haematology Department, Hospital Clinic, Barcelona;, Haematology Department, Institut Catalàd'Oncologia-Hospital Josep Trueta, Girona;, Haematology Department, Hospital Vall d'Hebron, Barcelona;, Haematology Department, Hospital del Mar, Barcelona;, and Haematology Department, Consorci Hospitalari, Terrassa, Spain |
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Abstract: | Immunochemotherapy with cyclophosphamide, adriamycin, vincristine, prednisone and rituximab (R-CHOP) is the standard treatment in non-immunosuppressed patients with diffuse large B-cell lymphoma (DLBCL), but its adequacy has not been definitively established in patients with human immunodeficiency virus (HIV)-related lymphoma. This phase II trial aimed to evaluate the safety and efficacy of six cycles of R-CHOP in patients with HIV-related DLBCL and to determine whether response to highly active antiretroviral therapy (HAART) had prognostic impact. Patients were eligible if they had performance status <3 and absence of active opportunistic infections. Eighty-one patients were enrolled, 57 in stages III or IV, International Prognostic Index (IPI) 0 or 1 ( n = 26), 2 ( n = 19), 3 ( n = 20) and 4 or 5 ( n = 16), and median CD4 lymphocyte count of 0·158 × 109/l. The main adverse events were neutropenia (48% of cycles) and infections (10% of cycles), which were fatal in seven patients. Complete response was achieved in 55 (69%) patients, with an estimated 3-year disease-free survival of 77% and 3-year overall survival of 56%. IPI score and virological response to HAART were the prognostic parameters for response and survival. In HIV-related DLBCL R-CHOP is feasible, safe and effective. The prognosis depends on lymphoma-related parameters and on the response to HAART. |
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Keywords: | HIV-related diffuse large B-cell lymphoma CHOP rituximab highly active antiretroviral therapy virological response |
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