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Response-adapted therapy with infusional EPOCH chemotherapy plus rituximab in HIV-associated, B-cell non-Hodgkin's lymphoma.
Sparano, Joseph A; Lee, Jeannette Y; Kaplan, Lawrence D; Ramos, Juan Carlos; Ambinder, Richard F; Wachsman, William; Aboulafia, David; Noy, Ariela; Henry, David H; Ratner, Lee; Cesarman, Ethel; Chadburn, Amy; Mitsuyasu, Ronald.
Afiliação
  • Sparano JA; Montefiore-Einstein Cancer Center, Montefiore Medical Center, Bronx, NY, USA.
  • Lee JY; University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Kaplan LD; University of California, San Francisco, San Francisco, CA, USA.
  • Ramos JC; University of Miami, Sylvester Comprehensive Cancer Center, Miami, USA.
  • Ambinder RF; Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, MD, USA.
  • Wachsman W; Moores University of California, San Diego Cancer Center, La Jolla, CA, USA.
  • Aboulafia D; Virginia Mason Cancer Institute, Seattle, WA, USA.
  • Noy A; Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA.
  • Henry DH; University of Pennsylvania, Pennsylvania Hospital, Philadelphia, PA, USA.
  • Ratner L; Washington University, St. Louis, MO, USA.
  • Cesarman E; Weill Medical College of Cornell University, New York, NY, USA.
  • Chadburn A; Weill Cornell Medical College, New York, NY, USA.
  • Mitsuyasu R; University of California, Los Angeles Medical Center, Los Angeles, CA, USA.
Haematologica ; 106(3): 730-735, 2021 03 01.
Article em En | MEDLINE | ID: mdl-32107337
ABSTRACT
Four cycles of rituximab plus CHOP chemotherapy is as effective as 6 cycles in low-risk diffuse large B-cell lymphoma (DLBCL). Here we report a post-hoc analysis of a prospective clinical trial in patients with HIV-associated DLBCL and high-grade lymphoma treated with 4-6 cycles of EPOCH plus rituximab based a response-adapted treatment strategy. 106 evaluable patients with HIV-associated DLBCL or high-grade CD20-positive non-Hodgkin's lymphoma were randomized to receive rituximab (375 mg/m2) given either concurrently prior to each infusional EPOCH cycle, or sequentially (weekly for 6 weeks) following completion of EPOCH. EPOCH consisted of a 96-hour IV infusion of etoposide, doxorubicin, and vincristine plus oral prednisone followed by IV bolus cyclophosphamide every 21 days for 4 to 6 cycles. Patients received 2 additional cycles of therapy after documentation of a complete response (CR) by computerized tomography after cycles 2 and 4. 64 of 106 evaluable patients (60%, 95% CI 50%, 70%) had a CR in both treatment arms. The 2-year event-free survival (EFS) rates were similar in the 24 patients with CR who received 4 or fewer EPOCH cycles (78%, 95% confidence intervals [55%, 90%]) due to achieving a CR after 2 cycles, compared with those who received 5-6 cycles of EPOCH (85%, 95% CI 70%, 93%) because a CR was first documented after cycle 4. A response-adapted strategy may permit a shorter treatment duration without compromising therapeutic efficacy in patients with HIV-associated lymphoma treated with EPOCH plus rituximab, which merits further evaluation in additional prospective trials. Clinical Trials.gov identifier NCT00049036.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Infecções por HIV / Linfoma Difuso de Grandes Células B Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Infecções por HIV / Linfoma Difuso de Grandes Células B Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article