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Multicenter Study of Risk-Adapted Therapy With Dose-Adjusted EPOCH-R in Adults With Untreated Burkitt Lymphoma.
Roschewski, Mark; Dunleavy, Kieron; Abramson, Jeremy S; Powell, Bayard L; Link, Brian K; Patel, Prapti; Bierman, Philip J; Jagadeesh, Deepa; Mitsuyasu, Ronald T; Peace, David; Watson, Peter R; Hanna, Wahid T; Melani, Christopher; Lucas, Andrea N; Steinberg, Seth M; Pittaluga, Stefania; Jaffe, Elaine S; Friedberg, Jonathan W; Kahl, Brad S; Little, Richard F; Bartlett, Nancy L; Fanale, Michelle A; Noy, Ariela; Wilson, Wyndham H.
Afiliação
  • Roschewski M; Lymphoid Malignancies Branch, National Cancer Institute, Bethesda, MD.
  • Dunleavy K; George Washington University Cancer Center, Washington, DC.
  • Abramson JS; Massachusetts General Hospital Cancer Center, Boston, MA.
  • Powell BL; Comprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC.
  • Link BK; University of Iowa Hospital and Clinics, Iowa City, IA.
  • Patel P; University of Texas Southwestern, Dallas, TX.
  • Bierman PJ; University of Nebraska Medical Center, Omaha, NE.
  • Jagadeesh D; Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Mitsuyasu RT; University of California Los Angeles Clinical AIDS Research and Education Center, Los Angeles, CA.
  • Peace D; University of Illinois, Chicago, IL.
  • Watson PR; Kinston Medical Specialists, Kinston, NC.
  • Hanna WT; University of Tennessee Medical Center, Knoxville, TN.
  • Melani C; Lymphoid Malignancies Branch, National Cancer Institute, Bethesda, MD.
  • Lucas AN; Lymphoid Malignancies Branch, National Cancer Institute, Bethesda, MD.
  • Steinberg SM; Biostatistics and Data Management Section, Center for Cancer Research, National Cancer Institute, Bethesda, MD.
  • Pittaluga S; Hematopathology Section, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD.
  • Jaffe ES; Hematopathology Section, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD.
  • Friedberg JW; Montefiore Medical Center, Bronx, NY.
  • Kahl BS; Washington University School of Medicine, St. Louis, MO.
  • Little RF; Division of Cancer Therapy and Diagnosis, National Cancer Institute, Bethesda, MD.
  • Bartlett NL; Washington University School of Medicine, St. Louis, MO.
  • Fanale MA; MD Anderson Cancer Center, Houston, TX, and Seattle Genetics, Seattle, WA.
  • Noy A; Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY.
  • Wilson WH; Lymphoid Malignancies Branch, National Cancer Institute, Bethesda, MD.
J Clin Oncol ; 38(22): 2519-2529, 2020 08 01.
Article em En | MEDLINE | ID: mdl-32453640
PURPOSE: Burkitt lymphoma is an aggressive B-cell lymphoma curable with dose-intensive chemotherapy derived from pediatric leukemia regimens. Treatment is acutely toxic with late sequelae. We hypothesized that dose-adjusted etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone, and rituximab (DA-EPOCH-R) may obviate the need for highly dose-intensive chemotherapy in adults with Burkitt lymphoma. METHODS: We conducted a multicenter risk-adapted study of DA-EPOCH-R in untreated adult Burkitt lymphoma. Low-risk patients received three cycles without CNS prophylaxis, and high-risk patients received six cycles with intrathecal CNS prophylaxis or extended intrathecal treatment if leptomeninges were involved. The primary endpoint was event-free survival (EFS), and secondary endpoints were toxicity and predictors of EFS and overall survival (OS). RESULTS: Between 2010 and 2017, 113 patients were enrolled across 22 centers, and 98 (87%) were high risk. The median age was 49 (range, 18-86) years, and 62% were ≥ 40 years. Bone marrow and/or CSF was involved in 29 (26%) of patients, and 28 (25%) were HIV positive. At a median follow-up of 58.7 months, EFS and OS were 84.5% and 87.0%, respectively, and EFS was 100% and 82.1% in low- and high-risk patients. Therapy was equally effective across age groups, HIV status, and International Prognostic Index risk groups. Involvement of the CSF identified the group at greatest risk for early toxicity-related death or treatment failure. Five treatment-related deaths (4%) occurred during therapy. Febrile neutropenia occurred in 16% of cycles, and tumor lysis syndrome was rare. CONCLUSION: Risk-adapted DA-EPOCH-R therapy is effective in adult Burkitt lymphoma regardless of age or HIV status and was well tolerated. Improved therapeutic strategies for adults with CSF involvement are needed (funded by the National Cancer Institute; ClinicalTrials.gov identifier: NCT01092182).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Burkitt Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Burkitt Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article