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Romidepsin-Bendamustine Combination for Relapsed/Refractory T Cell Lymphoma.
Nachmias, Boaz; Shaulov, Adir; Lavie, David; Goldschmidt, Neta; Gural, Alexander; Saban, Revital; Lebel, Eyal; Gatt, Moshe E.
Afiliação
  • Nachmias B; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Shaulov A; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Lavie D; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Goldschmidt N; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Gural A; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Saban R; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Lebel E; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel.
  • Gatt ME; Department of Hematology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel, RMOSHG@hadassah.org.il.
Acta Haematol ; 141(4): 216-221, 2019.
Article em En | MEDLINE | ID: mdl-30943470
BACKGROUND: The treatment of relapsed/refractory (R/R) peripheral T cell lymphoma (PTCL) is limited to a few agents. Romidepsin, a histone deacetylase inhibitor, was approved for PTCL treatment as a single agent in the R/R setting, yet with partial efficacy. Several attempts to combine romidepsin with other chemotherapy regimens have been reported, however, with significant toxicity. OBJECTIVES: To study the romidepsin-bendamustine combination in PTCL in an attempt to maximize efficacy while minimizing toxicity. METHODS: We report on a series of 7 heavily pretreated PTCL patients (2-5 previous lines of therapy) treated with a romidepsin-bendamustine combination. RESULTS: Four patients were not previously exposed to either drug. Of these, 2 achieved complete remission. Interestingly, 1 patient continued treatment with a prolonged progression-free survival of more than 4 years. Toxicity was minimal and no treatment-related deaths or discontinuation were noted. Significant nausea and vomiting were reported in over 50% of patients. Hematological toxicity was mild and lower than that reported for other romidepsin-chemotherapy combinations and was correlated with bone marrow involvement by lymphoma. CONCLUSIONS: Although reporting a small number of patients, our data suggest that the combination of romidepsin and bendamustine may be a feasible therapeutic option in R/R PTCL patients and merits further study.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células T Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Acta Haematol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células T Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Acta Haematol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Israel