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Gemcitabine and liposomal doxorubicin (GemDox) for the treatment of relapsed and refractory T-cell lymphomas

  • Zachary Braunstein
  • , Allyson Waller
  • , Emily Dotson
  • , Eric McLaughlin
  • , Walter Hanel
  • , John Reneau
  • , Daniel Addison
  • , Pierluigi Porcu
  • , Jonathan Edward Brammer

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Aggressive T-cell lymphomas (TCL) account for 10–15% of non-Hodgkin lymphomas (NHL) with weaker responses and shorter durations to chemotherapy than other types of NHL. Current therapies for patients with relapsed/refractory Cutaneous T-cell lymphoma (CTCL) have limited efficacy, and short durations of response. Gemcitabine and liposomal doxorubicin have shown single-agent activity in TCL and combined have activity in relapsed B-cell lymphomas. We evaluated outcomes of 18 patients with relapsed/refractory aggressive TCL (13 CTCL, 5 PTCL) treated with a gemcitabine plus liposomal doxorubicin (GemDox) combination and evaluated outcomes with a specific focus on CTCL patients. Significant responses were observed in CTCL patients with an overall response rate of over 80%. In all patients, objective responses were seen in eight patients (50%), with six patients (5 CTCL) able to proceed to allogeneic stem cell transplant. Given limited treatment options for r/r CTCL, GemDox should be considered a therapeutic option in relapsed/refractory CTCL.

Original languageEnglish
Pages (from-to)301-311
Number of pages11
JournalLeukemia and Lymphoma
Volume65
Issue number3
DOIs
StatePublished - 2024

Bibliographical note

Publisher Copyright:
© 2023 Informa UK Limited, trading as Taylor & Francis Group.

Funding

The author(s) reported there is no funding associated with the work featured in this article.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Chemotherapeutic approaches
  • lymphoma and Hodgkin disease
  • pharmacotherapeutics

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

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