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Related Experiment Video

Updated: Jun 20, 2026

Identification of Quiescent Cells in a Zebrafish T-Cell Acute Lymphoblastic Leukemia Model Using Cell Proliferation Staining
06:41

Identification of Quiescent Cells in a Zebrafish T-Cell Acute Lymphoblastic Leukemia Model Using Cell Proliferation Staining

Published on: July 19, 2024

T-cell prolymphocytic leukemia.

Claire E Dearden1

  • 1Department of Haemato-Oncology, The Royal Marsden Hospital and Institute of Cancer Research, Sutton, Surrey SM2 5PT, United Kingdom. claire.dearden@rmh.nhs.uk

Clinical Lymphoma & Myeloma
|September 26, 2009
PubMed
Summary

T-cell prolymphocytic leukemia (T-PLL) is an aggressive cancer. While purine analogues and alemtuzumab improve outcomes, allogeneic stem cell transplantation offers the only cure, with newer methods expanding eligibility.

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Guideline for the treatment of chronic lymphocytic leukaemia: A British Society for Haematology Guideline.

British journal of haematology·2018
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Epidemiology and environmental aspects of marginal zone lymphomas.

Best practice & research. Clinical haematology·2017
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The efficacy and tolerability of pomalidomide in relapsed/refractory myeloma patients in a "real-world" study: the Royal Marsden Hospital experience.

Leukemia & lymphoma·2016
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Long-term follow-up after purine analogue therapy in hairy cell leukaemia.

Best practice & research. Clinical haematology·2015
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An unusual indication for splenectomy in hairy cell leukaemia: a report of three cases with persistent splenomegaly after chemoimmunotherapy.

British journal of haematology·2015
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Rituximab plus chlorambucil as first-line treatment for chronic lymphocytic leukemia: Final analysis of an open-label phase II study.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology·2014

Area of Science:

  • Hematology
  • Oncology

Background:

  • T-cell prolymphocytic leukemia (T-PLL) is a rare postthymic malignancy.
  • T-PLL is characterized by aggressive clinical course, poor response to conventional chemotherapy, and short survival.

Purpose of the Study:

  • To summarize the clinical features, treatment outcomes, and therapeutic advancements in T-cell prolymphocytic leukemia.

Main Methods:

  • Review of clinical, morphologic, immunophenotypic, and cytogenetic features.
  • Analysis of treatment responses to purine analogues, alemtuzumab, and stem cell transplantation.

Main Results:

  • Purine analogues and alemtuzumab demonstrate higher response rates and improved survival compared to conventional chemotherapy.
  • Allogeneic stem cell transplantation remains the only potentially curative treatment for T-PLL.

Conclusions:

  • While newer transplant methods like nonmyeloablative transplantation are expanding eligibility, T-PLL remains a challenging malignancy requiring further therapeutic innovation.

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Last Updated: Jun 20, 2026

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