Identifying patients with chronic lymphocytic leukemia without need of treatment: End of endless watch and wait?

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  • Christian Brieghel
  • Veerle Galle
  • Rudi Agius
  • Caspar da Cunha-Bang
  • Michael A Andersen
  • Philip Vlummens
  • Mattias Mattsson
  • Richard Rosenquist
  • Karin E Smedby
  • Carmen D Herling
  • Jasmin Bahlo
  • Michael Hallek
  • Lundgren, Jens
  • Fritz Offner
  • Niemann, Carsten

INTRODUCTION: Early-stage chronic lymphocytic leukemia (CLL) challenges specialized management and follow-up.

METHODS: We developed and validated a prognostic index to identify newly diagnosed patients without need of treatment (CLL-WONT) by a training/validation approach using data on 4708 patients. Composite scores derived from weighted hazards by multivariable analysis defined CLL-WONT risk groups.

RESULTS: Age (>65 years: 1 point), Binet stage (B: 2 points), lactate dehydrogenase (LDH) (>205 U/L: 1 point), absolute lymphocyte count (15-30 × 109 /L: 1 point; >30 × 109 /L; 2 points), β2-microglobulin (>4 mg/L: 1 point), IGHV mutation status (unmutated: 1 point), and 11q or 17p deletion (1 point) were independently associated with shorter time to first treatment (TTFT). Low-risk patients demonstrated 5-year TTFT of 2% by internal validation, but 7-19% by external validation. Including all patients with complete scores, the 5-year TTFT was 10% for the 756 (39%) CLL-WONT low-risk patients, and the 704 (37%) patients who were both CLL-WONT and CLL-IPI low risk demonstrated even lower 5-year TTFT (8%).

CONCLUSION: We have adopted the CLL-WONT at an institution covering 1 800 000 individuals to allow patients with both low-risk CLL-WONT and CLL-IPI to be managed by primary healthcare providers, thereby prioritizing specialized hematology services for patients in dire need.

Original languageEnglish
Book seriesEuropean Journal of Haematology
Volume108
Issue number5
Pages (from-to)369-378
Number of pages10
ISSN0902-4441
DOIs
Publication statusPublished - 2022

Bibliographical note

© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

    Research areas

  • Aged, Chromosome Aberrations, Humans, Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis, Mutation, Prognosis, Risk Factors

ID: 307913295