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Identifying patients with chronic lymphocytic leukemia without need of treatment: End of endless watch and wait?
Brieghel, Christian; Galle, Veerle; Agius, Rudi; da Cunha-Bang, Caspar; Andersen, Michael A; Vlummens, Philip; Mattsson, Mattias; Rosenquist, Richard; Smedby, Karin E; Herling, Carmen D; Bahlo, Jasmin; Hallek, Michael; Lundgren, Jens D; Offner, Fritz; Niemann, Carsten U.
Afiliação
  • Brieghel C; Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
  • Galle V; Department of Clinical Hematology, Ghent University Hospital, Ghent, Belgium.
  • Agius R; Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
  • da Cunha-Bang C; Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
  • Andersen MA; Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
  • Vlummens P; Department of Clinical Hematology, Ghent University Hospital, Ghent, Belgium.
  • Mattsson M; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
  • Rosenquist R; Department of Hematology, Uppsala University Hospital, Uppsala, Sweden.
  • Smedby KE; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Herling CD; Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.
  • Bahlo J; Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Hallek M; Department of Internal Medicine, Uniklinik Köln, Cologne, Germany.
  • Lundgren JD; Department of Internal Medicine, Uniklinik Köln, Cologne, Germany.
  • Offner F; Department of Internal Medicine, Uniklinik Köln, Cologne, Germany.
  • Niemann CU; Centre for Health, Immunity and Infectious Diseases (CHIP), Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Eur J Haematol ; 108(5): 369-378, 2022 May.
Article em En | MEDLINE | ID: mdl-35030282
ABSTRACT

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), ß2-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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article