International consensus statement on diagnosis, evaluation, and research of Richter transformation: the ERIC recommendations

  • Adam S. Kittai
  • , Monia Marchetti
  • , Othman Al-Sawaf
  • , Ohad Benjamini
  • , Alexey V. Danilov
  • , Matthew S. Davids
  • , Barbara Eichhorst
  • , Toby A. Eyre
  • , Anna Maria Frustaci
  • , Michael Hallek
  • , Paul J. Hampel
  • , Yair Herishanu
  • , Rodney J. Hicks
  • , Arnon P. Kater
  • , Rebecca L. King
  • , Jose I. Martin-Subero
  • , Carolyn Owen
  • , Erin Parry
  • , Maurilio Ponzoni
  • , Davide Rossi
  • Tanya Siddiqi, Stephan Stilgenbauer, Constantine S. Tam, Elisa ten Hacken, Philip A. Thompson, William Wierda, Gianluca Gaidano, Jennifer A. Woyach, Paolo Ghia

Risultato della ricerca: Contributo su rivistaCommento

Abstract

Richter transformation (RT) is defined as an aggressive lymphoma emerging in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL). Despite novel therapeutics developed in CLL, RT is associated with poor outcomes. In light of recent progress regarding the diagnostic procedures and therapeutic concepts of RT, an international group of experts, under the coordination of the European Research Initiative on CLL, has developed consensus recommendations for clinical procedures and future research on this disease. Patients with RT typically present with a rapid clinical decline, worsening B-symptoms, elevated lactate dehydrogenase, and/or rapidly enlarging lymphadenopathy. Workup should include a positron emission tomography–computed tomography scan for patients with suspected RT. An excisional biopsy should be taken from an accessible lesion, preferably with the highest fluorodeoxyglucose avidity, and analyzed for the presence of aggressive lymphoma. The molecular relationship to the original CLL clone(s) should be defined. Because no effective standard treatment for RT exists, patients should be treated in a clinical trial. Response of both RT and CLL should be assessed at an early time point, and survival end points should be prioritized in trial design. We hope that these recommendations can help to harmonize clinical and translational research and improve outcomes for patients with RT.

Lingua originaleInglese
pagine (da-a)291-303
Numero di pagine13
RivistaBlood
Volume146
Numero di pubblicazione3
DOI
Stato di pubblicazionePubblicato - 17 lug 2025

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