Consensus opinion from an international group of experts on measurable residual disease in hairy cell leukemia
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Published:2022-12-13
Issue:12
Volume:12
Page:
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ISSN:2044-5385
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Container-title:Blood Cancer Journal
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language:en
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Short-container-title:Blood Cancer J.
Author:
Ravandi FarhadORCID, Kreitman Robert J., Tiacci Enrico, Andritsos Leslie, Banerji Versha, Barrientos Jacqueline C., Bhat Seema A., Blachly James S.ORCID, Broccoli AlessandroORCID, Call Timothy, Chihara DaiORCID, Dearden Claire, Demeter JuditORCID, Dietrich SashaORCID, Else MonicaORCID, Epperla NarendranathORCID, Falini BrunangeloORCID, Forconi FrancescoORCID, Gladstone Douglas E., Gozzetti AlessandroORCID, Iyengar Sunil, Johnston James B., Jorgensen JeffreyORCID, Juliusson Gunnar, Lauria Francesco, Lozanski Gerard, Parikh Sameer A.ORCID, Park Jae H.ORCID, Polliack Aaron, Quest Graeme, Robak TadeuszORCID, Rogers Kerry A., Saven Alan, Seymour John F.ORCID, Tadmor TamarORCID, Tallman Martin S., Tam Constantine S., Thompson Philip A.ORCID, Troussard Xavier, Zent Clive S.ORCID, Zenz ThorstenORCID, Zinzani Pier LuigiORCID, Wörmann BernhardORCID, Rai KantiORCID, Grever Michael
Abstract
AbstractA significant body of literature has been generated related to the detection of measurable residual disease (MRD) at the time of achieving complete remission (CR) in patients with hairy cell leukemia (HCL). However, due to the indolent nature of the disease as well as reports suggesting long-term survival in patients treated with a single course of a nucleoside analog albeit without evidence of cure, the merits of detection of MRD and attempts to eradicate it have been debated. Studies utilizing novel strategies in the relapse setting have demonstrated the utility of achieving CR with undetectable MRD (uMRD) in prolonging the duration of remission. Several assays including immunohistochemical analysis of bone marrow specimens, multi-parameter flow cytometry and molecular assays to detect the mutant BRAF V600E gene or the consensus primer for the immunoglobulin heavy chain gene (IGH) rearrangement have been utilized with few comparative studies. Here we provide a consensus report on the available data, the potential merits of MRD assessment in the front-line and relapse settings and recommendations on future role of MRD assessment in HCL.
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Hematology
Reference47 articles.
1. Luskin MR, Murakami MA, Manalis SR, Weinstock DM. Targeting minimal residual disease: a path to cure? Nat Rev Cancer. 2018;18:255–63. 2. Heuser M, Freeman SD, Ossenkoppele GJ, Buccisano F, Hourigan CS, Ngai LL, et al. 2021 update measurable residual disease in acute myeloid leukemia: European LeukemiaNet Working Party Consensus Document. Blood. 2021;138:2753–2767. 3. Gokbuget N, Dombret H, Bonifacio M, Reichle A, Graux C, Faul C, et al. Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia. Blood. 2018;131:1522–31. 4. Short NJ, Jabbour E, Sasaki K, Patel K, O’Brien SM, Cortes JE, et al. Impact of complete molecular response on survival in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood. 2016;128:504–7. 5. Etienne G, Guilhot J, Rea D, Rigal-Huguet F, Nicolini F, Charbonnier A, et al. Long-Term Follow-Up of the French Stop Imatinib (STIM1) study in patients with chronic myeloid leukemia. J Clin Oncol. 2017;35:298–305.
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