| Literature DB >> 33496747 |
François Lemonnier1,2, Violaine Safar3, Asma Beldi-Ferchiou2,4, Anne-Ségolène Cottereau5, Emmanuel Bachy3, Guillaume Cartron6, Virginie Fataccioli2,7, Laura Pelletier2, Cyrielle Robe2,7, Audrey Letourneau8, Edoardo Missiaglia8, Slim Fourati2,9, Marie-Pierre Moles-Moreau10, Alain Delmer11, Reda Bouabdallah12, Laurent Voillat13, Stéphanie Becker14, Céline Bossard15, Marie Parrens16, Olivier Casasnovas17, Victoria Cacheux18, Caroline Régny19, Vincent Camus20, Marie-Hélène Delfau-Larue2,4, Michel Meignan21, Laurence de Leval8, Philippe Gaulard2,7, Corinne Haioun1,2.
Abstract
Angioimmunoblastic T-cell lymphoma (AITL) is a frequent T-cell lymphoma in the elderly population that has a poor prognosis when treated with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy. Lenalidomide, which has been safely combined with CHOP to treat B-cell lymphoma, has shown efficacy as a single agent in AITL treatment. We performed a multicentric phase 2 trial combining 25 mg lenalidomide daily for 14 days per cycle with 8 cycles of CHOP21 in previously untreated AITL patients aged 60 to 80 years. The primary objective was the complete metabolic response (CMR) rate at the end of treatment. Seventy-eight of the 80 patients enrolled were included in the efficacy and safety analysis. CMR was achieved in 32 (41%; 95% confidence interval [CI], 30%-52.7%) patients, which was below the prespecified CMR rate of 55% defined as success in the study. The 2-year progression-free survival (PFS) was 42.1% (95% CI, 30.9%-52.8%), and the 2-year overall survival was 59.2% (95% CI, 47.3%-69.3%). The most common toxicities were hematologic and led to treatment discontinuation in 15% of patients. This large prospective and uniform series of AITL treatment data was used to perform an integrative analysis of clinical, pathologic, biologic, and molecular data. TET2, RHOA, DNMT3A, and IDH2 mutations were present in 78%, 54%, 32%, and 22% of patients, respectively. IDH2 mutations were associated with distinct pathologic and clinical features and DNMT3A was associated with shorter PFS. In conclusion, the combination of lenalidomide and CHOP did not improve the CMR in AITL patients. This trial clarified the clinical impact of recurrent mutations in AITL. This trial was registered at www.clincialtrials.gov as #NCT01553786.Entities:
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Year: 2021 PMID: 33496747 PMCID: PMC7839364 DOI: 10.1182/bloodadvances.2020003081
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529