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A fixed-duration, measurable residual disease–guided approach in CLL: follow-up data from the phase 2 ICLL-07 FILO trial
Author(s) -
AnneSophie Michallet,
Rémi Letestu,
Magali Le GarffTavernier,
Carmen Aanei,
Michel Ticchioni,
MarieSarah Dilhuydy,
Fabien Subtil,
Valérie Rouille,
Beatrice Mahé,
Kamel Laribi,
Bruno Villemagne,
Gilles Salles,
Olivier Tournilhac,
Alain Delmer,
Christelle Portois,
Brigitte Pegourié,
Véronique Leblond,
Cécile Tomowiak,
Sophie de Guibert,
Frédérique Orsini Piocelle,
Anne Banos,
P. Carassou,
Guillaume Cartron,
LucMatthieu Fornecker,
Loïc Ysebaert,
Caroline Dartigeas,
Malgorzata Truchan-Graczyk,
JeanPierre Vilque,
Thérèse Aurran,
Florence Cymbalista,
Stéphane Leprêtre,
Vincent Lévy,
Florence NguyenKhac,
Pierre Feugier
Publication year - 2020
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood.2020008164
Subject(s) - medicine , fludarabine , obinutuzumab , minimal residual disease , cyclophosphamide , ibrutinib , surgery , hazard ratio , confidence interval , median follow up , peripheral edema , adverse effect , chronic lymphocytic leukemia , bone marrow , leukemia , gastroenterology , oncology , chemotherapy
Trials assessing first-line, fixed-duration approaches in chronic lymphocytic leukemia (CLL) are yielding promising activity, but few long-term data are available. We report follow-up data from a phase 2 trial (ICLL07 FILO) in previously untreated, medically fit patients (N = 135). Patients underwent obinutuzumab-ibrutinib induction for 9 months; then, following evaluation (N = 130 evaluable), those in complete remission and with bone marrow measurable residual disease (BM MRD) <0.01% (n = 10) received ibrutinib for 6 additional months; those in partial remission and/or with BM MRD ≥0.01%, the majority (n = 120), also received 4 cycles of immunochemotherapy (fludarabine/cyclophosphamide-obinutuzumab). Beyond end of treatment, responses were assessed every 3 month and peripheral blood MRD every 6 months. At median follow-up 36.7 months from treatment start, progression-free and overall survival rates (95% confidence interval) at 3 years were 95.7% (92.0% to 99.5%) and 98% (95.1% to 100%), respectively. Peripheral blood MRD <0.01% rates were 97%, 96%, 90%, 84%, and 89% at months 16, 22, 28, 34, and 40, respectively. No new treatment-related or serious adverse event occurred beyond end of treatment. Thus, in previously untreated, medically fit patients with CLL, a fixed-duration (15 months), MRD-guided approach achieved high survival rates, a persistent MRD benefit beyond the end of treatment, and low long-term toxicity. This trial was registered at www.clinicaltrials.gov as #NCT02666898.

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