TY - JOUR
T1 - Response-Adapted Postinduction Strategy in Patients With Advanced-Stage Follicular Lymphoma
T2 - The FOLL12 Study
AU - Luminari, Stefano
AU - Manni, Martina
AU - Galimberti, Sara
AU - Versari, Annibale
AU - Tucci, Alessandra
AU - Boccomini, Carola
AU - Farina, Lucia
AU - Olivieri, Jacopo
AU - Marcheselli, Luigi
AU - Guerra, Luca
AU - Ferrero, Simone
AU - Arcaini, Luca
AU - Cavallo, Federica
AU - Kovalchuk, Sofya
AU - Skrypets, Tetiana
AU - del Giudice, Ilaria
AU - Chauvie, Stephane
AU - Patti, Caterina
AU - Stelitano, Caterina
AU - Ricci, Francesca
AU - Pinto, Antonello
AU - Casaluci, Gloria Margiotta
AU - Zilioli, Vittorio R.
AU - Merli, Anna
AU - Ladetto, Marco
AU - Bolis, Silvia
AU - Pavone, Vincenzo
AU - Chiarenza, Annalisa
AU - Arcari, Annalisa
AU - Anastasia, Antonella
AU - Dondi, Alessandra
AU - Mannina, Donato
N1 - Publisher Copyright:
© 2021 by American Society of Clinical Oncology.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - PURPOSE We compared 2 years of rituximab maintenance (RM) with a response-adapted postinduction approach in patients with follicular lymphoma who responded to induction immunochemotherapy. METHODS We randomly assigned treatment-naive, advanced-stage, high-tumor burden follicular lymphoma patients to receive standard RM or a response-adapted postinduction approach on the basis of metabolic response and molecular assessment of minimal residual disease (MRD). The experimental arm used three types of postinduction therapies: for complete metabolic response (CMR) and MRD-negative patients, observation; for CMR and MRD-positive (end of induction or follow-up) patients, four doses of rituximab (one per week, maximum three courses) until MRD-negative; and for non-CMR patients, one dose of ibritumomab tiuxetan followed by standard RM. The study was designed as noninferiority trial with progression-free survival (PFS) as the primary end point. RESULTS Overall, 807 patients were randomly assigned. After a median follow-up of 53 months (range, 1-92 months), patients in the standard arm had a significantly better PFS than those in the experimental arm (3-year PFS 86% v 72%; P < .001). The better PFS of the standard versus experimental arm was confirmed in all the study subgroups except non-CMR patients (n =65; P = .274). The 3-year overall survival was 98% (95% CI, 96 to 99) and 97% (95% CI, 95 to 99) in the reference and experimental arms, respectively (P = .238). CONCLUSION A metabolic and molecular response-adapted therapy as assessed in the FOLL12 study was associated with significantly inferior PFS compared with 2-year RM. The better efficacy of standard RM was confirmed in the subgroup analysis and particularly for patients achieving both CMR and MRDnegative.
AB - PURPOSE We compared 2 years of rituximab maintenance (RM) with a response-adapted postinduction approach in patients with follicular lymphoma who responded to induction immunochemotherapy. METHODS We randomly assigned treatment-naive, advanced-stage, high-tumor burden follicular lymphoma patients to receive standard RM or a response-adapted postinduction approach on the basis of metabolic response and molecular assessment of minimal residual disease (MRD). The experimental arm used three types of postinduction therapies: for complete metabolic response (CMR) and MRD-negative patients, observation; for CMR and MRD-positive (end of induction or follow-up) patients, four doses of rituximab (one per week, maximum three courses) until MRD-negative; and for non-CMR patients, one dose of ibritumomab tiuxetan followed by standard RM. The study was designed as noninferiority trial with progression-free survival (PFS) as the primary end point. RESULTS Overall, 807 patients were randomly assigned. After a median follow-up of 53 months (range, 1-92 months), patients in the standard arm had a significantly better PFS than those in the experimental arm (3-year PFS 86% v 72%; P < .001). The better PFS of the standard versus experimental arm was confirmed in all the study subgroups except non-CMR patients (n =65; P = .274). The 3-year overall survival was 98% (95% CI, 96 to 99) and 97% (95% CI, 95 to 99) in the reference and experimental arms, respectively (P = .238). CONCLUSION A metabolic and molecular response-adapted therapy as assessed in the FOLL12 study was associated with significantly inferior PFS compared with 2-year RM. The better efficacy of standard RM was confirmed in the subgroup analysis and particularly for patients achieving both CMR and MRDnegative.
UR - http://www.scopus.com/inward/record.url?scp=85125289146&partnerID=8YFLogxK
U2 - 10.1200/JCO.21.01234
DO - 10.1200/JCO.21.01234
M3 - Article
SN - 0732-183X
VL - 40
SP - 729
EP - 739
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 7
ER -