TY - JOUR
T1 - Randomized phase 3 study in low-grade lymphoma comparing maintenance anti-CD20 antibody with observation after induction therapy
T2 - A trial of the ECOG-ACRIN cancer research group (E1496)
AU - Barta, Stefan K.
AU - Li, Hailun
AU - Hochster, Howard S.
AU - Hong, Fangxin
AU - Weller, Edie
AU - Gascoyne, Randy D.
AU - Habermann, Thomas M.
AU - Gordon, Leo I.
AU - Colocci, Natalia
AU - Bengtson, Elizabeth M.
AU - Horning, Sandra J.
AU - Kahl, Brad S.
N1 - Funding Information:
This study was coordinated by the ECOG-ACRIN Cancer Research Group (Robert L. Comis, MD, and Mitchell D. Schnall, MD, PhD, group cochairs) and was supported in part by the Public Health Service (grants CA180794, CA180820, CA180826, CA180790, CA180816, CA180799, and CA180821) and the National Cancer Institute (National Institutes of Health, US Department of Health and Human Services). The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the National Cancer Institute.
Funding Information:
Stefan K. Barta reports grants and personal fees from Seattle Genetics, grants from Merck, grants and personal fees from Celgene, and personal fees from Pharmacyclics outside the submitted work. Howard S. Hochster reports working as a consultant for Bayer, Genentech, Genomic Health, and Bristol-Myers Squibb. Sandra J. Horning reports employment by Roche, ownership of Roche stock, and employment by Genentech. Brad S. Kahl reports research funding from and consulting work for Genentech.
Publisher Copyright:
© 2016 American Cancer Society.
PY - 2016/10
Y1 - 2016/10
N2 - BACKGROUND: In an ECOG-ACRIN Cancer Research Group study (E1496), maintenance rituximab (MR) was reported to prolong progression-free survival (PFS) in comparison with observation (OBS) alone in patients with indolent lymphoma after induction chemotherapy. Here the long-term follow-up of the same patient cohort is presented. METHODS: Patients with indolent lymphoma received induction chemotherapy with cyclophosphamide, vincristine, and prednisone (CVP). Patients with stable disease or a better response were then randomized to weekly rituximab (375 mg/m2 × 4 doses) every 6 months for 2 years (MR) or to OBS. The primary endpoint was PFS; the secondary endpoints were overall survival (OS), response rate, and toxicities. RESULTS: Of the 387 patients who initially received CVP induction, 158 were randomized to MR, and 153 were randomized to OBS. After a median follow-up of 11.5 years, patients on MR had longer median PFS (4.8 years) than patients on OBS (1.3 years; hazard ratio [HR], 0.49; P <.0001). However, there was no difference in OS between MR and OBS (10-year OS, 67% vs 59%; median OS, 13.5 years vs not reached; HR, 0.91; P = .69). Other than MR, only minimal residual disease after induction therapy was significantly associated with PFS on multivariate analysis (HR, 0.71; P = .02). A low initial tumor burden, minimal residual disease, follicular histology, a low Follicular Lymphoma International Prognostic Index score, and female sex were associated with longer OS. There was no increase in the rate of second primary malignancies with MR vs OBS. CONCLUSIONS: With long-term follow-up, MR did not influence OS. The PFS benefit was maintained. MR should be considered optional for patients with indolent B-cell lymphoma.
AB - BACKGROUND: In an ECOG-ACRIN Cancer Research Group study (E1496), maintenance rituximab (MR) was reported to prolong progression-free survival (PFS) in comparison with observation (OBS) alone in patients with indolent lymphoma after induction chemotherapy. Here the long-term follow-up of the same patient cohort is presented. METHODS: Patients with indolent lymphoma received induction chemotherapy with cyclophosphamide, vincristine, and prednisone (CVP). Patients with stable disease or a better response were then randomized to weekly rituximab (375 mg/m2 × 4 doses) every 6 months for 2 years (MR) or to OBS. The primary endpoint was PFS; the secondary endpoints were overall survival (OS), response rate, and toxicities. RESULTS: Of the 387 patients who initially received CVP induction, 158 were randomized to MR, and 153 were randomized to OBS. After a median follow-up of 11.5 years, patients on MR had longer median PFS (4.8 years) than patients on OBS (1.3 years; hazard ratio [HR], 0.49; P <.0001). However, there was no difference in OS between MR and OBS (10-year OS, 67% vs 59%; median OS, 13.5 years vs not reached; HR, 0.91; P = .69). Other than MR, only minimal residual disease after induction therapy was significantly associated with PFS on multivariate analysis (HR, 0.71; P = .02). A low initial tumor burden, minimal residual disease, follicular histology, a low Follicular Lymphoma International Prognostic Index score, and female sex were associated with longer OS. There was no increase in the rate of second primary malignancies with MR vs OBS. CONCLUSIONS: With long-term follow-up, MR did not influence OS. The PFS benefit was maintained. MR should be considered optional for patients with indolent B-cell lymphoma.
KW - Follicular lymphoma
KW - Indolent lymphoma
KW - Non-hodgkin lymphoma
KW - Rituximab
KW - Rituximab maintenance
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U2 - 10.1002/cncr.30137
DO - 10.1002/cncr.30137
M3 - Article
C2 - 27351685
AN - SCOPUS:84994372777
SN - 0008-543X
VL - 122
SP - 2996
EP - 3004
JO - Cancer
JF - Cancer
IS - 19
ER -