TY - JOUR
T1 - Durable benefit of rituximab maintenance post-autograft in patients with relapsed follicular lymphoma
T2 - 12-year follow-up of the EBMT lymphoma working party Lym1 trial
AU - Pettengell, R
AU - Uddin, R
AU - Boumendil, A
AU - Johnson, R
AU - Metzner, B
AU - Martín, A
AU - Romejko-Jarosinska, J
AU - Bence-Bruckler, I
AU - Giri, P
AU - Niemann, C U
AU - Robinson, S P
AU - Kimby, E
AU - Schmitz, N
AU - Dreger, P
AU - Goldstone, A H
AU - Montoto, S
PY - 2021/1
Y1 - 2021/1
N2 - We report the 12-year follow-up of the prospective randomized EBMT LYM1 trial to determine whether the benefit of brief duration rituximab maintenance (RM) on progression-free survival (PFS) in patients with relapsed follicular lymphoma (FL) receiving an autologous stem cell transplant (ASCT) is sustained. One hundred and thirty-eight patients received RM with or without purging. The median follow-up after random assignment is 12 years (range 10-13) for the whole series. The 10-year PFS after ASCT is 47% (95% CI 40-54) with only 4 patients relapsing after 7.5 years. RM continues to significantly improve 10-year PFS after ASCT in comparison with NM [P = 0.002; HR 0.548 (95% CI 0.38-0.80)]. Ten-year non-relapse mortality (NRM) was not significantly different between treatment groups (7% overall). 10-year overall survival (OS) after ASCT was 75% (69-81) for the whole series, with no significant differences according to treatment sub-groups. 10-year OS for patients who progressed within 24 months (POD24T) was 60%, in comparison with 85% for patients without progression. Thus the benefit of rituximab maintenance after ASCT on relapse prevention is sustained at 12 years, suggesting that RM adds to ASCT-mediated disease eradication and may enhance the curative potential of ASCT.
AB - We report the 12-year follow-up of the prospective randomized EBMT LYM1 trial to determine whether the benefit of brief duration rituximab maintenance (RM) on progression-free survival (PFS) in patients with relapsed follicular lymphoma (FL) receiving an autologous stem cell transplant (ASCT) is sustained. One hundred and thirty-eight patients received RM with or without purging. The median follow-up after random assignment is 12 years (range 10-13) for the whole series. The 10-year PFS after ASCT is 47% (95% CI 40-54) with only 4 patients relapsing after 7.5 years. RM continues to significantly improve 10-year PFS after ASCT in comparison with NM [P = 0.002; HR 0.548 (95% CI 0.38-0.80)]. Ten-year non-relapse mortality (NRM) was not significantly different between treatment groups (7% overall). 10-year overall survival (OS) after ASCT was 75% (69-81) for the whole series, with no significant differences according to treatment sub-groups. 10-year OS for patients who progressed within 24 months (POD24T) was 60%, in comparison with 85% for patients without progression. Thus the benefit of rituximab maintenance after ASCT on relapse prevention is sustained at 12 years, suggesting that RM adds to ASCT-mediated disease eradication and may enhance the curative potential of ASCT.
KW - Antineoplastic Combined Chemotherapy Protocols
KW - Autografts
KW - Combined Modality Therapy
KW - Follow-Up Studies
KW - Hematopoietic Stem Cell Transplantation
KW - Humans
KW - Lymphoma, Follicular/drug therapy
KW - Neoplasm Recurrence, Local
KW - Prospective Studies
KW - Retrospective Studies
KW - Rituximab/therapeutic use
KW - Transplantation, Autologous
UR - http://www.scopus.com/inward/record.url?scp=85100026005&partnerID=8YFLogxK
U2 - 10.1038/s41409-020-01182-w
DO - 10.1038/s41409-020-01182-w
M3 - Journal article
C2 - 33452448
SN - 0268-3369
VL - 56
SP - 1413
EP - 1421
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 6
ER -