Adjuvant rituximab and elevated intratumoural CD8 expression are associated with sustained disease control after radiotherapy in early-stage follicular lymphoma: TROG99.03

Author:

MacManus Michael P.,Seymour John F,Tsang Hennes,Fisher Richard,Keane Colm,Sabdia Muhammed B,Law Soi C,Gunawardana Jay,Nath Karthik,Kazakoff Stephen H,Marques-Piubelli Mario L,Duenas Daniela E,Green Michael R,Roos Daniel,O’Brien Peter,McCann Andrew,Tsang Richard,Davis Sidney,Christie David,Cheah Chan,Amanuel Benhur,Cochrane Tara,Butler Jason,Johnston Anna,Shanavas Mohamed,Li Li,Vajdic Claire,Kridel Robert,Shelton Victoria,Hershenfield Samantha,Baetz Tara,Lebrun David,Johnson Nathalie,Brodtkorb Marianne,Ludvigsen Maja,d’Amore Francesco,Thompson Ella R,Blombery Piers,Gandhi Maher K,Tobin Joshua WD

Abstract

AbstractBackgroundWe report extended follow-up of TROG99.03, a randomised phase III trial in early-stage follicular lymphoma (ESFL) including new information on the role of adjuvant rituximab and translational studies.MethodsPatients with ESFL were randomised to involved-field radiotherapy (IFRT) or IFRT plus 6-cycles cyclophosphamide/vincristine/prednisolone (IFRT+CVP). From 2006 rituximab was added to IFRT+CVP (IFRT+R-CVP). Clinical and multi-omic parameters were evaluated. Findings were validated in two independent ESFL cohorts (99 and 60 patients respectively).FindingsBetween 2000-2012, 150 (75 per arm) patients were recruited. 48% were positron emission tomography (PET)-staged. Per protocol, at median follow-up 11.3-years, progression-free survival (PFS) remained superior for IFRT+(R)CVP vs. IFRT (hazard ratio [HR]=0.60, 95%CI=0.37-0.98, p=0.043; 10-year PFS 62% vs. 43%) respectively. Although no significant difference in overall survival was observed (HR=0.44, 95%CI=0.16-1.18, p=0.11, 10-year OS 95% vs 84%), patients receiving IFRT+(R)CVP experienced fewer composite (histological transformation and death) events (p=0.045). PFS of IFRT+R-CVP-treated patients compared with all other treatments lacking rituximab (IFRT alone plus IFRT+CVP) was superior (HR=0.36, 95%CI=0.13-0.82, p=0.013). Amongst PET-staged patients, PFS differences between IFRT+R-CVP vs. IFRT were maintained (HR=0.38, 95%CI=0.16-0.89, p=0.027) indicating benefit distinct from stage migration. FL-related mutations andBCL2-translocations were not associated with PFS. However, by multivariate analysis elevated CD8A gene expression in diagnostic biopsy tissue was independently associated with improved PFS (HR=0.45, 95%CI=0.26-0.79, p=0.037), a finding confirmed in both ESFL validation cohorts. CD8A gene expression was raised (p=0.02) and CD8+ T-cell density higher within follicles in ESFL vs. advanced-stage FL (p=0.047). Human leucocyte antigen class I specific neoantigens were detected in 43% of patients, suggesting neoantigen-specific CD8+ T-cells have a role in confining the spread of the disease.InterpretationAdjuvant R-CVP and elevated intratumoural CD8 expression were independently associated with sustained disease control after radiotherapy in ESFL.FundingCancer Council Victora; National Health and Medical Research Council; Leukaemia Foundation; Mater Foundation.

Publisher

Cold Spring Harbor Laboratory

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