Interim PET after 4 Cycles Predicts Outcome in Histomolecularly Confirmed Primary Mediastinal B-Cell Lymphoma

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Camus, Vincent | Molina, Thierry | Desmots-Loyer, Fabienne | Blanc-Durand, Paul | Kanoun, Salim | Moslemi, Amine | Ruminy, Philippe | Le Gouill, Steven | Ghesquières, Hervé | Obéric, Lucie | Morschhauser, Franck | Tilly, Hervé | Ribrag, Vincent | Houot, Roch | Thieblemont, Catherine | Maisonneuve, Herve Gerard | Claves, Fabien | Bouabdallah, Krimo | Haioun, Corinne | Damaj, Gandhi Laurent | Fornecker, Luc-Mathieu | Noel, Robin | Feugier, Pierre | Sibon, David | Cartron, Guillaume | Bonnet, Christophe | Bernard, Wivine | Kraeber-Bodéré, Françoise | Bodet-Milin, Caroline | Jais, Jean-Philippe | Brière, Josette | Rossi, Cédric | Elsensohn, Mad-Hélénie | Chartier, Loic | Itti, Emmanuel | Jardin, Fabrice | Fest, Thierry

Edité par CCSD ; The American Society of Hematology -

International audience. The GAINED study (NCT01659099) was a randomized phase 3 trial comparing obinutuzumab (G) to rituximab (R) plus ACVBP or CHOP14 induction, followed by PET-guided consolidation. This post-hoc analysis aimed to detail the outcomes of primary mediastinal B-cell lymphoma (PMBL) patients, verified through expert pathological review and the use of gene-expression profiling (GEP) and Next-Generation sequencing. Of the centrally reviewed 620 patients, 138 (22.3%) confirmed PMBL cases were analyzed. Baseline characteristics included a median age of 33.5 years, 63.8% female, 55.1% stage III-IV, 90.6% elevated LDH, 87.6% ECOG 0-1, 62.3% extranodal involvement, 52.6% aaIPI 2-3, and 53.6% Bulk (>10cm). Induction regimens were R/G-CHOP14 (56.9%) and R/G-ACVBP (43.1%). Post-induction treatments, based on interim PET (iPET) results, included: standard consolidation chemotherapy (59.8%) if ΔSUVmax >66% after cycle 2 and >70% after cycle 4 (PET2−/4−), intensive treatment and autologous transplantation (26.8%) if PET2+/4-, and salvage therapy (13.4%) if PET4+ (ΔSUVmax ≤70%). Among patients with GEP data (n=107), 38 (35.5%) were PDL1high/PDL2high. Key somatic mutations data (n=87) included SOCS1 (70.1%), B2M (56.3%), STAT6 (49.4%), TNFAIP3 (47.1%), GNA13 (39.1%), CIITA (37.9%), CD58 (36.8%), and TP53 (29.9%). After a median follow-up of 39.5 months, 2-year PFS and OS rates were 86.2% and 93.2%, respectively. In a multivariate model including Bulk, aaIPI, and ΔSUVmax PET2/PET4, only Bulk and ΔSUVmax PET4 ≤70% were associated with shorter PFS (HR 4.39 [1.28-15.11] and 4.95 [1.71-14.3], respectively), while none were associated with OS. The ΔSUVmax-based interim PET4 response emerged as the strongest predictor of patient outcomes in this selected clinical trial population.Clinical trial registration information (if any): NCT01659099

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