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Epstein-Peterson, Zachary D; Drill, Esther; Aypar, Umut; Batlevi, Connie Lee; Caron, Philip; Dogan, Ahmet; Drullinsky, Pamela; Gerecitano, John; Hamlin, Paul A; Ho, Caleb; Jacob, Allison; Joseph, Ashlee; Laraque, Leana; Matasar, Matthew J; Moskowitz, Alison J; Moskowitz, Craig H; Mullins, Chelsea; Owens, Colette; Salles, Gilles; Schöder, Heiko; Straus, David J; Younes, Anas; Zelenetz, Andrew D; Kumar, Anita
Haematologica, 04/2024, Volume: 109, Issue: 4Journal Article
Chemoimmunotherapy followed by consolidative high-dose therapy with autologous stem cell rescue was a standard upfront treatment for fit patients with mantle cell lymphoma (MCL) in first remission; however, treatment paradigms are evolving in the era of novel therapies. Lenalidomide is an immunomodulatory agent with known efficacy in treating MCL. We conducted a single-center, investigator-initiated, phase II study of immunochemotherapy incorporating lenalidomide, without autologous stem cell transplant consolidation, enriching for patients with high-risk MCL (clinicaltrials gov. Identifier: NCT02633137). Patients received four cycles of lenalidomide-R-CHOP, two cycles of R-HiDAC, and six cycles of R-lenalidomide. The primary endpoint was rate of 3-year progression-free survival. We measured measurable residual disease (MRD) using a next-generation sequencing-based assay after each phase of treatment and at 6 months following end-oftreatment. We enrolled 49 patients of which 47 were response evaluable. By intent-to-treat, rates of overall and complete response were equivalent at 88% (43/49), one patient with stable disease, and two patients had disease progression during study; 3-year progression-free survival was 63% (primary endpoint not met) and differed by TP53 status (78% wild-type vs. 38% ALT; P=0.043). MRD status was prognostic and predicted long-term outcomes following R-HiDAC and at 6 months following end-of-treatment. In a high-dose therapy-sparing, intensive approach, we achieved favorable outcomes in TP53- wild-type MCL, including high-risk cases. We confirmed that sequential MRD assessment is a powerful prognostic tool in patients with MCL.
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