| Literature DB >> 34289038 |
Michele Cavo1, Jesus San-Miguel2, Saad Z Usmani3, Katja Weisel4, Meletios A Dimopoulos5, Hervé Avet-Loiseau6, Bruno Paiva2, Nizar J Bahlis7, Torben Plesner8, Vania Hungria9, Philippe Moreau10, Maria-Victoria Mateos11, Aurore Perrot12, Shinsuke Iida13, Thierry Facon14, Shaji Kumar15, Niels W C J van de Donk16, Pieter Sonneveld17, Andrew Spencer18, Maria Krevvata19, Christoph Heuck19, Jianping Wang20, Jon Ukropec21, Rachel Kobos19, Steven Sun20, Mia Qi20, Nikhil Munshi22,23.
Abstract
We explored minimal residual disease (MRD) in relapsed/refractory multiple myeloma (RRMM) and transplant-ineligible (TIE) newly diagnosed multiple myeloma (NDMM) using data from 4 phase 3 studies (POLLUX, CASTOR, ALCYONE, and MAIA). Each study previously demonstrated that daratumumab-based therapies improved MRD negativity rates and reduced the risk of disease progression or death by approximately half vs standards of care. We conducted a large-scale pooled analysis for associations between patients achieving complete response or better (≥CR) with MRD-negative status and progression-free survival (PFS). MRD was assessed via next-generation sequencing (10-5 sensitivity threshold). Patient-level data were pooled from all 4 studies and for patients with TIE NDMM and patients with RRMM who received ≤2 prior lines of therapy (≤2 PL). PFS was evaluated by response and MRD status. Median follow-up (months) was 54.8 for POLLUX, 50.2 for CASTOR, 40.1 for ALCYONE, and 36.4 for MAIA. Patients who achieved ≥CR and MRD negativity had improved PFS vs those who failed to reach CR or were MRD positive (TIE NDMM and RRMM hazard ratio [HR] 0.20, P < .0001; TIE NDMM and RRMM ≤2 PL HR 0.20, P < .0001). This benefit occurred irrespective of therapy or disease setting. A time-varying Cox proportional hazard model confirmed that ≥CR with MRD negativity was associated with improved PFS. Daratumumab-based treatment was associated with more patients reaching ≥CR and MRD negativity. These findings represent the first large-scale analysis with robust methodology to support ≥CR with MRD negativity as a prognostic factor for PFS in RRMM and TIE NDMM. These trials were registered at www.clinicaltrials.gov as #NCT02076009, #NCT02136134, #NCT02195479, and #NCT02252172.Entities:
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Year: 2022 PMID: 34289038 PMCID: PMC8832474 DOI: 10.1182/blood.2021011101
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476