| Literature DB >> 32034285 |
Hartmut Goldschmidt1,2, Elias K Mai3, Jan Dürig4, Christof Scheid5, Katja C Weisel6,7, Christina Kunz8, Uta Bertsch3,9, Thomas Hielscher8, Maximilian Merz3, Markus Munder10, Hans-Walter Lindemann11, Barbara Hügle-Dörr3, Diana Tichy8, Nicola Giesen3, Dirk Hose3, Anja Seckinger3, Stefanie Huhn3, Steffen Luntz12, Anna Jauch13, Ahmet Elmaagacli14, Bernhard Rabold12, Stephan Fuhrmann15, Peter Brossart16, Martin Goerner17, Helga Bernhard18, Martin Hoffmann19, Jens Hillengass3,20, Marc S Raab3, Igor W Blau21, Mathias Hänel22, Hans J Salwender23.
Abstract
The MM5 trial aimed at demonstrating a progression-free survival (PFS) difference in continued vs. response-adapted (in case of complete response, CR) lenalidomide (LEN) maintenance therapy (MT) in newly diagnosed, transplant-eligible multiple myeloma (MM). Patients were equally randomized to receive induction therapy with PAd (bortezomib/doxorubicin/dexamethasone) or VCD (bortezomib/cyclophosphamide/dexamethasone), high-dose melphalan and autologous blood stem cell transplantation, and LEN consolidation, followed by either LEN MT for a fixed duration of 2 years (LEN-2Y) or until achievement of CR (LEN-CR, intention-to-treat population n = 502): arms A1:PAd + LEN-2Y (n = 125), B1:PAd + LEN-CR (n = 126), A2:VCD + LEN-2Y (n = 126), B2:VCD + LEN-CR (n = 125). In the LEN-CR group (B1 + B2), n = 88/17.5% patients did not start or discontinued LEN MT due to CR. There was no PFS (p = 0.60, primary endpoint) nor overall survival (OS) (p = 0.15) difference between the four study arms. On pooled LEN MT strategies, OS (hazard ratio, hazard ratio [HR] = 1.42, p = 0.03) but not PFS (HR = 1.15, p = 0.20) was shorter in LEN-CR (B1 + B2) vs. LEN-2Y (A1 + A2) groups. PFS was shortened on landmark analyses from the start of LEN MT in patients being in CR in the LEN-CR group (LEN-CR vs. LEN-2Y, HR = 1.84, p = 0.02). OS from first progression was shortened in the LEN-CR vs. LEN-2Y group (HR = 1.60, p = 0.01). LEN MT should be applied beyond CR for at least 2 years.Entities:
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Year: 2020 PMID: 32034285 DOI: 10.1038/s41375-020-0724-1
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528