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Impact of maintenance therapy post autologous stem cell transplantation for multiple myeloma in early and delayed transplant. | LitMetric

AI Article Synopsis

  • Maintenance therapy after autologous stem cell transplantation (ASCT) has become standard practice for multiple myeloma, with 39% of patients receiving it, particularly benefiting those who had early ASCT (42%) compared to delayed ASCT (30.5%).
  • The most common maintenance treatments were IMiDs (61%), followed by PIs (31%), with higher use of PI maintenance in high-risk patients.
  • Results showed significantly improved progression-free survival (PFS) and overall survival (OS) for patients on maintenance therapy, with PFS at 36 months versus 22 months and OS at 93 months versus 73 months, affirming phase 3 trial findings in a real-world patient cohort.

Article Abstract

Based on phase 3 trials, maintenance therapy after autologous stem cell transplantation (ASCT) has become the standard of care in multiple myeloma (MM). We examined the trends in maintenance therapy in a large group of patients (2530) transplanted at a single institution over two decades. Majority (n = 1958; 77%) had an ASCT within 12 months of diagnosis (early ASCT). Maintenance was employed in 39% of the patients; 42% among early ASCT and 30.5% among delayed ASCT. Most common maintenance approach was an IMiD (61%), followed by a PI (31%), or a PI + IMiD (4%). Patients with high-risk FISH received PI-based maintenance more frequently. The PFS was superior with maintenance (36 vs. 22 months, p < 0.001); 37 vs. 25 months for early ASCT (p < 0.001) and 29 vs. 17 months for delayed ASCT (p = 0.0008). OS from ASCT was higher with maintenance for the whole cohort at 93 vs. 73 months (p < 0.001). OS from diagnosis was also better for the whole cohort with maintenance therapy, 112 vs. 93 months (p < 0.001). The improvement in PFS and OS was seen in high-risk and standard risk disease. The experience with maintenance therapy post ASCT for myeloma in a non-clinical trial setting confirms the findings from the phase 3 trials.

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Source
http://dx.doi.org/10.1038/s41409-022-01631-8DOI Listing

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