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An early post-transplant relapse prediction score in multiple myeloma: a large cohort study from the chronic malignancies working party of EBMT. | LitMetric

AI Article Synopsis

  • Early relapse (ER) after Autologous Hematopoietic Cell Transplantation (AHCT) is linked to a poor prognosis, prompting the development of a new scoring system to predict ER risk.
  • The study analyzed data from 14,367 AHCT patients, revealing distinct probabilities for progression-free survival (PFS-12) and relapse incidence, which varied based on treatment regimens (Melphalan 200 mg/m vs. Melphalan 140).
  • The scoring system categorizes patients based on their International Staging System (ISS) stages, disease status, and performance status, leading to five risk groups that can significantly predict the likelihood of relapse and inform patient management strategies.

Article Abstract

Early relapse (ER) following Autologous Hematopoietic Cell Transplantation (AHCT) confers a poor prognosis. We therefore developed a novel scoring system to predict ER. A total of 14,367 AHCT-1 patients were transplanted between 2014 and 2019, and were conditioned with Melphalan 200 mg/m (Mel200) (n = 7228; 2014-2017) (training cohort); Mel200 (n = 5616; 2018-2019) or Mel140 (n = 1523; 2018-2019) (validation cohorts). PFS-12 and the Cumulative Incidence of Relapse at 12 months were 84.1% and 14.7% (training Mel200), 87.2% and 11.6% (validation Mel200), and 80.3% and 16.9% (validation Mel140), respectively. The points in the risk score were: 0, 1,2 for ISS stages I, II, and III; Disease status: 0 (CR/VGPR); 1 (PR); 2 (SD/MR); 4 (Relapse/Progression); and 1 for Karnofsky ≤ 70. The distribution of scores: 0 (24%), 1 (33.9%), 2 (29.6 %), 3 (9.5%), and ≥4 (2.7%). The score separated PFS-12, with the lowest risk group (n = 1752) having a PFS-12 of 91.7% and the highest risk group (n = 195) 57.1%. This also applied in cytogenetically high-risk patients. If the pre-score baseline risks are 15% (standard risk) and 25% (high-risk), a score of ≥4 confers calculated risks of 38% and 54%, respectively. This novel EBMT ER score, therefore, allows for the identification of five discrete prognostic groups.

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Source
http://dx.doi.org/10.1038/s41409-023-01999-1DOI Listing

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