Publications

Comprehensive analysis of prognostic factors in myelodysplastic syndromes with isolated deletion of chromosome 5q

Montoro MJ, Navarro V, Acha P, Haferlach C, Chan O, Kubota Y, Schulz FI, Briski R, Al-Ali N, Xicoy B, Lopez-Cadenas F, Bosch F, Aguilera A, Meggendorfer M, Eder LN, Jerez A, Wang YH, Campagna A, Lanino L, Betz B, Santini V, Bernal Del Castillo T, Such E, Platzbecker AS, Kewan T, Gurnari C, Zindel C, Kulasekararaj AG, Voso MT, Sekeres MA, Venugopal S, Diaz Varela N, Al-Kali A, Platzbecker U, Haase DT, Zeidan AM, Fenaux P, Díez-Campelo M, Garcia-Manero G, Wiseman DH, Della Porta MG, Germing U, Maciejewski JP, Komrokji RS, Sole F, Haferlach T, Palomo L, Valcarcel D.

Blood Adv

Myelodysplastic syndromes with isolated deletion of chromosome 5q [MDS-del(5q)] constitute a distinct biological entity traditionally associated with favorable outcomes, although up to one quarter of patients progress to acute myeloid leukemia (AML). Existing prognostic models, developed in heterogeneous MDS populations, may not adequately capture risk within this subgroup. We assembled an international cohort of 682 patients with MDS-del(5q) to evaluate the performance of the IPSS-R and IPSS-M, identify prognostic variables, and develop a disease-specific prognostic tool, the IPSS-del(5q). Most patients were classified as lower-risk by IPSS-R (94.4%) and IPSS-M (85.5%), yet both systems showed limited discriminatory ability (C-indices ≈0.5). Independent adverse prognostic factors included age ≥70 years, male sex, anemia (hemoglobin ≤10 g/dL), thrombocytopenia (platelets ≤100×10⁹/L), the presence of one additional chromosomal abnormality, ≥2 gene mutations, SF3B1 mutations, and high-risk TP53 status. Six variables were included in the IPSS-del(5q), stratifying patients into standard-risk (74.3%) and high-risk (25.7%) groups with significantly different LFS (69.2 vs. 32.0 months; p<0.01). Moreover, this model reclassified 19.1% of lower-risk IPSS-R and 14.6% of lower-risk IPSS-M patients into the high-risk IPSS-del(5q) group. However, its discriminative power remained modest, with a C-index of 0.60. Overall, this study provides the most comprehensive prognostic evaluation of MDS-del(5q) to date, demonstrates the limited discriminatory capacity of existing MDS scores in this entity, and underscores the need to develop refined disease-specific prognostic approaches for this MDS subtype.

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