Predictive value of 1q21 gain in multiple myeloma is strongly dependent on concurrent cytogenetic abnormalities and first-line treatment

Improved therapies in multiple myeloma (MM) have forced a constant risk stratification update, first Durie-Salmon, then international scoring systems (ISS), next revised-ISS (RISS) including high-risk cytogenetic abnormalities (HRCAs) such as del(17p) and t(4;14), and now R2-ISS including 1q21 gain...

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Veröffentlicht in:American journal of cancer research 2021-01, Vol.11 (9), p.4438-4454
Hauptverfasser: Minguela, Alfredo, Vasco-Mogorrón, María A, Campillo, José A, Cabañas, Valentin, Remigia, María J, Berenguer, Mercedes, García-Garay, María C, Blanquer, Miguel, Cava, Catalina, Galian, José Antonio, Gimeno, Lourdes, Soto-Ramírez, María F, Martínez-Hernández, María D, de la Rubia, Javier, Teruel, Ana I, Muro, Manuel, Periago, Adela
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Sprache:eng
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Zusammenfassung:Improved therapies in multiple myeloma (MM) have forced a constant risk stratification update, first Durie-Salmon, then international scoring systems (ISS), next revised-ISS (RISS) including high-risk cytogenetic abnormalities (HRCAs) such as del(17p) and t(4;14), and now R2-ISS including 1q21 gain has been proposed. Predictive value of 1q21 gain by itself or in concurrence with other cytogenetic abnormalities is evaluated in 737 real-world plasma cell neoplasm (PCN) patients under current therapies. Ten-year progression-free survival (10y-PFS) rates for patients with 2, 3 and >3 copies of 1q21 were 72.2%, 42.5% and 43.4% (P
ISSN:2156-6976
2156-6976