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Impact of Ultra High-risk Genetics on Real-world Outcomes of Transplant-eligible Multiple Myeloma Patients.
Panopoulou, Aikaterini; Easdale, Sandra; Ethell, Mark; Nicholson, Emma; Potter, Mike; Giotas, Asterios; Woods, Helena; Thornton, Tracy; Pawlyn, Charlotte; Boyd, Kevin D; Kaiser, Martin F.
Afiliação
  • Panopoulou A; Myeloma Molecular Therapy Group, Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
  • Easdale S; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Ethell M; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Nicholson E; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Potter M; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Giotas A; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Woods H; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Thornton T; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Pawlyn C; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
  • Boyd KD; Myeloma Molecular Therapy Group, Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
  • Kaiser MF; Department of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Hemasphere ; 7(2): e831, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36751511
ABSTRACT
Refined prediction of early relapse following standard-of-care (SoC) autologous stem cell transplant (ASCT) in newly diagnosed multiple myeloma (NDMM) could inform real-world risk-stratified post-ASCT strategies. We investigated the impact of double hit genetics (≥2 adverse markers t(4;14), t(14;16), t(14;20), gain(1q), del(17p)) on outcome in 139 NDMM patients who underwent SoC ASCT between January 2014 and October 2019 at our center. Double hit genetics were associated with a significantly shortened progression-free survival (hazard ratio [HR] = 4.27, P < 0.001) and overall survival (HR = 4.01, P = 0.03), and characterized most early relapses. Our results support the real-world utility of extended genetic profiling for improved risk prediction in NDMM.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Hemasphere Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Hemasphere Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido