IgD Subtype But Not IgM or Non-Secretory Is a Prognostic Marker for Poor Survival Following Autologous Hematopoietic Cell Transplantation in Multiple Myeloma. Results From the EBMT CALM (Collaboration to Collect Autologous Transplant Outcomes in Lymphomas and Myeloma) Study
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
34158265
DOI
10.1016/j.clml.2021.05.012
PII: S2152-2650(21)00199-3
Knihovny.cz E-zdroje
- Klíčová slova
- IgD myeloma, Oligosecretory myeloma, Overall survival, Plerixafor, Progression free survival,
- MeSH
- analýza přežití MeSH
- autologní transplantace metody mortalita MeSH
- doba přežití bez progrese choroby MeSH
- dospělí MeSH
- imunoglobulin D metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mnohočetný myelom MeSH
- příprava pacienta k transplantaci metody mortalita MeSH
- senioři MeSH
- transplantace hematopoetických kmenových buněk metody mortalita MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- imunoglobulin D MeSH
BACKGROUND: The Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study has provided an opportunity to evaluate the real-world outcomes of patients with myeloma. The aim of this study was to compare the outcome according to the different subtypes of myeloma using CALM data. PATIENTS: This study compared overall survival (OS), progression-free survival (PFS), and complete remission (CR) and the impact of novel versus non-novel drug containing induction regimens prior to autologous hematopoietic cell transplantation (HCT) of 2802 patients with "usual" and "rare" myelomas. RESULTS: Our data suggest that IgM and non-secretory myeloma have superior PFS and OS compared with IgD myeloma and outcomes comparable to those for usual myeloma. Patients who received novel agent induction had higher rates of CR prior to transplant. Non-novel induction regimens were associated with inferior PFS but no difference in OS. Although not the primary focus of this study, we show that poor mobilization status is associated with reduced PFS and OS, but these differences disappear in multivariate analysis suggesting that poor mobilization status is a surrogate for other indicators of poor prognosis. CONCLUSION: We confirm that IgD myeloma is associated with the worst prognosis and inferior outcomes compared with the other isotypes.
Azienda Ospedaliera Papa Giovanni XXIII Bergamo Italy
Belfast City Hospital Belfast Northern Ireland United Kingdom
Central Clinical Hospital Warsaw Poland
Dél pesti Centrumkórház Budapest Hungary
EBMT Data Office Leiden Leiden Netherlands
George Papanicolaou General Hospital Thessaloniki Greece
Hammersmith Hospital London United Kingdom
Heinrich Heine Universität Düsseldorf Düsseldorf Germany
Hospital Pitié Salpêtrière Paris France
Hospital Universitario Central de Asturias Oviedo Asturias Spain
Institut Paoli Calmettes Marseille France
Karolinska University Hospital Stockholm Sweden
Lille University Hospital Lille France
Nottingham University Nottingham United Kingdom
Queens University of Belfast Belfast Northern Ireland United Kingdom
Radboud University Medical Centre Nijmegen Netherlands
Skanes University Hospital Lund Sweden
St James's Hospital Dublin Ireland
St James's University Hospital of Wales Cardiff Wales United Kingdom
Tor Vergata University of Rome Rome Italy
Umeå University Hospital Umeå Sweden
University Hospital Brno Brno Czech Republic
University Hospital Eppendorf Hamburg Germany
University Hospital Heidelberg Heidelberg Germany
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