Title | Long-term survival of 1338 MM patients treated with tandem autologous vs. autologous-allogeneic transplantation. |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Costa, LJ, Iacobelli, S, Pasquini, MC, Modi, R, Giaccone, L, Blade, J, Schonland, S, Evangelista, A, Perez-Simon, JA, Hari, P, Brown, EE, Giralt, SA, Patriarca, F, Stadtmauer, EA, Rosinol, L, Krishnan, AY, Gahrton, G, Bruno, B |
Journal | Bone Marrow Transplant |
Volume | 55 |
Issue | 9 |
Pagination | 1810-1816 |
Date Published | 2020 09 |
ISSN | 1476-5365 |
Keywords | Disease-Free Survival, Graft vs Host Disease, Hematopoietic Stem Cell Transplantation, Humans, Neoplasm Recurrence, Local, Transplantation Conditioning, Transplantation, Autologous, Transplantation, Homologous |
Abstract | Contrary to tandem autologous transplant (auto-auto), autologous followed by reduced intensity conditioning allogenic transplantation (auto-allo) offers graft-versus-myeloma (GVM) effect but with higher toxicity. Trials comparing these two strategies relied on availability of HLA-matched sibling donors for arm allocation (biological randomization) and yielded conflicting results. A pooled analysis of multiple trials with extended follow up provides an opportunity to compare these strategies. We obtained individual patient data from participants of four trials comparing auto-auto vs. auto-allo after induction therapy. There were 899 patients in auto-auto and 439 in auto-allo. Median follow up of survivors was 118.5 months. Median overall survival (OS) was 78.0 months in auto-auto and 98.3 months in auto-allo (HR = 0.84, P = 0.02). OS was 36.4% vs. 44.1% at 10 years (P = 0.01) for auto-auto and auto-allo, respectively. Progression-free survival was also improved in auto-allo (HR = 0.84, P = 0.004). Risk of non-relapse mortality was higher in auto-allo (10 year 8.3% vs. 19.7%, P |
DOI | 10.1038/s41409-020-0887-4 |
Alternate Journal | Bone Marrow Transplant |
PubMed ID | 32286506 |
PubMed Central ID | PMC7483973 |
Grant List | UG1 HL069286 / HL / NHLBI NIH HHS / United States UG1 HL069278 / HL / NHLBI NIH HHS / United States P30 CA008748 / CA / NCI NIH HHS / United States U01 HL069294 / HL / NHLBI NIH HHS / United States U10 CA180888 / CA / NCI NIH HHS / United States U24 CA076518 / CA / NCI NIH HHS / United States U24 HL138660 / HL / NHLBI NIH HHS / United States |