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- W2155535356 abstract "Abstract Before the introduction of new drugs, we designed a trial where treatment of newly diagnosed myeloma patients was based on the presence or absence of HLA-identical siblings. First-line treatments included a cytoreductive autograft followed by a nonmyeloablative allograft or a second melphalan-based autograft. Here, we report long-term clinical outcomes and discuss them in the light of the recent remarkable advancements in the treatment of myeloma. After a median follow-up of 7 years, median overall survival (OS) was not reached (P = .001) and event-free survival (EFS) was 2.8 years (P = .005) for 80 patients with HLA-identical siblings and 4.25 and 2.4 years for 82 without, respectively. Median OS was not reached (P = .02) and EFS was 39 months (P = .02) in the 58 patients who received a nonmyeloablative allograft whereas OS was 5.3 years and EFS 33 months in the 46 who received 2 high-dose melphalan autografts. Among patients who reached complete remission in these 2 cohorts, 53% and 19% are in continuous complete remission. Among relapsed patients rescued with “new drugs,” median OS from the start of salvage therapy was not reached and was 1.7 (P = .01) years, respectively. Allografting conferred a long-term survival and disease-free advantage over standard autografting in this comparative study." @default.
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- W2155535356 date "2011-06-16" @default.
- W2155535356 modified "2023-10-18" @default.
- W2155535356 title "Long-term follow-up of a comparison of nonmyeloablative allografting with autografting for newly diagnosed myeloma" @default.
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- W2155535356 doi "https://doi.org/10.1182/blood-2011-03-339945" @default.
- W2155535356 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3251223" @default.
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