<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ragon BK</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>2746-2757</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10275699</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(12)</volume><pubmed_abstract>The overall survival (OS) has improved significantly in multiple myeloma (MM) over the last decade with the use of proteasome inhibitor and immunomodulatory drug-based combinations, followed by high-dose melphalan and autologous hematopoietic stem cell transplantation (auto-HSCT) and subsequent maintenance therapies in eligible newly diagnosed patients. However, clinical trials using auto-HSCT followed by lenalidomide maintenance have shown an increased risk of second primary malignancies (SPM), including second hematological malignancies (SHM). We evaluated the impact of SPM and SHM on progression-free survival (PFS) and OS in patients with MM after auto-HSCT using CIBMTR registry data. Adult patients with MM who underwent first auto-HSCT in the United States with melphalan conditioning r</pubmed_abstract><journal>Blood advances</journal><pubmed_title>Impact of second primary malignancy post-autologous transplantation on outcomes of multiple myeloma: a CIBMTR analysis.</pubmed_title><pmcid>PMC10275699</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>U24 CA076518</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>P50 CA186781</funding_grant_id><pubmed_authors>Qazilbash MH</pubmed_authors><pubmed_authors>Munshi PN</pubmed_authors><pubmed_authors>Shah N</pubmed_authors><pubmed_authors>Hashmi S</pubmed_authors><pubmed_authors>Nieto Y</pubmed_authors><pubmed_authors>D'Souza A</pubmed_authors><pubmed_authors>Vesole DH</pubmed_authors><pubmed_authors>Mian H</pubmed_authors><pubmed_authors>Badawy SM</pubmed_authors><pubmed_authors>Al Hadidi S</pubmed_authors><pubmed_authors>Shah MV</pubmed_authors><pubmed_authors>George G</pubmed_authors><pubmed_authors>Miller KC</pubmed_authors><pubmed_authors>Kharfan-Dabaja MA</pubmed_authors><pubmed_authors>Battiwalla M</pubmed_authors><pubmed_authors>Saad A</pubmed_authors><pubmed_authors>Solh M</pubmed_authors><pubmed_authors>Nishihori T</pubmed_authors><pubmed_authors>Estrada-Merly N</pubmed_authors><pubmed_authors>Gowda L</pubmed_authors><pubmed_authors>Murthy HS</pubmed_authors><pubmed_authors>Kumar SK</pubmed_authors><pubmed_authors>de Lima M</pubmed_authors><pubmed_authors>Majhail NS</pubmed_authors><pubmed_authors>Patel SS</pubmed_authors><pubmed_authors>Ragon BK</pubmed_authors><pubmed_authors>Afrough A</pubmed_authors><pubmed_authors>Banerjee R</pubmed_authors><pubmed_authors>Lekakis LJ</pubmed_authors><pubmed_authors>Aljurf M</pubmed_authors><pubmed_authors>Hildebrandt GC</pubmed_authors><pubmed_authors>Strouse C</pubmed_authors><pubmed_authors>Pawarode A</pubmed_authors><pubmed_authors>Holmberg LA</pubmed_authors><pubmed_authors>Anderson LD</pubmed_authors><pubmed_authors>Usmani SZ</pubmed_authors><pubmed_authors>Kaur G</pubmed_authors><pubmed_authors>Lee CH</pubmed_authors><pubmed_authors>Abid MB</pubmed_authors><pubmed_authors>Dholaria B</pubmed_authors><pubmed_authors>Gergis U</pubmed_authors><pubmed_authors>Wirk B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of second primary malignancy post-autologous transplantation on outcomes of multiple myeloma: a CIBMTR analysis.</name><description>The overall survival (OS) has improved significantly in multiple myeloma (MM) over the last decade with the use of proteasome inhibitor and immunomodulatory drug-based combinations, followed by high-dose melphalan and autologous hematopoietic stem cell transplantation (auto-HSCT) and subsequent maintenance therapies in eligible newly diagnosed patients. However, clinical trials using auto-HSCT followed by lenalidomide maintenance have shown an increased risk of second primary malignancies (SPM), including second hematological malignancies (SHM). We evaluated the impact of SPM and SHM on progression-free survival (PFS) and OS in patients with MM after auto-HSCT using CIBMTR registry data. Adult patients with MM who underwent first auto-HSCT in the United States with melphalan conditioning r</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-07-14T21:54:28.327Z</modification><creation>2024-12-04T07:31:50.98Z</creation></dates><accession>S-EPMC10275699</accession><cross_references><pubmed>36827681</pubmed><doi>10.1182/bloodadvances.2022009138</doi></cross_references></HashMap>