Evidence map›Paper›PMID 39985640›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2025

Incidence of engraftment syndrome with and without budesonide prophylaxis in patients with multiple myeloma undergoing autologous stem cell transplant.

Lucy Gloe, Alexandria Rakestraw, Stephanie Daniels, Xianyan Chen, Vamsi Kota, Amber B Clemmons

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Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Lucy GloeWellstar MCG Health and University of Georgia College of Pharmacy, Augusta, GA, 30912, USA.
Alexandria RakestrawUniversity of Georgia College of Pharmacy, Augusta, GA, 30912, USA.
Stephanie DanielsBone Marrow Transplant/Cellular Therapy Program, Wellstar MCG Health and the Georgia Cancer Center, Augusta, GA, 30912, USA.
Xianyan ChenDepartment of Epidemiology & Biostatistics, University of Georgia (UGA), Athens, GA, USA.
Vamsi KotaWellstar MCG Health and the Georgia Cancer Center, Augusta, GA, 30912, USA.
Amber B ClemmonsUniversity of Georgia College of Pharmacy and Wellstar MCG Health, 914 New Bailie Street, HM Building, Room 104, Augusta, GA, 30912, USA. aclemmons@augusta.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEngraftment syndrome (ES), a rare post-transplant complication, has been defined differently across the literature. This study aims to determine if budesonide prophylaxis reduces ES after autologous hematopoietic cell transplantation (auto-HCT) for patients with multiple myeloma (MM), as defined by the published Spitzer or Maiolino criteria or by the ES definition used by Dhakal et al.

methodsA single-center retrospective review was conducted on adult patients who received auto-HCT for MM between January 2017 and October 2023. Patients were divided into those who did not receive budesonide prophylaxis (n = 169) versus those who did (n = 144). The primary endpoint was an incidence of ES by the definition used by Spitzer, Maiolino, and Dhakal et al., respectively. Secondary endpoints included receipt of steroids to treat ES, hospital length of stay, engraftment, and 30- and 100-day mortality rates. Exploratory endpoints were antibiotics started in the peri-engraftment period and number of anti-diarrheal and anti-emetic doses.

resultsNo difference existed between groups in the primary outcome by the ES definition used by Spitzer, Maiolino, or Dhakal et al. (all p > 0.05). Further, no difference existed with respect to any secondary outcomes (all p > 0.05) except a lower incidence of receipt of antibiotics in the peri-engraftment period for those who received budesonide.

conclusionOur findings suggest concordance between Spitzer and Maiolino criteria with clinically documented ES, with higher incidences when the ES definition used by Dhakal et al. is utilized. Larger controlled trials need to be performed to validate these findings.

Indexed as

BudesonideGraft vs Host DiseaseHematopoietic Stem Cell TransplantationMultiple MyelomaAdultAgedFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesSyndromeTransplantation, AutologousBudesonideAutologousBudesonideEngraftment syndromeMyelomaTransplant

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.