AI Article Synopsis

  • Malnutrition raises non-relapse mortality risks in patients undergoing allogeneic stem cell transplantation (aHSCT), prompting the ALLONUT trial to assess tailored nutritional support.
  • The trial, involving 70 patients, demonstrated significant nutritional improvement through personalized outpatient nutrition programs and cooking classes, with malnutrition rates dropping from 26.9% at Day 30 to 10.8% one year post-transplant.
  • Quality of life (QoL) initially declined but returned to pre-transplant levels by Day 100 and exceeded those levels by Day 360, highlighting the program's effectiveness in enhancing both nutrition and QoL post-aHSCT.

Article Abstract

Malnutrition increases the risk of non-relapse mortality after allogeneic stem cell transplantation (aHSCT). Here are the results of the ALLONUT clinical trial designed to improve the nutritional outcome of patients receiving aHSCT. ALLONUT is a prospective open label phase 2 clinical trial assessing the efficacy of a close tailored nutritional support and management with traditional and original solutions to improve patients nutritional status following aHSCT. Nutritional status evaluation was performed before transplantation, on Day 0, 30, 100 and one year after transplantation. The study involved 70 patients treated by aHSCT. 10% of patients were moderately or severely malnutrition at baseline and 26.9 were severely malnutrition at D30. Patients' nutritional status improved thanks to the cooking classes and the personalized outpatient nutrition program. At D100, 23% were still malnutrition, while only 10.8% were severely malnutrition one year after transplantation. The QLQ-C30 show that quality of life (QoL) decreased until D30, and improve to reach the pre-transplant level on D100 before exceeding it on D360. The study confirmed that a close, personalized nutritional program combining traditional and original measures can improve both nutritional status and QoL for patients suffering from moderate or severe malnutrition after aHCST.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11226397PMC
http://dx.doi.org/10.1038/s41409-024-02271-wDOI Listing

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