Evidence map›Paper›PMID 42379751›Full record

ArticleIn vivo (Athens, Greece)

Outcomes of Supplementation With β-Hydroxy-β-methylbutyrate, Arginine, and Glutamine During Carbon-ion Radiotherapy for Head and Neck Cancer: A Prospective Exploratory Study.

Atsushi Musha, Nobuteru Kubo, Masahiro Onishi, Takeru Ohtaka, Tatsuya Ohno

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Article in In vivo (Athens, Greece). 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Atsushi MushaGunma University Heavy Ion Medical Center, Maebashi, Gunma, Japan; musha@gunma-u.ac.jp.
Nobuteru KuboGunma University Heavy Ion Medical Center, Maebashi, Gunma, Japan.
Masahiro OnishiGunma University Heavy Ion Medical Center, Maebashi, Gunma, Japan.
Takeru OhtakaGunma University Heavy Ion Medical Center, Maebashi, Gunma, Japan.
Tatsuya OhnoGunma University Heavy Ion Medical Center, Maebashi, Gunma, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAcute mucositis and dermatitis frequently occur during radiotherapy for head and neck malignancies and can impair oral intake and quality of life (QOL). Nutritional supplementation using β-hydroxy-β-methylbutyrate (HMB), arginine (Arg), and glutamine (Gln) may support tissue repair and protein metabolism. This prospective single-arm exploratory study evaluated the feasibility of continuous oral HMB-Arg-Gln supplementation during carbon-ion radiotherapy (CIRT). PATIENTS AND

methodsSixteen consecutive patients with head and neck tumors who underwent CIRT were enrolled. Patients received oral HMB-Arg-Gln supplementation twice daily from the start of CIRT until 2 weeks after treatment completion. The primary endpoint was feasibility, defined as completion of CIRT with continuous supplementation without grade ≥4 acute toxicity or the need for enteral or parenteral nutritional support. Acute mucositis and radiation dermatitis were graded weekly using Common Terminology Criteria for Adverse Events v4.03 and Radiation Therapy Oncology Group criteria. Health-related QOL was assessed using Short Form-8 (SF-8) questionnaires before CIRT, at completion of 16 fractions, and 2 months after treatment.

resultsAll patients completed the CIRT course with supplementation, meeting the predefined feasibility criteria. No grade ≥4 acute toxicities occurred. Temporal mucositis and dermatitis patterns were consistent with those typically reported during radiotherapy, with peak severity near the end of treatment. SF-8 physical component summary scores had decreased at CIRT completion but had partially recovered by 2 months, whereas mental component summary scores remained relatively stable.

conclusionContinuous oral HMB-Arg-Gln supplementation during CIRT for head and neck tumors was feasible and well tolerated. Treatment was completed without severe acute toxicity, and QOL was largely maintained during and after therapy. Nutritional supplementation may support patients undergoing particle therapy.

Indexed as

ArginineDietary SupplementsGlutamineHead and Neck NeoplasmsHeavy Ion RadiotherapyValeratesAdultAgedFemaleHumansMaleMiddle AgedMucositisProspective StudiesQuality of LifeTreatment OutcomeArgininebeta-hydroxyisovaleric acidGlutamineValeratescarbon-ion radiotherapydermatitisHead and neck cancermucositisquality of life

Identifiers

PMID42379751
PMCPMC13322110

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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.