PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 5, 2026Cancer Research0 citations

Abstract 4624: Investigation of the efficacy of reduced coenzyme Q10 (CoQ10) for alleviating acute intestinal toxicity associated with pelvic radiotherapy: A randomized, placebo-controlled, double-blind comparative study

View Full Paper
SSSatoshi SenoAKA. KajiwaraYSYASUYUKI SHIMIZU

Key Points

  • This study aims to evaluate the effectiveness of reduced coenzyme Q10 in mitigating diarrhea caused by pelvic radiotherapy.
  • Randomized, placebo-controlled clinical study
  • Included patients with cervical, endometrial, or vaginal cancer undergoing radiotherapy
  • Participants received 200 mg rCoQ10 or placebo daily before and during radiotherapy
  • Adverse events graded using CTCAE version 5.0
  • Median maximum increase in bowel movements: 5.3 in rCoQ10 group vs. 5.8 in placebo group (p = 0.937)
  • No significant difference in overall diarrhea incidence or severity
  • Trend towards reduced Grade 2 diarrhea occurrence in rCoQ10 group
  • 2-year progression-free survival: 80.4% for rCoQ10 vs. 84.0% for placebo (p = 0.491)

Abstract

Abstract Background: Diarrhea is one of the major acute adverse effects in patients undergoing pelvic radiotherapy, often impairing treatment continuity and quality of life. Despite its clinical importance, the pathogenesis of radiation-induced diarrhea (RID) remains inadequately understood, and effective prophylactic strategies have yet to be established. Reduced coenzyme Q10 (rCoQ10) possesses antioxidant properties capable of neutralizing activated reactive oxygen species generated during irradiation. This study aimed to evaluate whether oral administration of rCoQ10 could mitigate intestinal mucosal damage and reduce the severity of diarrhea in patients receiving curative pelvic radiotherapy. Materials and Methods: This randomized, placebo-controlled clinical study included patients with cervical, endometrial, or vaginal cancer (FIGO 2018 Stage IB-IVA) treated with radiotherapy at Kobe University Hospital between June 2021 and November 2023. Eligible patients were ≥20 years old, had ECOG Performance Status 0-2, and provided written informed consent. A total of 47 patients were randomized into rCoQ10 and placebo groups. Participants received three 200 mg soft capsules of rCoQ10 or placebo orally once daily starting 5-7 days before radiotherapy. From the first day of radiotherapy, capsules were taken once daily approximately one hour before each irradiation session. Thirty patients (63.8%) underwent IMRT, and 33 patients (70.2%) received concurrent chemotherapy with weekly cisplatin (40 mg/m2). Adverse events, including diarrhea, were graded according to CTCAE version 5.0. The primary endpoint was the maximum increase in the number of daily bowel movements during the radiotherapy period. Analyses were adjusted for chemotherapy use and radiotherapy modality. Results: Among the 47 enrolled patients, 44 were evaluable for analysis (two withdrew consent and one discontinued due to cognitive decline). The median maximum increase in bowel movements was 5.3 in the rCoQ10 group and 5.8 in the placebo group, showing no significant difference (p = 0.937). While the overall incidence and severity distribution of diarrhea did not significantly differ, a trend toward reduced occurrence of Grade 2 diarrhea was observed in the rCoQ10 group. The 2-year progression-free survival was 80.4% in the rCoQ10 group and 84.0% in the placebo group (p = 0.491), indicating no negative influence on oncologic treatment efficacy. No serious adverse events related to rCoQ10 were reported. Conclusions: Although the primary endpoint was not met, rCoQ10 showed a potential benefit in reducing moderate diarrhea in patients undergoing pelvic radiotherapy, without compromising cancer treatment outcomes. Further large-scale studies are warranted to clarify its clinical utility as a supportive therapy. Citation Format: Satoshi Seno, Akifumi Kajiwara, Yasuyuki Shimizu, Kazuma Iwashita, Kana Kobayashi, Qin Qin, Qu Zhang, Hatamei Takabayashi, Kanako Suda, Hiroki Kawaguchi, Takeaki Ishihara, Daisuke Miyawaki, Sae Murakami, Yoshito Terai, Ryohei Sasaki. Investigation of the efficacy of reduced coenzyme Q10 (CoQ10) for alleviating acute intestinal toxicity associated with pelvic radiotherapy: A randomized, placebo-controlled, double-blind comparative study abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4624.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Seno et al. (2026) studied this question.

synapsesocial.com/papers/69d1fde4a79560c99a0a443dhttps://doi.org/10.1158/1538-7445.am2026-4624
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Coenzyme Q10 as an adjunctive strategy to reduce paclitaxel-induced toxicities in breast cancer: a randomized controlled trial2026
  2. 2Efficacy of Coenzyme Q10 for Improved Tolerability of Cancer Treatments: A Systematic Review2004 · 79 citations
  3. 3Phase I Randomized, Placebo-Controlled, Cross-Over Dose-Finding Study of Coenzyme Q10 on Doxorubicin Pharmacokinetics during Breast Cancer Treatment2025 · 3 citations
  4. 4Protective effects of coenzyme Q10 against cyclophosphamide induced ovarian damage in rats2025
  5. 5Protective effects of coenzyme Q10 against cyclophosphamide induced ovarian damage in rats2025 · 1 citations