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Therapeutic Effect of Anti-Inflammatory Tripeptide Cream in Hand-Foot Syndrome/Skin Reaction Related to Anticancer Drugs: a Randomized, Double-Blind, Placebo-Controlled Pilot Trial.
Yang, Yaewon; Hahn, Jang-Hee; Kim, Min Seo; Jo, Minkwan; Lee, Yong-Pyo; Kim, Hongsik; Kim, Hee Kyung; Kwon, Jihyun; Lee, Ki Hyeong; Han, Hye Sook.
Affiliation
  • Yang Y; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Hahn JH; Department of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, Korea.
  • Kim MS; Department of Anatomy and Cell Biology, School of Medicine, Kangwon National University, Chuncheon, Korea.
  • Jo M; SupadElixir Co., Ltd., Chuncheon, Korea.
  • Lee YP; SupadElixir Co., Ltd., Chuncheon, Korea.
  • Kim H; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Kim HK; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Kwon J; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Lee KH; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Han HS; Department of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, Korea.
Cancer Res Treat ; 2024 Jun 07.
Article in En | MEDLINE | ID: mdl-38853540
ABSTRACT

Purpose:

Hand-foot syndrome (HFS) and hand-foot skin reaction (HFSR) are relatively common toxicities that interfere with the quality of life (QoL) of patients with cancer. Anti-inflammatory tripeptide cream (ATPC) is a complex formulation of anti-inflammatory tripeptides, the CD99-agonist BinterinTM and the Wnt-antagonist WinhibinTM. The present study aimed to assess the therapeutic effects of ATPC in HFS/HFSR associated with anticancer drugs. Materials and

Methods:

This was a single-center, randomized, double-blind, placebo-controlled trial. Patients who developed grade 1 HFS/HFSR after systemic anticancer treatments were enrolled, and randomly assigned to receive either ATPC or placebo cream (PC) and followed up at 3-week intervals for up to nine weeks. Primary endpoint was the development of grade ≥ 2 HFS/HFSR.

Results:

Between April 2019 and July 2022, 60 patients (31 in the ATPC and 29 in the PC group) completed the study. The incidence of grade ≥ 2 HFS/HFSR was significantly lower in the ATPC than in the PC group (25.8% vs. 51.7%, p=0.039). The ATPC showed trends towards a better QoL score, assessed by a HFSR and QoL questionnaire at 9 weeks (26.0 vs. 29.9, p=0.574), and a lower frequency of discontinuation, interruption, or dose reduction of anticancer drugs (51.6% vs. 58.6%, p=0.586) than the PC group over 9 weeks, though without statistical significance.

Conclusion:

Our results showed that ATPC significantly decreased the development of grade ≥ 2 HFS/HFSR in patients already with HFS/HFSR. Therefore, ATPC may be an effective treatment for HFS/HFSR associated with anticancer drugs.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancer Res Treat Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancer Res Treat Year: 2024 Document type: Article