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March 6, 2026JAMA Dermatology3 citations

Preventing Hand-Foot Syndrome in Patients With Cancer

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HBHemavathi BaskaraneSSShubham SahniCNChitrakshi Nagpal

Key Points

  • The aim is to evaluate the efficacy of pharmacologic interventions in preventing chemotherapy-induced hand-foot syndrome.
  • Systematic search of PubMed, Embase, and Cochrane CENTRAL for relevant RCTs.
  • Inclusion of phase 2 or 3 trials comparing systemic or topical prophylactic interventions.
  • Data extracted by two reviewers with a focus on risk of bias using the Cochrane tool.
  • Frequentist random-effects network meta-analysis performed.
  • Nineteen RCTs included, with 17 analyzed involving 2192 patients.
  • Topical silymarin and diclofenac significantly reduced grade 2 or higher HFS compared to placebo.
  • Diclofenac also decreased overall HFS incidence, while silymarin did not show benefit for overall HFS.
  • Mapisal was associated with an increased risk of HFS.

Abstract

Importance Hand-foot syndrome (HFS) is a common dose-limiting toxic effect of several chemotherapy agents, particularly capecitabine. Despite its substantial impact on the patient’s quality of life and potential to compromise therapeutic efficacy, effective preventive strategies remain limited. Objective To evaluate and compare the efficacy of pharmacologic interventions for the prevention of chemotherapy-induced HFS through a network meta-analysis of published results of randomized clinical trials (RCTs). Data Sources PubMed, Embase, and Cochrane CENTRAL were systematically searched from inception through November 2024 for relevant RCTs. Study Selection Eligible studies were phase 2 or 3 RCTs that compared systemic or topical prophylactic interventions for the prevention of HFS. Data Extraction and Synthesis Data extraction was performed by 2 reviewers, and disagreements were resolved by consensus. Risk of bias was assessed using the Cochrane Risk of Bias tool. A frequentist random-effects network meta-analysis was conducted. Main Outcomes and Measures The primary income was incidence of grade 2 or higher HFS. The secondary outcome was the incidence of any-grade HFS. Odds ratios (ORs) with 95% CIs were estimated. Ranking was assessed using P-scores and surface under the cumulative ranking (SUCRA) values. Results Nineteen RCTs were included, of which 17 trials comprising 2192 patients (median range age, 57 56-61 years) were analyzed for the primary outcome. Compared with placebo, topical silymarin (OR, 0.08; 95% CI, 0.01-0.71), diclofenac (OR, 0.23; 95% CI, 0.08-0.62), 400-mg pyridoxine (OR, 0.28; 95% CI, 0.09-0.88), and celecoxib (OR, 0.41; 95% CI, 0.18-0.95) significantly reduced grade 2 or higher HFS. Diclofenac (OR, 0.30; 95% CI, 0.13-0.69) and celecoxib (OR, 0.46; 95% CI, 0.22-0.94) also reduced overall HFS incidence. In contrast, silymarin and 400-mg pyridoxine did not show benefit for overall HFS, while mapisal increased HFS risk (OR, 3.04; 95% CI, 1.07-8.64). Ranking analyses showed the highest SUCRA value for silymarin (0.91) and diclofenac (0.76). Conclusions and Relevance In this systematic review and network meta-analysis, diclofenac and silymarin were the most effective preventive strategies for HFS, with silymarin requiring confirmation in a larger randomized trial. Diclofenac emerged as the agent with the best overall supporting evidence, informed by both effect estimates and study quality.

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Cite This Study

Baskarane et al. (2026) studied this question.

synapsesocial.com/papers/69aa7077531e4c4a9ff5a503https://doi.org/10.1001/jamadermatol.2026.0042
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