Incidence, Clinical Features, and Contributing Factors of Capecitabine-Related Hand–Foot Syndrome in Cancer Patients: Insights from Sudan - Scorecard - MDSpire

Incidence, Clinical Features, and Contributing Factors of Capecitabine-Related Hand–Foot Syndrome in Cancer Patients: Insights from Sudan

  • By

  • Ola K. Obeid

  • Bashir A. Yousef

  • Yousif B. Hamadalneel

  • Mawahib A. Mustafa

  • Amani Abdelaziz Mahmoud

  • Elkhanssa Abdelhameed Ahmed Elhag

  • April 3, 2026

  • 0 min

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Clinical Scorecard: Incidence, Clinical Features, and Contributing Factors of Capecitabine-Related Hand–Foot Syndrome in Cancer Patients: Insights from Sudan

At a Glance

CategoryDetail
ConditionCapecitabine-related hand–foot syndrome (HFS), a common chemotherapy-induced cutaneous toxicity
Key MechanismsInflammation or local trauma compromising capillary integrity; genetic polymorphisms affecting drug metabolism enzymes
Target PopulationAdult cancer patients receiving capecitabine monotherapy
Care SettingOncology hospital outpatient and inpatient settings, specifically Khartoum Oncology Hospital, Sudan

Key Highlights

  • More than 50% of Sudanese cancer patients on capecitabine develop HFS, impacting quality of life and treatment adherence.
  • Female sex and multiple chemotherapy cycles were associated with lower HFS incidence; absence of comorbidities increased risk.
  • Use of both NCI Common Terminology Criteria and a modified grading scale for Black patients improves HFS severity assessment.

Guideline-Based Recommendations

Diagnosis

  • Use standardized grading systems such as NCI Common Terminology Criteria for Adverse Events for HFS severity assessment.
  • Apply modified grading scales tailored for darker skin tones to improve diagnostic accuracy in Black patients.

Management

  • Early recognition and timely management of HFS to improve patient quality of life and maintain cancer treatment continuity.
  • Educate patients on signs and symptoms of HFS to facilitate prompt reporting and intervention.

Monitoring & Follow-up

  • Regular clinical evaluation during chemotherapy cycles to detect onset and progression of HFS.
  • Monitor patients especially those without concomitant diseases, as they have higher risk of developing HFS.

Risks

  • Higher risk of HFS in patients without concomitant diseases.
  • Ethnic and genetic factors may influence susceptibility to HFS.

Patient & Prescribing Data

Adult Sudanese cancer patients receiving capecitabine monotherapy at a national oncology center

Capecitabine monotherapy is associated with a high incidence of HFS; risk factors include absence of comorbidities and male sex; multiple chemotherapy cycles may reduce risk.

Clinical Best Practices

  • Restrict capecitabine monotherapy studies to isolate its specific contribution to HFS development.
  • Incorporate patient education on HFS symptoms and preventive measures as part of chemotherapy protocols.
  • Use dual grading systems for HFS severity to accommodate skin tone variations and improve clinical assessment.
  • Perform multivariable logistic regression analyses to identify independent risk factors for HFS.

References

Original Source(s)

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