Clin2
NCT05940441Possibly a fitRecruiting

Low-dose capecitabine after throat cancer treatment

to Explore Whether the Adjuvant Therapy of Metronomic Capecitabine Could Improve the Disease-free Survival of Locoregionally Advanced Hypopharyngeal Carcinoma

Treatments studied

Part of Cancer, Ear, nose & throat clinical trials.

This study tests whether low-dose capecitabine given after standard treatment can lower the chance that locoregional (nearby) throat cancer returns. It is designed for adults with advanced hypopharyngeal (throat) cancer who have finished curative chemoradiation or surgery and follow-up therapy and show no active cancer on exam.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
74 people
Ages
18 years to 65 years
Study type
Observational

Who can take part

  • You’re between 18 and 65 years old.
  • Your diagnosis is hypopharyngeal (throat) cancer, stage IV by the study’s staging rules, and you completed the standard curative treatment (either chemoradiation or surgery plus follow-up therapy).
  • After your definitive chemoradiotherapy, doctors do not see any remaining nearby tumor or distant spread.
  • You are starting the study within 8 weeks after your last radiation treatment.
  • Your body can safely tolerate the study: blood counts, liver tests, and kidney function are within allowed ranges, and your activity level is ECOG 0–1 (able to carry out daily activities).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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