TAS-102 Plus Radiotherapy in Elderly ESCC

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age65-85
SponsorQianfoshan Hospital

About this trial

This study is a single-arm, multicenter clinical trial evaluating the efficacy and safety of radiotherapy combined with TAS-102 monotherapy in elderly patients with locally advanced esophageal cancer.

Treatment Phase: The treatment phase is divided into a Phase I stage and a Phase II stage. The Phase I stage aims to explore the maximum tolerated dose (MTD) of TAS-102 in elderly esophageal cancer patients. A total of 9 subjects were enrolled, and the dose was escalated from 30 mg/m² in 5 mg/m² increments up to 40 mg/m². The MTD was defined as the highest drug dose at which no dose-limiting toxicity (DLT) was observed in more than 40% of treated patients during the first two weeks of combined radiotherapy and TAS-102 administration. The Phase II stage aims to investigate the efficacy of radiotherapy combined with TAS-102 at the MTD in elderly esophageal cancer patients, with 36 subjects enrolled.

Consolidation Phase: Following the treatment phase, subjects had a 3-4 week rest period. This was followed by consolidation therapy with TAS-102 monotherapy at a dose of 35 mg/m², administered twice daily on days 1-5 of a 28-day cycle for two cycles.

Subsequently, patients entered the efficacy and safety follow-up phase until the study endpoints were reached or after a full 2-year follow-up period.

Eligibility criteria

Qualifiers

Patients must have newly confirmed histologically or cytologically diagnosed esophageal squamous cell carcinoma.

Age between 65 and 85 years.

Esophageal cancer staged as IIB to IVB according to the 8th edition AJCC staging system (including IVB with supraclavicular or celiac lymph node metastasis, but excluding IVB with other distant metastases).

ECOG performance status of 0 or 1.

Disqualifiers

Patients with hematogenous metastasis or distant lymph node metastasis (except supraclavicular or celiac lymph node metastasis), multiple esophageal cancer lesions, or malignant pleural/pericardial effusion.

History of radiotherapy, chemotherapy, or surgery targeting the primary tumor or lymph nodes.

Tracheoesophageal fistula, invasion of the trachea or main bronchi by the primary tumor, deep esophageal ulcer, or hematemesis.

Severe comorbidities such as active infection, cardiovascular disease, or pulmonary disease.

Trial design

Treatments tested in this trial

  • TAS-102
  • Radiotherapy

Treatment groups

45 Participants
are divided into 1 treatment group

Locations

1
The First Affiliated Hospital of Shandong First Medical University250000, JinanShandong, China

Sponsors and collaborators

Qianfoshan Hospital

Lead sponsor