Study on Chemotherapy and Radiation Therapy Followed by Chemotherapy for Localized Esophageal Cancer

Sponsor: Duke University

Sponsor score: 0

ClinicalTrials ID:NCT07603375

This clinical trial is exploring whether adding extra chemotherapy after the usual combination of chemotherapy and radiation can better control esophageal cancer and reduce the need for surgery.

Patient Parameters

Program Overview

The aim of this study is to find out if adding more chemotherapy after the standard treatment of chemotherapy and radiation can help control the spread and return of esophageal cancer, potentially reducing the need for surgery.

Eligibility Criteria

Inclusion Criteria

  • Must be able to give informed consent to participate in the study.
  • Newly diagnosed with adenocarcinoma of the thoracic esophagus or gastroesophageal junction.
  • Cancer stage II to IVA, but not T4b, according to specific medical guidelines.
  • Complete medical history and physical exam within 21 days before joining the study.
  • Recent whole-body scan to confirm no spread of cancer, done within 45 days before joining.
  • Good overall health with an ECOG performance status of 0 to 2.
  • Suitable for planned chemotherapy and radiation treatment as determined by medical specialists.
  • Adequate blood, kidney, and liver function within 14 days before starting treatment.

Exclusion Criteria

  • Cancer located in the cervical esophagus.
  • Esophageal squamous cell carcinoma.
  • Cancer stage T4b according to specific medical guidelines.
  • Evidence of cancer spread to other parts of the body.
  • Previous chemotherapy or radiation for the current cancer diagnosis.
  • Previous chest radiation that would overlap with current treatment areas.
  • Another progressing cancer that needs treatment, except for certain skin cancers or in situ cervical cancer.
  • Severe active health issues, such as uncontrolled infections needing IV antibiotics.
  • Pregnant or breastfeeding women.
  • HIV positive with a low CD4 count, unless under treatment and with a stable CD4 count.
  • Any physical or psychological issues that would prevent participation, as judged by the doctor.
  • Known psychiatric or substance abuse issues that would interfere with the study.

Locations

FACILITYZIPCITYSTATE
Duke University Medical Center27710DurhamNorth Carolina

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