Cisplatin, CPT-11 and Celecoxib With Radiation Therapy and Surgery for Operable Esophageal Cancer

• Status: Completed
• Trial end date: 2017-09-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a study for patients with resectable, locally advanced esophageal cancer. There is evidence to suggest that celecoxib in combination with cisplatin and irinotecan (CPT-11) may work well with radiation therapy to kill cancer cells. The primary goal is to develop a well-tolerated cancer treatment that has an acceptable response rate.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Dana-Farber Cancer Institute
• Collaborators: Brigham and Women's Hospital; Massachusetts General Hospital; Pharmacia
• Treatments: Celecoxib; Cisplatin; Irinotecan

Criteria

Inclusion Criteria:

• Age greater than or equal to 18 years.

• Adenocarcinoma or squamous cell carcinoma of the esophagus, including the gastroesophageal junction, histologically confirmed, American Joint Committee on Cancer (AJCC) Stage IIA, IIB, III. Additionally, patients with tumors of the lower thoracic esophagus and gastroesophageal junction may have regional lymph node involvement (M1A-Stage IVA), as long as the lymphadenopathy can be entirely encompassed by the radiation field.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

• Neutrophils greater than or equal to 1,500/ μL.

• Platelets greater than or equal to 100,000/ μL.

• Serum bilirubin less than or equal to 1.5 mg/dl.

• Serum creatinine less than or equal to 1.5 mg/dl.

• Aspartamine transaminase (AST or SGOT) less than or equal to 3x upper institutional normal limit.

• Alkaline phosphatase less than or equal to 5x upper institutional normal limit.

Exclusion Criteria:

• No prior surgery for esophageal or gastro-esophageal junction cancer.

• No prior chemotherapy or radiation therapy.

• Biopsy proven tumor invasion of the tracheobronchial tree or a tracheoesophageal fistula.

• Metastatic disease to distant organs (e.g. liver, lungs, bone) or non-regional lymph nodes. Patients with supraclavicular/cervical lymph node involvement or patients with a proximal esophageal primary and celiac/gastro-hepatic lymph node involvement are also excluded.

• Patients with co-morbid disease that, in the opinion of the investigator, makes combined chemo-radiotherapy inadvisable (e.g. New York State Grade III-IV heart disease, myocardial infarction in the last 4 months, uncontrolled infection, uncontrolled diabetes, uncontrolled hypertension, uncontrolled psychiatric illness or organ allograft(s) on immunosuppressive therapy).

• Pregnant or lactating women or women of childbearing potential with either a positive or no pregnancy test at baseline.

• Women of childbearing potential not using a reliable and appropriate contraceptive method. (Postmenopausal women must have been amenorrheic for at least 12 months to be considered of non-childbearing potential.)

• Other active malignancy (i.e. hematologic malignancy, metastatic solid tumor, or resected Stage I-IV solid tumor less than 3 years after resection).

• Patients with known Gilbert's disease or interstitial pulmonary fibrosis.

• Patients with prior severe reaction to nonsteroidal anti-inflammatory drugs (NSAIDs), sulfonamides, or celecoxib.

• Patients with a history of seizure disorders who are receiving antiepileptic medication.

• Positive malignant cytology of the pleura, pericardium or peritoneum.

• Uncontrolled diarrhea (National Cancer Institute Common Toxicity Criteria [NCI CTC] greater than or equal to Grade 2).

• Peripheral neuropathy (NCI CTC greater than or equal to Grade 2).

• Symptomatic hearing loss, requiring a hearing aid or for which a hearing aid has been suggested by a health professional.