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

Esophageal Cancer Clinical Trial

Official title:

Phase II Trial of Cisplatin, CPT-11, Celecoxib (PCC), Concurrent Radiation Therapy, and Surgery for Resectable Esophageal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00137852
• Other study ID #: 01-229
• Status: Completed
• Phase: Phase 2
• First received: August 29, 2005
• Last updated: September 18, 2017
• Start date: January 2002
• Est. completion date: September 2017

Study information

• Verified date: September 2017
• Source: Dana-Farber Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Patients will take celecoxib orally twice daily 3 days prior to radiation therapy and until one week prior to surgery. Celecoxib will then be restarted when the patient is discharged from the hospital following surgery and continued for 26 weeks.

Patients will receive chemotherapy (cisplatin and irinotecan) weekly on weeks 1, 2, 4 and 5 during radiation therapy. Chemotherapy must occur on or before the fifth day of radiation therapy.

Radiation therapy will be performed 5 days a week over a 5.6 week period.

Patients will undergo an esophagectomy within 4-8 weeks of chemotherapy/radiation therapy. Technically accessible lymph nodes will also be removed.

During chemotherapy/radiation therapy, a physical exam and bloodwork will be conducted weekly.

Between chemotherapy/radiation therapy and surgery a physical exam, bloodwork and CT of chest, abdomen, and pelvis should be performed.

After the completion of treatment and surgery, a physical exam and bloodwork should be done every 6 weeks for 6 months, then every 3 months for 1 1/2 years, then every 6 months for 3 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: September 2017
• Est. primary completion date: August 2004
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Esophageal Cancer
• Esophageal Neoplasms

Intervention

Drug:
• Cisplatin
Given weekly on weeks 1, 2, 4 and 5 during radiation therapy.
• Irinotecan
Given weekly on weeks 1, 2, 4 and 5 during radiation therapy
• Celecoxib
Given twice daily 3 days prior to radiation and up until one week prior to surgery. It will then be started again once the participant is released from the hospital following surgery for 26 weeks.

Procedure:
• Radiation Therapy
5 days a week for 5-6 weeks
• Esophagectomy
Within 4-8 weeks of chemoradiation therapy

Locations

Country	Name	City	State
United States	Dana-Farber Cancer Institute	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (4)

Lead Sponsor	Collaborator
Dana-Farber Cancer Institute	Brigham and Women's Hospital, Massachusetts General Hospital, Pharmacia

Country where clinical trial is conducted

United States, 

References & Publications (1)

Cleary JM, Mamon HJ, Szymonifka J, Bueno R, Choi N, Donahue DM, Fidias PM, Gaissert HA, Jaklitsch MT, Kulke MH, Lynch TP, Mentzer SJ, Meyerhardt JA, Swanson RS, Wain J, Fuchs CS, Enzinger PC. Neoadjuvant irinotecan, cisplatin, and concurrent radiation the — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response rate of combination of chemotherapy, radiation therapy and surgery in resectable esophageal carcinoma		TBD
Secondary	Determine the side effects of chemotherapy and radiation therapy in patients with resectable esophageal carcinoma		2 years