Efficacy and Safety of OncoGel™ Added to Chemotherapy and Radiation Before Surgery in Subjects With Esophageal Cancer

This is an interventional treatment trial for Esophageal Cancer focused on measuring Esophageal cancer, Localized esophageal cancer, Operable esophageal cancer, Loco-regional esophageal cancer, Esophagectomy, Phase 2, Paclitaxel, Tumor, Local, Chemotherapy, radiation therapy, surgery, OncoGel, Squamous cell carcinoma of the esophagus Read More

Inclusion Criteria:

1. Histologically or cytologically confirmed squamous cell carcinoma or adenocarcinoma of the esophagus. Stage T2-T3, N any, M0 (no evidence of disseminated cancer except regional involvement which may be designated as "M1a"). No evidence of metastatic disease
2. Medically able to tolerate major abdominal and/or thoracic surgery
3. Able to undergo EUS procedure and pass EUS probe through esophageal lumen
4. Able to receive concurrent systemic chemotherapy (cisplatin and 5-FU) and RT
5. Clinical management plan includes esophagectomy after completion of two courses of chemoradiation therapy
6. Karnofsky Performance Status of ≥ 60
7. Minimum life expectancy of 4 months

8. Hematologic function

   • Absolute neutrophil count (ANC) ≥ 1500/mm3
   • Platelet count ≥ 100,000/mm3
   • Hemoglobin ≥ 9 g/dL

9. Hepatic function:

   • Total bilirubin < 1.5 X upper limit of normal (ULN)
   • AST and ALT < 3 X ULN
   • Albumin ≥ 3.0 g/dL or ≥ 2.0 g/dL if the lower level is considered by the investigator to be due to nutritional depletion
10. Serum creatinine < 1.5 mg/dL and/or creatinine clearance ≥ 65 mL/min
11. ≥ 18 years old
12. If female, must be non-pregnant, nonlactating, of non-childbearing potential, or using adequate birth control
13. Capable of understanding and agreeing to fulfill the requirements of the protocol
14. Sign the IRB/EC approved consent form

Exclusion Criteria:

1. History of anaphylaxis to planned CT contrast agent
2. Prior esophageal stent insertion, laser, or photodynamic therapy
3. Prior chest RT or major esophageal surgery
4. Any prior receipt of cytotoxic chemotherapeutic agents
5. Prior receipt of other cancer treatments (ie, Chelation therapy), vaccines, or biological response modifiers/growth factors (ie, GM-CSF, IL-2) within the past 4 weeks.
6. Prior malignancy unless disease free for ≥ 3 years. Note: basal cell/squamous carcinoma of the skin, in situ cervical or breast carcinoma, or superficial transitional cell bladder carcinoma will be allowed. Subjects with a history of low risk prostatic carcinoma (ie, clinical stage 1 or 2a, Gleason score < or = 6 and PSA <10 ng/mL at diagnosis) will be allowed
7. Significant currently active systemic diseases including uncontrolled diabetes, severe heart disease (New York Heart Association Class III or IV), uncontrolled hypertension, myocardial infarction within 3 months, severe bronchial obstruction, uncontrolled seizure disorder, or peripheral neuropathy greater than CTCAE grade 1
8. Allergies to any of the active or inactive components of OncoGel (ie, allergies to degradable PLGA [poly(lactide-co-glycolide) sutures])
9. Receipt of an investigational drug or device within 30 days prior to signing informed consent
10. Any medical condition or other circumstance that, in the Investigator's opinion, would prevent completion of the study, interfere with analysis of the study results, or potentially adversely affect subject safety
11. Known esophageal varices