Chemoradiotherapy for Advanced Esophageal Cancer (PaRCUS)

AHS Cancer Control Alberta

Status and phase: Enrolling; Phase 2

Conditions: Esophageal Cancer

Treatments: Radiation: External Beam Radiation; Drug: Carboplatin and Taxol (paclitaxel)

Study type: Interventional

Funder types: Other

Identifiers

NCT02297217

HREBA.CC-14-0122

Details and patient eligibility

About

This study aims to show that the addition of carboplatin and paclitaxel chemotherapy to a palliative course of external beam radiation treatment improves both dysphagia relief and patient quality of life in patients with unresectable esophageal cancer.

Full description

Patients with carcinoma of the esophagus not suitable for definitive radical treatment who have symptomatic dysphagia requiring locoregional palliation, and who have no contra-indications to chemo-radiotherapy will be offered Carboplatin (AUC 2) and paclitaxel (50 mg/m2) intravenously on days 1 and 8 concurrent with external beam radiation therapy of 30Gy/10 fractions over two weeks where the primary goal is relief of dysphagia and other outcomes include toxicity, quality of life and metabolomics.

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Biopsy proven carcinoma of the esophagus.

2. Not a candidate for radical/curative treatment due to the advanced nature of the disease, presence of metastases, or intercurrent illness.

3. Symptomatic patients with Mellow Dysphagia Scores of ≥ 1 i.e. able to eat only some solids.

4. ECOG Performance status ≤ 2.

5. Patients able to begin treatment within 14 days of signing the informed consent form.

6. Patient is at least 18 years old.

7. Hematological function as defined by the following laboratory parameters:

   • Hemoglobin > 100g/L
   • Platelet count > 100x10E9/L
   • Absolute neutrophil count > 1.5x10E9/L

8. Renal function to undergo chemotherapy as defined by the following laboratory parameters:

   • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5x the upper limit of institutional normal (≤ 5 if liver metastases)
   • Total bilirubin ≤ 1.5x the upper limit of institutional normal
   • Calculated creatinine clearance ≥ 50 mL/min using the Cockcroft-Gault formula

9. Patients capable of childbearing are using adequate contraception.

10. Written and informed consent of patient.

Exclusion criteria

1. Previous radiotherapy delivered to the chest.
2. Synchronous active malignancies.
3. Pregnant or lactating patients: women of child bearing potential must have a negative serum pregnancy test within 7 days of Treatment Visit 1. Women or men of child bearing potential must use effective contraception (defined by the use of two birth control methods, which can be either two barrier methods or a barrier method plus a hormonal method to prevent pregnancy). Subjects must start using birth control from the time they have signed the Informed Consent Form prior to start of therapy until 120 days post completion of study therapy or study discontinuation, which must be documented in the eCRF.
4. Patients unfit for any treatment component, including absolute contraindications for radiotherapy or Connective Tissue Disease.
5. Tracheo-esophageal fistula.
6. Esophageal stents in situ.
7. Previous chemotherapy for esophageal cancer
8. Unable to complete surveys in English without aid of interpreter.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Chemotherapy with Concurrent Radiation

Experimental group

Description:

Carboplatin and paclitaxel will be administered intravenously on Days 1 and 8 while radiation therapy is administered

Treatment:

Radiation: External Beam Radiation

Drug: Carboplatin and Taxol (paclitaxel)