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Alkylating agents, Anti-tumor antibiotic

Chemoradiotherapy for Esophageal Cancer (PaRCUS Trial)

Phase 2
Recruiting
Led By Marc Kerba, MD
Research Sponsored by AHS Cancer Control Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Biopsy proven carcinoma of the esophagus
Not a candidate for radical/curative treatment due to the advanced nature of the disease, presence of metastases, or intercurrent illness
Must not have
Previous radiotherapy delivered to the chest
Synchronous active malignancies
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights

Summary

This trial tests if adding certain chemotherapy drugs to radiation therapy can better relieve swallowing difficulties and improve quality of life for patients with advanced esophageal cancer who can't undergo surgery. These drugs are commonly used in treatment for esophageal cancer and have shown promising results in various studies.

Who is the study for?
This trial is for adults with advanced esophageal cancer who can eat some solids, have a decent performance status, and proper organ function. They must start treatment within two weeks of consent, not be pregnant or breastfeeding, use effective contraception, and cannot have had previous chest radiation or chemotherapy for esophageal cancer.
What is being tested?
The study tests if adding carboplatin and paclitaxel (chemotherapy drugs) to external beam radiation improves swallowing difficulties and life quality in patients with inoperable esophageal cancer compared to radiation alone.
What are the potential side effects?
Possible side effects include nausea, vomiting, hair loss from chemotherapy; fatigue from both treatments; lowered blood counts leading to increased infection risk; kidney or liver stress shown by lab tests; and potential damage to nearby organs from radiation.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My esophageal cancer has been confirmed by a biopsy.
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My condition cannot be cured due to its advanced stage or other health issues.
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I can only eat some solid foods due to my swallowing difficulty.
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I am 18 years old or older.
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I can take care of myself but might not be able to do heavy physical work.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had radiation therapy to my chest before.
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I have more than one type of cancer at the same time.
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I cannot undergo certain treatments due to my health condition.
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I have a connection between my windpipe and esophagus.
Select...
I have had chemotherapy for esophageal cancer.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Proportion of patients who achieve relief of dysphagia
Secondary study objectives
Dysphagia progression free survival

Trial Design

1Treatment groups
Experimental Treatment
Group I: Chemotherapy with Concurrent RadiationExperimental Treatment2 Interventions
Carboplatin and paclitaxel will be administered intravenously on Days 1 and 8 while radiation therapy is administered
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
External Beam Radiation
2014
Completed Phase 2
~70

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Carboplatin and Paclitaxel are common treatments for esophageal cancer. Carboplatin causes DNA crosslinking, which prevents DNA replication and transcription, leading to cell death. Paclitaxel stabilizes microtubules, preventing their disassembly, which is crucial for cell division, thereby halting the cell cycle and inducing apoptosis. These mechanisms are important for esophageal cancer patients as they target rapidly dividing cancer cells, reducing tumor growth and potentially improving symptoms and survival rates.

Find a Location

Who is running the clinical trial?

AHS Cancer Control AlbertaLead Sponsor
182 Previous Clinical Trials
26,781 Total Patients Enrolled
Marc Kerba, MDPrincipal Investigator403 521 3164

Media Library

Carboplatin and Taxol (paclitaxel) (Alkylating agents, Anti-tumor antibiotic) Clinical Trial Eligibility Overview. Trial Name: NCT02297217 — Phase 2
Esophageal Cancer Research Study Groups: Chemotherapy with Concurrent Radiation
Esophageal Cancer Clinical Trial 2023: Carboplatin and Taxol (paclitaxel) Highlights & Side Effects. Trial Name: NCT02297217 — Phase 2
Carboplatin and Taxol (paclitaxel) (Alkylating agents, Anti-tumor antibiotic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT02297217 — Phase 2
~9 spots leftby Sep 2025