Phase 2
N=40
Neoadjuvant Paclitaxel Poliglumex, Cisplatin and Radiation for Esophageal Cancer: A Phase II Trial (CTI#X64001)
Esophageal Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00522795 ↗Enrolled (actual)
40
Serious AEs
35.0%
Results posted
Aug 2013
Primary outcome: Primary: Complete Pathologic Response — 12 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- PPX with cisplatin and radiation (Drug)
- Age
- Adult, Older Adult · 19+ yrs
- Sex
- All
- Sponsor
- Brown University
- Primary completion
- Feb 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Complete Pathologic Response |
12 | — |
Summary
Neoadjuvant Paclitaxel Poliglumex (PPX; CT-2103), Cisplatin and Radiation for Esophageal Cancer: A Phase II Trial. (CTI#X64001
Eligibility Criteria
Inclusion Criteria
- Patients are required to have pathologically confirmed adenocarcinoma or squamous cell carcinoma of the esophagus or gastroesophageal junction
- Patients may have celiac adenopathy
- There must be no evidence of distant organ metastases
- No prior chemotherapy or radiation for esophageal cancer
- Patients must be > 18 years of age, and non pregnant
- Patients must have an ANC > 1,500/ul, platelets > 100,000/ul, creatinine < 2.0 and bilirubin < 1.5 x ULN-ECOG performance status 0-1.
- Female patients, must either be not of child bearing potential or have a negative pregnancy test within 14 days of starting study treatment. Patients are considered not of child bearing potential if they are surgically sterile (they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal. Pregnant or lactating females are not eligible
- No contraindications to esophagectomy
- Signed informed consent
Exclusion Criteria
- Active or uncontrolled infection
- Patients must not have other coexistent medical condition that would preclude protocol therapy.
- Any concurrent chemotherapy not indicated in the study protocol or any other investigational agent(s).
Data sourced from ClinicalTrials.gov (NCT00522795). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.