Status:
TERMINATED
Regorafenib in Treating Patients With Locally Advanced Cancer of the Esophagus or Gastroesophageal Junction Who Have Completed Chemoradiation Therapy and Surgery
Lead Sponsor:
Academic and Community Cancer Research United
Collaborating Sponsors:
National Cancer Institute (NCI)
Conditions:
Adenocarcinoma of the Gastroesophageal Junction
Stage IIB Esophageal Adenocarcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This randomized phase II trial studies how well regorafenib works in treating patients with cancer of the esophagus or gastroesophageal junction that has spread from where it started to nearby tissue ...
Detailed Description
PRIMARY OBJECTIVES: I. To compare the disease-free survival (DFS) for patients with resected esophageal and gastroesophageal (GE) junction adenocarcinoma treated with regorafenib vs. placebo in the a...
Eligibility Criteria
Inclusion
- Histological confirmation of node positive (any T stage N1-3) proximal esophageal, distal esophagus or gastroesophageal (GE) junction adenocarcinoma (Siewert I, II, or III) after completing preoperative chemoradiation and surgery; supporting pathology report sufficient for registration; available tumor tissue from endoscopic biopsies prior to preoperative chemotherapy (chemo)/radiation therapy (RT), and tumor from surgical specimens will be submitted to Academic and Community Cancer Research United (ACCRU), but not be required prior registration; Note: if tissue is depleted, patient will still be eligible after discussion with the physician
- Imaging (computed tomography \[CT\] or magnetic resonance imaging \[MRI\]) =\< 28 days of study registration negative for disease recurrence
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
- Absolute neutrophil count (ANC) \>= 1500/mm\^3
- Platelet count \>= 100,000/mm\^3
- Total bilirubin =\< 1.5 x the upper limits of normal (ULN)
- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =\< 2.5 x ULN (=\< 5 x ULN for subjects with liver involvement of their cancer)
- Alkaline phosphatase limit =\< 2.5 x ULN (=\< 5 x ULN for subjects with liver involvement of their cancer)
- Lipase =\< 1.5 x the ULN
- Serum creatinine =\< 1.5 x the ULN
- International normalized ratio (INR)/partial thromboplastin time (PTT) =\< 1.5 x ULN; Note-subjects who are therapeutically treated with an agent such as warfarin or heparin will be allowed to participate provided that their medication dose and INR/PTT are stable; close monitoring (day 1 of each cycle) is mandatory; if either of these values is above the therapeutic range, the doses should be modified and the assessments should be repeated weekly until they are stable
- Negative pregnancy test done =\< 7 days prior to registration, for women of childbearing potential only
- Provide informed written consent
- Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase of the study)
- Able to swallow and retain oral medications and begin therapy within 6 to 12 weeks post-surgery
- Provide blood samples for the mandatory correlative research purposes
Exclusion
- Presence of metastatic or recurrent disease
- R1 or R2 resection
- Patients who have not recovered from serious adverse events (as determined by treating doctor of medicine \[MD\]) related to surgery
- Uncontrolled hypertension (systolic pressure \> 140 mm Hg or diastolic pressure \> 90 mm Hg on repeated measurement) despite optimal medical management per physician discretion
- Active or clinically significant cardiac disease including:
- Congestive heart failure - New York Heart Association (NYHA) \> class II
- Active coronary artery disease
- Cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin
- Unstable angina (anginal symptoms at rest), new-onset angina \< 3 months before randomization, or myocardial infarction within 6 months before randomization
- Evidence or history of bleeding diathesis or coagulopathy
- Any hemorrhage or bleeding event \>= National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4 grade 3 =\< 4 weeks prior to registration
- Prior cancers \< 3 years, with the exception of in-situ cervical cancer, low grade prostate cancer and basal or squamous cell skin cancers
- Subjects with thrombotic, embolic, venous, or arterial events, such as cerebrovascular accident (including transient ischemic attacks) deep vein thrombosis or pulmonary embolism =\< 6 months prior to registration
- Receiving any medications or substances that are strong or moderate inhibitors of cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4); use of strong or moderate inhibitors are prohibited =\< 7 days to registration
- Receiving any medications or substances that are inducers of CYP3A4; use of inducers are prohibited =\< 7 days prior to registration
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 8 2016
Estimated Enrollment :
3 Patients enrolled
Trial Details
Trial ID
NCT02234180
Start Date
September 1 2014
End Date
June 8 2016
Last Update
October 17 2018
Active Locations (10)
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1
Carle Cancer Center
Urbana, Illinois, United States, 61801
2
Cancer Center of Kansas - Wichita
Wichita, Kansas, United States, 67214
3
Ochsner Medical Center Jefferson
New Orleans, Louisiana, United States, 70121
4
Mayo Clinic
Rochester, Minnesota, United States, 55905