SWOG clinical trial number
S1310
Randomized Phase II Trial of Single Agent MEK Inhibitor Trametinib Vs 5-Fluorouracil or Capecitabine in Refractory Advanced Biliary Cancer
Closed
Phase
Accrual
60%
Abbreviated Title
Rando PII GSK1120212 vs 5-FU/Leucovorin or Capecitabine for Refractory Advanced Biliary
Activated
02/15/2014
Closed
05/15/2015
Participants
Research committees
Gastrointestinal Cancer
Treatment
5-Fluorouracil
Leucovorin Calcium
Capecitabine
Trametinib Dimethyl Sulfoxide
Eligibility Criteria Expand/Collapse
Histologically or cytologically documented carcinoma primary to intra- or extra-hepatic biliary system or gall bladder with clinical/radiologic evidence of unresectable, locally advanced, or metastatic disease. Must have measurable disease. Must have completed prior chemotherapy at least 21 days prior to registration AND experienced progression to no more than 1 prior regimen of systemic chemo OR patients who received adjuvant chemo and had evidence of recurrence w/in 6 mo of completion of treatment. Must not have been treated with prior MEK inhibitors. Prior 5-FU or capecitabine allow only if given as radiosensitizer concurrently at least 12 wks prior to reg or if given as part of adjuvant therapy >/= 12 mo prior to enrollment. No plans to receive concurrent chemo, hormonal therapy, radiotherapy, immunotherapy, or other type of therapy for cancer. Must be >/= 28 days since cryotherapy, radiation therapy, radiofrequency ablation, therasphere, ethanol injection, TACE or photodynamic therapy. Zubrod PS 0-1. Within 28 days prior to reg: ANC > 1000/uL; platelets > 100,000/uL; total bilirubin </= 2.0 x IULN; AST & ALT both </= 3.0 x IULN; if liver mets present AST & ALT must be </= 5 x IULN. If pt has had decompression of biliary tree w/in 14 days stability of bilirubin level needs to be confirmed w/2 measurements. Serum creatinine </= 1.5 mg/dL or calculated creatinine clearance >/= 60 ml/min w/in 28 days prior to reg. Pts w/known history or current evidence of retinal vein occlusion or retinal pigment epithelial detachment are not eligible. LVEF >/= ILLN w/in 28 days prior to reg. Must not have uncontrolled/clinically significant cardiovascular disease including: MI w/in 6mo, uncontrolled angina w/in 6mo, class II-IV NYHA CHF, Grade 3 cardiac valve dysfunction, cardiac arrhythmia not controlled by meds, history of stroke or TIA w/in 6mo, history of ATE of any type in past 6 mo, treatment-refractory hypertension, known intra-cardiac defibrillators, or known cardiac metastases. QTcF
Publication Information Expand/Collapse
2020
PMid: PMID32234665 | PMC number: PMC7539324
Other Clinical Trials
SWOG Clinical Trial Number
S2303
Randomized Phase II/III Trial of 2nd Line Nivolumab + Paclitaxel + Ramucirumab versus Paclitaxel + Ramucirumab in Patients with PD-L1 CPS ≥ 1 Advanced Gastric and Esophageal Adenocarcinoma (PARAMUNE)
Research Committee(s)
Gastrointestinal Cancer
Activated
05/06/2024
Open
SWOG Clinical Trial Number
CTSU/A022101
A Pragmatic Randomized Phase III Trial Evaluating Total Ablative Therapy for Patients with Limited Metastatic Colorectal Cancer: Evaluating Radiation, Ablation, and Surgery (ERASur)
Research Committee(s)
Gastrointestinal Cancer
Activated
01/10/2023
Open
Phase
SWOG Clinical Trial Number
S2107
Randomized Phase II Trial of Encorafenib and Cetuximab with or Without Nivolumab (NSC #748726) for Patients with Previously Treated, Microsatellite Stable, BRAFV600E Metastatic and/or Unresectable Colorectal Cancer
Research Committee(s)
Gastrointestinal Cancer
Activated
06/06/2022
Accrual
100%
Open
Phase