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Efficacy and safety of trametinib in Japanese patients with advanced biliary tract cancers refractory to gemcitabine.
- Source :
-
Cancer science [Cancer Sci] 2018 Jan; Vol. 109 (1), pp. 215-224. Date of Electronic Publication: 2017 Dec 09. - Publication Year :
- 2018
-
Abstract
- Gemcitabine-based therapy remains the mainstay of treatment for patients with biliary tract cancers (BTCs) with no second-line treatment(s) established yet. Aberrant activation of the MAPK pathway in patients with BTC indicates its importance in BTC. Trametinib is a potent, highly selective, allosteric non-competitive inhibitor of MEK1/MEK2. In this phase IIa open-label, single-arm study, we investigated the efficacy and safety of trametinib in Japanese patients with advanced BTC refractory to gemcitabine-based therapy. All patients received oral trametinib 2 mg once daily until progressive disease (PD), death, or unacceptable toxicity. The primary objective was to determine the 12-week non-PD rate. Secondary assessments included safety, progression-free survival (PFS), overall survival, and overall response rate. Targeted exome sequencing was used to identify biomarkers for sensitivity or resistance to trametinib monotherapy. Twenty patients (median age, 61.5 years) with carcinoma of gall bladder (40%), intrahepatic (25%) or extrahepatic (30%) bile duct, and ampulla of Vater (5%) were enrolled. The non-PD rate at week 12 was 10% (95% confidence interval, 1.2-31.7); it did not reach the threshold rate of 25%. Median PFS was 10.6 weeks (95% confidence interval, 4.6-12.1) and 1-year overall survival was 20.0%. Stable disease and PD were observed in 13 (65%) and seven (35%) patients, respectively. No new safety signals were reported. Although the primary end-point was not met, prolonged PFS was observed in one patient having six somatic variants including synonymous NF1 exon 12 splice variant and a loss-of-function variant in ARID1A. Efforts to understand responsive mutations and sensitivity to targeted therapies are warranted. This trial was registered with ClinicalTrials.gov: NCT01943864.<br /> (© 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.)
- Subjects :
- Administration, Oral
Aged
Aged, 80 and over
Ampulla of Vater pathology
DNA-Binding Proteins
Female
Humans
Male
Middle Aged
Neurofibromin 1 genetics
Nuclear Proteins genetics
Protein Kinase Inhibitors adverse effects
Pyridones adverse effects
Pyrimidinones adverse effects
Survival Analysis
Transcription Factors genetics
Treatment Outcome
Exome Sequencing
Bile Duct Neoplasms drug therapy
Biliary Tract Neoplasms drug therapy
Gallbladder Neoplasms drug therapy
Protein Kinase Inhibitors administration & dosage
Pyridones administration & dosage
Pyrimidinones administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1349-7006
- Volume :
- 109
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cancer science
- Publication Type :
- Academic Journal
- Accession number :
- 29121415
- Full Text :
- https://doi.org/10.1111/cas.13438