Tucatinib and Trastuzumab for Previously Treated Human Epidermal Growth Factor Receptor 2-Positive Metastatic Biliary Tract Cancer (SGNTUC-019): A Phase II Basket Study.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
26 Sep 2023
Historique:
pubmed: 26 9 2023
medline: 26 9 2023
entrez: 26 9 2023
Statut: aheadofprint

Résumé

To evaluate the efficacy and safety of tucatinib and trastuzumab in patients with previously treated human epidermal growth factor receptor 2-positive (HER2+) metastatic biliary tract cancer (mBTC). SGNTUC-019 (ClinicalTrials.gov identifier: NCT04579380) is an open-label phase II basket study evaluating the efficacy and safety of tucatinib and trastuzumab in patients with HER2-altered solid tumors. In the biliary tract cancer cohort, patients had previously treated HER2 overexpressing or amplified (HER2+) tumors (identified with local testing) with no prior HER2-directed therapy. The primary end point was confirmed objective response rate (cORR) per investigator assessment. Patients were treated on a 21-day cycle with tucatinib (300 mg orally twice daily) and trastuzumab (8 mg/kg intravenously followed by 6 mg/kg every 3 weeks). Thirty patients were enrolled. As of data cutoff (January 30, 2023), the median duration of follow-up was 10.8 months. The cORR was 46.7% (90% CI, 30.8 to 63.0), with a disease control rate of 76.7% (90% CI, 60.6 to 88.5). The median duration of response and progression-free survival were 6.0 months (90% CI, 5.5 to 6.9) and 5.5 months (90% CI, 3.9 to 8.1), respectively. At data cutoff, 15 patients (50.0%) had died, and the estimated 12-month overall survival rate was 53.6% (90% CI, 36.8 to 67.8). The two most common treatment-emergent adverse events (TEAEs) were pyrexia (43.3%) and diarrhea (40.0%). Grade ≥3 TEAEs were reported in 18 patients (60.0%), with the most common being cholangitis, decreased appetite, and nausea (all 10.0%), which were generally not treatment related. TEAEs led to treatment regimen discontinuation in one patient, and there were no deaths due to TEAEs. Tucatinib combined with trastuzumab had clinically significant antitumor activity and was well tolerated in patients with previously treated HER2+ mBTC.

Identifiants

pubmed: 37751561
doi: 10.1200/JCO.23.00606
doi:

Banques de données

ClinicalTrials.gov
['NCT04579380']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

JCO2300606

Auteurs

Yoshiaki Nakamura (Y)

National Cancer Center Hospital East, Kashiwa, Japan.

Nobumasa Mizuno (N)

Aichi Cancer Center Hospital, Nagoya, Japan.

Yu Sunakawa (Y)

St Marianna University Hospital, Kawasaki, Japan.

Jean-Luc Canon (JL)

Grand Hospital de Charleroi, Charleroi, Belgium.

Matthew D Galsky (MD)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Erika Hamilton (E)

Sarah Cannon Research Institute/Tennessee Oncology, Nashville, TN.

Hidetoshi Hayashi (H)

Kindai University Hospital, Osakasayama, Japan.

Guy Jerusalem (G)

CHU de Liege and Liege University, Liege, Belgium.

Seung Tae Kim (ST)

Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, South Korea.

Keun-Wook Lee (KW)

Seoul National University College of Medicine and Seoul National University Bundang Hospital, Seongnam, South Korea.

Lionel Aurelien Kankeu Fonkoua (LA)

Mayo Clinic Rochester, Rochester, MN.

Bradley J Monk (BJ)

HonorHealth Research Institute, University of Arizona, Creighton University, Phoenix, AZ.

Danny Nguyen (D)

City of Hope National Medical Center, Duarte, CA.

Do-Youn Oh (DY)

Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Integrated Major in Innovative Medical Science, Seoul National University Graduate School, Seoul, South Korea.

Alicia Okines (A)

The Royal Marsden NHS Foundation Trust, London, UK.

David M O'Malley (DM)

The Ohio State University & James Comprehensive Cancer Center, Columbus, OH.

Paula Pohlmann (P)

MD Anderson Cancer Center, Houston, TX.

Martin Reck (M)

Department of Thoracic Oncology, Airway Research Center North, Germany Center for Lung Disease, Grosshansdorf, Germany.

Sang Joon Shin (SJ)

Severance Hospital, Yonsei University Health System, Seoul, South Korea.

Kazuki Sudo (K)

National Cancer Center, Tokyo, Japan.

Shunji Takahashi (S)

Cancer Institute Hospital of JFCR, Tokyo, Japan.

Cedric Van Marcke (C)

Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Evan Y Yu (EY)

Fred Hutchinson Cancer Center/University of Washington, Seattle, WA.

Jorge Ramos (J)

Seagen Inc, Bothell, WA.

Sherry Tan (S)

Seagen Inc, Bothell, WA.

Thomas E Stinchcombe (TE)

Duke Cancer Institute, Durham, NC.

Tanios Bekaii-Saab (T)

Mayo Clinic Scottsdale, Scottsdale, AZ.

Classifications MeSH