U.S. Phase I First-in-human Study of Taletrectinib (DS-6051b/AB-106), a ROS1/TRK Inhibitor, in Patients with Advanced Solid Tumors.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 28 04 2020
revised: 06 06 2020
accepted: 24 06 2020
pubmed: 28 6 2020
medline: 15 12 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

Taletrectinib (DS-6051b/AB-106) is an oral, tyrosine kinase inhibitor of ROS1 and NTRK with potent preclinical activity against Patients ≥18 years old with neuroendocrine tumors, with tumor-induced pain, or tumors harboring A total of 46 patients were enrolled. Steady-state peak concentration ( Taletrectinib has manageable toxicities at the MTD of 800 mg daily. Preliminary efficacy was observed in patients with crizotinib-refractory

Identifiants

pubmed: 32591465
pii: 1078-0432.CCR-20-1630
doi: 10.1158/1078-0432.CCR-20-1630
doi:

Substances chimiques

Imidazoles 0
NTRK1 protein, human 0
Protein Kinase Inhibitors 0
Proto-Oncogene Proteins 0
Pyridazines 0
Protein-Tyrosine Kinases EC 2.7.10.1
ROS1 protein, human EC 2.7.10.1
Receptor, trkA EC 2.7.10.1
taletrectinib W4141180YD

Types de publication

Clinical Trial, Phase I Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4785-4794

Informations de copyright

©2020 American Association for Cancer Research.

Auteurs

Kyriakos P Papadopoulos (KP)

South Texas Accelerated Research Therapeutics, San Antonio, Texas.

Erkut Borazanci (E)

HonorHealth and Translational Genomics Research Institute, Scottsdale, Arizona.

Alice T Shaw (AT)

Novartis Institute of BioMedical Research, Cambridge, Massachusetts.
Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Ryohei Katayama (R)

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yuki Shimizu (Y)

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.

Viola W Zhu (VW)

Chao Family Comprehensive Cancer Center, University of California, Irvine School of Medicine, Orange, California.

Thomas Yang Sun (TY)

Department of Medicine, Division of Oncology, Stanford University, Stanford Cancer Institute, Stanford, California.

Heather A Wakelee (HA)

Department of Medicine, Division of Oncology, Stanford University, Stanford Cancer Institute, Stanford, California.

Russell Madison (R)

Foundation Medicine Inc, Cambridge, Massachusetts.

Alexa B Schrock (AB)

Foundation Medicine Inc, Cambridge, Massachusetts.

Giorgio Senaldi (G)

Daiichi Sankyo, Inc., Basking Ridge, New Jersey.

Naoki Nakao (N)

Daiichi Sankyo RD Novare Co., Ltd, Tokyo, Japan.

Hiroyuki Hanzawa (H)

Daiichi Sankyo RD Novare Co., Ltd, Tokyo, Japan.

Masaya Tachibana (M)

Daiichi Sankyo, Co., Ltd, Tokyo, Japan.

Takeshi Isoyama (T)

Daiichi Sankyo, Co., Ltd, Tokyo, Japan.

Kenji Nakamaru (K)

Daiichi Sankyo, Co., Ltd, Tokyo, Japan.

Chenhui Deng (C)

Linking Truth Technology Co, Ltd, Beijing, China.

Meijing Li (M)

AnHeart Therapeutics (Hangzhou) Company Ltd, Hangzhou, Zhejiang province, China.

Frank Fan (F)

AnHeart Therapeutics (Hangzhou) Company Ltd, Hangzhou, Zhejiang province, China.

Qinying Zhao (Q)

AnHeart Therapeutics (Hangzhou) Company Ltd, Hangzhou, Zhejiang province, China.

Yanfei Gao (Y)

AnHeart Therapeutics (Hangzhou) Company Ltd, Hangzhou, Zhejiang province, China.

Takashi Seto (T)

Department of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

Pasi A Jänne (PA)

Dana-Faber Cancer Institute, Harvard Medical School, Boston, Massachusetts.

Sai-Hong Ignatius Ou (SI)

Chao Family Comprehensive Cancer Center, University of California, Irvine School of Medicine, Orange, California. siou@hs.uci.edu.

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Classifications MeSH