Literature DB >> 31028219

A Phase I Study of Napabucasin Plus Paclitaxel for Japanese Patients With Advanced/Recurrent Gastric Cancer.

Kohei Shitara1, Yasuhide Yodo2, Shuichi Iino2.   

Abstract

AIM: To report results from the first phase I study of napabucasin plus paclitaxel in Japanese patients with pre-treated unresectable/recurrent gastric cancer. PATIENTS AND METHODS: Patients received napabucasin (480 mg bid) plus paclitaxel [80 mg/m2 on days 3, 10 and 17 (cycles 1 and 2) and on days 1, 8 and 15 (cycle 3 and subsequent cycles)] until disease progression or unacceptable toxicity. Primary objectives were tolerability, safety and pharmacokinetics of napabucasin plus paclitaxel. Trial registration ID: JapicCTI-142420.
RESULTS: Six patients were enrolled. Paclitaxel had a minimal effect on napabucasin pharmacokinetics and median plasma paclitaxel concentrations were similar in combination and monotherapy. No dose-limiting toxicities were observed. There were no grade 4/5 adverse events. Partial response, stable disease and progressive disease were reported in two patients each.
CONCLUSION: Napabucasin plus paclitaxel was well-tolerated in Japanese patients with gastric cancer. Copyright
© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Entities:  

Keywords:  Napabucasin; cancer stem cells; gastric cancer

Mesh:

Substances:

Year:  2019        PMID: 31028219      PMCID: PMC6559899          DOI: 10.21873/invivo.11561

Source DB:  PubMed          Journal:  In Vivo        ISSN: 0258-851X            Impact factor:   2.155


  9 in total

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8.  Phase I study of napabucasin in combination with FOLFIRI + bevacizumab in Japanese patients with metastatic colorectal cancer.

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9.  Napabucasin Drug-Drug Interaction Potential, Safety, Tolerability, and Pharmacokinetics Following Oral Dosing in Healthy Adult Volunteers.

Authors:  Xiaoshu Dai; Michael D Karol; Matthew Hitron; Marjie L Hard; Matthew T Goulet; Colleen F McLaughlin; Scott J Brantley
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  9 in total

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