Cardiovascular safety of pimitespib in patients with advanced solid tumors: An open‐label, nonrandomized, phase 1 study

Author:

Naoki Katsuhiko1ORCID,Igawa Satoshi1,Uojima Haruki2,Tsumura Hideyasu3ORCID,Sengoku Norihiko4,Karayama Masato5,Shimomura Akihiko6ORCID,Ohtake Tohru7,Shio Yutaka8,Hosokawa Ayumu9,Komatsu Yoshito10,Kumagai Yuji11

Affiliation:

1. Department of Respiratory Medicine Kitasato University School of Medicine Sagamihara Kanagawa Japan

2. Department of Gastroenterology Kitasato University School of Medicine Sagamihara Kanagawa Japan

3. Department of Urology Kitasato University School of Medicine Sagamihara Kanagawa Japan

4. Department of Breast and Endocrine Surgery Kitasato University School of Medicine Sagamihara Kanagawa Japan

5. Department of Chemotherapy Hamamatsu University School of Medicine Hamamatsu Shizuoka Japan

6. Department of Breast and Medical Oncology National Center for Global Health and Medicine Tokyo Japan

7. Department of Breast Surgery Fukushima Medical University Hospital Fukushima Japan

8. Department of Chest Surgery Fukushima Medical University Hospital Fukushima Japan

9. Department of Clinical Oncology University of Miyazaki Hospital Miyazaki Japan

10. Department of Cancer Center Hokkaido University Hospital Sapporo Hokkaido Japan

11. Department of Research Clinical Trial Center Kitasato University Kitasato Institute Hospital Tokyo Japan

Abstract

AbstractBackgroundPimitespib (TAS‐116), a first‐in‐class, oral, selective heat‐shock protein 90 inhibitor, is approved as fourth‐line treatment for gastrointestinal stromal tumors in Japan. This phase 1 study evaluated the cardiac safety of pimitespib.MethodsIn this open‐label, nonrandomized, multicenter study, Japanese patients (aged ≥20 years) with refractory, advanced solid tumors received placebo on day −1, then pimitespib 160 mg daily on days 1–5 of the cardiac safety evaluation period. Electrocardiograms were conducted at baseline, and on days −2, −1, 1, and 5; and blood samples were collected on days 1 and 5. Patients then received once‐daily pimitespib for 5 days every 3 weeks. The primary end point was the time‐matched difference in QT interval corrected for heart rate using the Fridericia correction (QTcF) between pimitespib and placebo. Pharmacokinetics, safety, and preliminary efficacy were also assessed.ResultsOf the 22 patients in the cardiac safety‐evaluable population, no clinically relevant QTc prolongation was observed; the upper bound of the one‐sided 95% confidence interval for the time‐matched difference in change from baseline in QTcF was <20 msec at all time points on days 1 and 5. Pimitespib pharmacokinetic parameters were consistent with previous data, and the time‐matched difference in change from baseline in QTcF showed no marked increase as plasma concentrations increased. The safety profile was acceptable; 40% of patients experienced grade 3 or greater adverse drug reactions, mostly diarrhea (20%). The median progression‐free survival was 3.1 months.ConclusionsIn Japanese patients with refractory, advanced solid tumors, pimitespib was not associated with clinically relevant QTc prolongation, and there were no cardiovascular safety concerns.Plain Language Summary Pimitespib is a new anticancer drug that is being used to treat cancer in the stomach or intestines (gastrointestinal stromal tumors). This study demonstrated that pimitespib had no marked effect on heart rhythm or negative effects on the heart or blood vessels and had promising anticancer effects in Japanese patients with advanced solid tumors who were unable to tolerate or benefit from standard treatment.

Publisher

Wiley

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