A Phase 1 Study of the DNA-PK Inhibitor Peposertib in Combination With Radiation Therapy With or Without Cisplatin in Patients With Advanced Head and Neck Tumors.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
24 Sep 2023
Historique:
received: 17 02 2023
revised: 05 09 2023
accepted: 14 09 2023
pubmed: 27 9 2023
medline: 27 9 2023
entrez: 26 9 2023
Statut: aheadofprint

Résumé

DNA-dependent protein kinase (DNA-PK) plays a key role in the repair of DNA double strand breaks via nonhomologous end joining. Inhibition of DNA-PK can enhance the effect of DNA double strand break inducing anticancer therapies. Peposertib (formerly "M3814") is an orally administered, potent, and selective small molecule DNA-PK inhibitor that has demonstrated radiosensitizing and antitumor activity in xenograft models and was well-tolerated in monotherapy. This phase 1 trial (National Clinical Trial 02516813) investigated the maximum tolerated dose, recommended phase 2 dose (RP2D), safety, and tolerability of peposertib in combination with palliative radiation therapy (RT) in patients with thoracic or head and neck tumors (arm A) and of peposertib in combination with cisplatin and curative-intent RT in patients with squamous cell carcinoma of the head and neck (arm B). Patients received peposertib once daily in ascending dose cohorts as a tablet or capsule in combination with palliative RT (arm A) or in combination with intensity modulated curative-intent RT and cisplatin (arm B). The most frequently observed treatment-emergent adverse events were radiation skin injury, fatigue, and nausea in arm A (n = 34) and stomatitis, nausea, radiation skin injury, and dysgeusia in arm B (n = 11). Based on evaluations of dose-limiting toxicities, tolerability, and pharmacokinetic data, RP2D for arm A was declared as 200 mg peposertib tablet once daily in combination with RT. In arm B (n = 11), 50 mg peposertib was declared tolerable in combination with curative-intent RT and cisplatin. However, enrollment was discontinued because of insufficient exposure at that dose, and the RP2D was not formally declared. Peposertib in combination with palliative RT was well-tolerated up to doses of 200 mg once daily as tablet with each RT fraction. When combined with RT and cisplatin, a tolerable peposertib dose yielded insufficient exposure.

Identifiants

pubmed: 37751793
pii: S0360-3016(23)07936-1
doi: 10.1016/j.ijrobp.2023.09.024
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Michael Samuels (M)

"Banner MD Anderson Cancer Center, Phoenix, Arizona, USA.

Johan Falkenius (J)

Theme Cancer, Karolinska University Hospital, Stockholm, Sweden.

Voichita Bar-Ad (V)

Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania.

Juergen Dunst (J)

Department of Radiotherapy, University Hospital Schleswig-Holstein, Lübeck, Germany.

Baukelien van Triest (B)

Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.

Jeffrey Yachnin (J)

Theme Cancer, Karolinska University Hospital, Stockholm, Sweden.

Almudena Rodriguez-Gutierrez (A)

Merck S.L.U., Madrid, Spain, an affiliate of Merck KGaA, Darmstadt, Germany.

Mirjam Kuipers (M)

The health care business of Merck KGaA, Darmstadt, Germany.

Xiaoli You (X)

EMD Serono, Billerica, MA, USA.

Barbara Sarholz (B)

The health care business of Merck KGaA, Darmstadt, Germany.

Giuseppe Locatelli (G)

The health care business of Merck KGaA, Darmstadt, Germany.

Andreas Becker (A)

The health care business of Merck KGaA, Darmstadt, Germany.

Esther G C Troost (EGC)

Department of Radiotherapy and Radiation Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; OncoRay - National Center for Radiation Research in Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany; Institute of Radiooncology - OncoRay, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany; National Center for Tumor Diseases, Partner Site Dresden, Germany; German Cancer Research Center, Heidelberg, Germany; Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany. Electronic address: Esther.Troost@uniklinikum-dresden.de.

Classifications MeSH