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Results of an open-label phase 1b study of the ERK inhibitor MK-8353 plus the MEK inhibitor selumetinib in patients with advanced or metastatic solid tumors.
Stathis, Anastasios; Tolcher, Anthony W; Wang, Judy S; Renouf, Daniel J; Chen, Lin-Chi; Suttner, Leah H; Freshwater, Tomoko; Webber, Andrea L; Nayak, Tapan; Siu, Lillian L.
Afiliação
  • Stathis A; Oncology Institute of Southern Switzerland, EOC, via A. Gallino 12, Bellinzona 6500, Switzerland. anastasios.stathis@eoc.ch.
  • Tolcher AW; NEXT Oncology, San Antonio, TX, USA.
  • Wang JS; Florida Cancer Specialists/Sarah Cannon Research Institute, Sarasota, FL, USA.
  • Renouf DJ; BC Cancer-Vancouver Center, Vancouver, BC, Canada.
  • Chen LC; Merck & Co., Inc., Rahway, NJ, USA.
  • Suttner LH; Merck & Co., Inc., Rahway, NJ, USA.
  • Freshwater T; Merck & Co., Inc., Rahway, NJ, USA.
  • Webber AL; Merck & Co., Inc., Rahway, NJ, USA.
  • Nayak T; Merck & Co., Inc., Rahway, NJ, USA.
  • Siu LL; Princess Margaret Cancer Centre, Toronto, ON, Canada.
Invest New Drugs ; 41(3): 380-390, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37040046
ABSTRACT

AIM:

We evaluated MK-8353 (small molecule inhibitor of extracellular signal-regulated kinase 1/2) plus selumetinib (mitogen-activated extracellular signal-regulated kinase 1/2 inhibitor) in patients with advanced solid tumors.

METHODS:

This phase 1b, open-label, dose-escalation study (NCT03745989) enrolled adults with histologically/cytologically documented, locally advanced/metastatic solid tumors. MK-8353/selumetinib dose combinations were intended to be investigated in sequence 50/25, 100/50, 150/75, 200/75, 200/100, and 250/100. Each agent was administered orally BID 4 days on/3 days off in repeating cycles every 21 days. Primary objectives were safety and tolerability and to establish preliminary recommended phase 2 doses for combination therapy.

RESULTS:

Thirty patients were enrolled. Median (range) age was 61.5 (26-78) years and 93% had received previous cancer therapy. Among 28 patients in the dose-limiting toxicities [DLT]-evaluable population, 8 experienced DLTs 1/11 (9%) in the MK-8353/selumetinib 100/50-mg dose level experienced a grade 3 DLT (urticaria), and 7/14 (50%) in the 150/75-mg dose level experienced grade 2/3 DLTs (n = 2 each of blurred vision, retinal detachment, vomiting; n = 1 each of diarrhea, macular edema, nausea, retinopathy). The DLT rate in the latter dose level exceeded the prespecified target DLT rate (~30%). Twenty-six patients (87%) experienced treatment-related adverse events (grade 3, 30%; no grade 4/5), most commonly diarrhea (67%), nausea (37%), and acneiform dermatitis (33%). Three patients (10%) experienced treatment-related adverse events leading to treatment discontinuation. Best response was stable disease in 14 patients (n = 10 with MK-8353/selumetinib 150/75 mg).

CONCLUSION:

MK-8353/selumetinib 50/25 mg and 100/50 mg had acceptable safety and tolerability, whereas 150/75 mg was not tolerable. No responses were observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article