A phase 1b study of the Notch inhibitor crenigacestat (LY3039478) in combination with other anticancer target agents (taladegib, LY3023414, or abemaciclib) in patients with advanced or metastatic solid tumors
- PMID: 33686452
- DOI: 10.1007/s10637-021-01094-6
A phase 1b study of the Notch inhibitor crenigacestat (LY3039478) in combination with other anticancer target agents (taladegib, LY3023414, or abemaciclib) in patients with advanced or metastatic solid tumors
Abstract
Notch signaling plays an important role in development and tissue homeostasis. Deregulation of Notch signaling has been implicated in multiple malignancies. Crenigacestat (LY3039478), a potent Notch inhibitor, decreases Notch signaling and its downstream biologic effects. I6F-MC-JJCD was a multicenter, nonrandomized, open-label, Phase 1b study with 5 separate, parallel dose-escalations in patients with advanced or metastatic cancer from a variety of solid tumors, followed by a dose-confirmation phase in prespecified tumor types. This manuscript reports on 3 of 5 groups. The primary objective was to determine the recommended Phase 2 dose of crenigacestat in combination with other anticancer agents (taladegib, LY3023414 [dual inhibitor of phosphoinositide 3-kinase; mechanistic target of rapamycin], or abemaciclib). Secondary objectives included evaluation of safety, tolerability, efficacy, and pharmacokinetics. Patients (N = 63) received treatment between November 2016 and July 2019. Dose-limiting toxicities occurred in 12 patients, mostly gastrointestinal (diarrhea, nausea, vomiting). The maximum-tolerated dose of crenigacestat was 25 mg in Part B (LY3023414), 50 mg in Part C (abemaciclib), and not established in Part A (taladegib) due to toxicities. Patients had at least 1 adverse event (AE) and 75.0-82.6% were ≥ Grade 3 all-causality AEs. No patient had complete or partial response. Disease control rates were 18.8% (Part B) and 26.1% (Part C). The study was terminated before dose confirmation cohorts were triggered. This study demonstrated that crenigacestat combined with different anticancer agents (taladegib, LY3023414, or abemaciclib) was poorly tolerated, leading to lowered dosing and disappointing clinical activity in patients with advanced or metastatic solid tumors. NCT02784795 and date of registration: May 27, 2016.
Keywords: Abemaciclib; Crenigacestat; LY3039478; Metastatic cancer; Notch inhibition; Phase 1.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Similar articles
-
A phase 1b study of crenigacestat (LY3039478) in combination with gemcitabine and cisplatin or gemcitabine and carboplatin in patients with advanced or metastatic solid tumors.Cancer Chemother Pharmacol. 2022 Oct;90(4):335-344. doi: 10.1007/s00280-022-04461-z. Epub 2022 Aug 28. Cancer Chemother Pharmacol. 2022. PMID: 36030462 Clinical Trial.
-
A phase 1 study of crenigacestat (LY3039478), the Notch inhibitor, in Japanese patients with advanced solid tumors.Invest New Drugs. 2021 Apr;39(2):469-476. doi: 10.1007/s10637-020-01001-5. Epub 2020 Sep 16. Invest New Drugs. 2021. PMID: 32939607 Free PMC article. Clinical Trial.
-
Phase 1 study of 2 high dose intensity schedules of the pan-Notch inhibitor crenigacestat (LY3039478) in combination with prednisone in patients with advanced or metastatic cancer.Invest New Drugs. 2021 Feb;39(1):193-201. doi: 10.1007/s10637-020-00944-z. Epub 2020 Sep 11. Invest New Drugs. 2021. PMID: 32915419 Clinical Trial.
-
First-in-human study of LY3039478, an oral Notch signaling inhibitor in advanced or metastatic cancer.Ann Oncol. 2018 Sep 1;29(9):1911-1917. doi: 10.1093/annonc/mdy244. Ann Oncol. 2018. PMID: 30060061 Clinical Trial.
-
Abemaciclib: The Newest CDK4/6 Inhibitor for the Treatment of Breast Cancer.Ann Pharmacother. 2019 Feb;53(2):178-185. doi: 10.1177/1060028018795146. Epub 2018 Aug 13. Ann Pharmacother. 2019. PMID: 30099886 Review.
Cited by
-
CDK4/6 Inhibitors in Pancreatobiliary Cancers: Opportunities and Challenges.Cancers (Basel). 2023 Feb 3;15(3):968. doi: 10.3390/cancers15030968. Cancers (Basel). 2023. PMID: 36765923 Free PMC article. Review.
-
Concomitant activation of GLI1 and Notch1 contributes to racial disparity of human triple negative breast cancer progression.Elife. 2021 Dec 10;10:e70729. doi: 10.7554/eLife.70729. Elife. 2021. PMID: 34889737 Free PMC article.
-
Notch Signalling in Breast Development and Cancer.Front Cell Dev Biol. 2021 Jul 6;9:692173. doi: 10.3389/fcell.2021.692173. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34295896 Free PMC article. Review.
-
Development and Evolution of DNA-Dependent Protein Kinase Inhibitors toward Cancer Therapy.Int J Mol Sci. 2022 Apr 12;23(8):4264. doi: 10.3390/ijms23084264. Int J Mol Sci. 2022. PMID: 35457081 Free PMC article. Review.
-
Molecular pathways and targeted therapies in head and neck cancers pathogenesis.Front Oncol. 2024 Jun 17;14:1373821. doi: 10.3389/fonc.2024.1373821. eCollection 2024. Front Oncol. 2024. PMID: 38952548 Free PMC article. Review.
References
-
- Artavanis-Tsakonas S, Rand MD, Lake RJ (1999) Notch signaling: cell fate control and signal integration in development. Science. 284:770–776. https://doi.org/10.1126/science.284.5415.770 - DOI - PubMed
-
- Allenspach EJ, Maillard I, Aster JC, Pear WS (2002) Notch signaling in cancer. Cancer Biol Ther 1:466–476. https://doi.org/10.4161/cbt.1.5.159 - DOI - PubMed
-
- Takebe N, Miele L, Harris PJ et al (2015) Targeting Notch, Hedgehog, and Wnt pathways in cancer stem cells: clinical update. Nat Rev Clin Oncol 12:445–464. https://doi.org/10.1016/j.pharmthera.2013.09.005 - DOI - PubMed - PMC
-
- Wang Z, Li Y, Sarkar FH (2010) Notch signaling proteins: legitimate targets for cancer therapy. Curr Protein Pept Sci 11:398e408. https://doi.org/10.2174/138920310791824039 - DOI
-
- Koch U, Radtke F (2007) Notch and cancer: a double-edged sword. Cell Mol Life Sci 64:2746–2762. https://doi.org/10.1007/s00018-007-7164-1 - DOI - PubMed
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources
Other Literature Sources
