Abstract 573P
Background
M9140 is an anti-CEACAM5 ADC that selectively delivers a cytotoxic topoisomerase 1 inhibitor payload (exatecan). Preliminary data from the dose escalation part of the ongoing trial (NCT05464030) showed encouraging antitumor activity and a manageable safety profile of M9140 in heavily pretreated patients with mCRC. Herein, longer follow-up data and biomarker analysis will be presented.
Methods
Part 1 of this Phase 1 trial investigated the safety and preliminary clinical activity of M9140 monotherapy (Q3W; IV) in patients with 3L+ mCRC. In addition to CEACAM5 IHC from archival tissue, patient records/archival tissue were assessed for KRAS, NRAS, and BRAF mutations.
Results
As of April 2024, 40 patients were treated across 7 dose levels (DLs) (0.6–3.2 mg/kg; 3 patients with primary G-CSF prophylaxis at DL 3.2 mg/kg). Median treatment duration was 16.4 weeks (range: 1.7–47). Overall, 4 (10%) patients achieved partial response (PR; including 1 unconfirmed PR) at DLs ≥2.4 mg/kg, and 0 at <2.4 mg/kg. Stable disease was observed in 22 (55.0%) patients, progressive disease in 7 (17.5%) patients, and the best overall response was not evaluable in 7 (17.5%) patients. Progression-free survival was higher for patients treated with M9140 ≥2.4 mg/kg vs <2.4 mg/kg (6.7 [95% CI 5.0, 8.8] vs 2.1 [95% CI 1.2, ne] months). Eleven (27.5%) patients continue on treatment. Overall, 7 patients experienced dose-limiting toxicities; the majority were hematological adverse events at DLs 3.0 and 3.2 mg/kg (most self-resolved); 1 patient (at 2.8 mg/kg) had a Grade 5 sepsis. No events of interstitial lung disease or ocular toxicity were observed. Updated data with a longer follow-up (data cutoff: early August) will be presented at the congress. The association of M9140 activity with KRAS, NRAS, BRAF mutation status and CEACAM5 levels will also be presented.
Conclusions
With continued follow-up, M9140 continues to exhibit a manageable and predictable safety profile. Encouraging antitumor activity was observed at DLs ≥2.4 mg/kg. DLs 2.4 and 2.8 mg/kg, identified as the recommended doses for expansion, are currently being evaluated in the randomized dose optimization part of the study.
Clinical trial identification
NCT05464030.
Editorial acknowledgement
Medical writing assistance was provided by Gaurav Vijay Jadhav of Merck Specialities Pvt. Ltd, Bangalore, India, an affiliate of Merck KGaA.
Legal entity responsible for the study
Merck.
Funding
The study was sponsored by Merck (CrossRef Funder ID: 10.13039/100009945).
Disclosure
V. Boni: Financial Interests, Institutional, Full or part-time Employment: Quironsalud, Next Oncology; Financial Interests, Institutional, Stocks or ownership: 1TRIALSP; Financial Interests, Institutional, Royalties: Loxo, IDEAYA Biosciences, Puma Biotechnology, Amunix, Guidepoint Global, MSD Oncology, Janssen Oncology, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA; Financial Interests, Institutional, Advisory Role: OncoArt, Guidepoint Global, Janssen Research & Development, Lilly, Nanobiotix, Novartis, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA; Financial Interests, Institutional, Research Funding: Sanofi, Seagen, Loxo, Novartis, CytomX Therapeutics, Puma Biotechnology, Kura Oncology, Tesaro, Roche/Genentech, Bristol-Myers Squibb, Menarini, Synthon, Janssen Oncology, Merck Healthcare KGaA, Darmstadt, Germany, Lilly, Merus, Pfizer, Bayer, Incyte, Abb; Financial Interests, Personal and Institutional, Other, Travel, Accommodations, Expenses: START, Bayer; Financial Interests, Institutional, Speaker’s Bureau: Solti, Lilly, TACTICS, MSD, TACTICS;. S. Kopetz: Financial Interests, Institutional, Advisory Role: Genentech, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA, MSD, Holy Stone Healthcare, Novartis, Lilly, AstraZeneca/MedImmune, Bayer Health, Redx Pharma, Ipsen, HalioDx, Lutris, Jacobio, Pfizer, Repare Th; Financial Interests, Institutional, Stocks or ownership: Lutris, Iylon, Frontier Medicines, Xilis, and Navire; Financial Interests, Institutional, Research Funding: Sanofi, Biocartis, Guardant Health, Array BioPharma, Genentech/Roche, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA, MedImmune, Novartis, Amgen, Lilly, and Daiichi Sankyo. K. Kato: Financial Interests, Institutional, Advisory Role: Ono Pharmaceutical, BeiGene, MSD, Oncolys BioPharma, Bayer; Financial Interests, Institutional, Royalties: Lilly, Bristol-Myers Squibb, Ono Pharmaceutical; Financial Interests, Institutional, Research Funding: Ono Pharmaceutical, Shionogi, MSD Oncology, BeiGene, Chugai Pharma, Bayer, AstraZeneca, Taiho Pharmaceutical; Financial Interests, Institutional, Speaker’s Bureau: Ono Pharmaceutical, Bristol-Myers Squibb Japan, MSD. K. Raghav: Financial Interests, Institutional, Advisory Role: Bayer, Eisai, MSD, Daiichi Sankyo, AstraZeneca, Seagen; Financial Interests, Institutional, Royalties: Bayer, Eisai, MSD, Daiichi Sankyo, AstraZeneca, Seagen; Financial Interests, Institutional, Research Funding: Bayer, Roche/Genentech, Guardant Health, HiberCell, Merck Healthcare KGaA, Darmstadt, Germany, Abbvie, Eisai, Xencor, Innovent Biologics, Janssen, UCB, Daiichi Sankyo, AstraZeneca. M. Vieito: Financial Interests, Personal, Invited Speaker: NOVOCURE; Financial Interests, Personal, Other, Steering committee member: BMS; Non-Financial Interests, Principal Investigator: Roche, BMS, Taiho, Hutchinson Pharma, Novartis, Mundipharma, Enterome, Debiopharm. A.G. Pallis: Financial Interests, Institutional, Full or part-time Employment: Merck Santé S.A.S., Lyon, France, an affiliate of Merck KGaA. C. Habermehl: Financial Interests, Institutional, Full or part-time Employment: Merck Healthcare KGaA, Darmstadt, Germany. I.I. Rodriguez Rivera: Financial Interests, Institutional, Full or part-time Employment: Next Oncology, Texas Oncology; Consulting and advisory role: Syneos Health, Cardinal Health, Werewolf Therapeutics, Telix Pharmaceuticals; Financial Interests, Institutional, Research Funding: 1st Biotherapeutics, Amgen, Apollo Therapeutics, BeiGene, Boundless Bio, Deciphera Pharmaceuticals, EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA, Flare Therapeutics, Kumquat Biosciences Inc, Navire Phar.
Resources from the same session
479P - The candidate novel markers PIV and PILE score to predict survival outcomes and therapeutic response in patients with primary central nervous system lymphoma
Presenter: Ling Duan
Session: Poster session 16
Resources:
Abstract
480P - Clinical utility of ctDNA detection by NGS for diagnosis of CNS lymphoma
Presenter: Ana Jiménez-Ubieto
Session: Poster session 16
481P - Integrating GWAS and transcriptomics prioritizes drug targets for meningioma
Presenter: Wan-Zhe Liao
Session: Poster session 16
482P - The prognostic impact of CDKN2A/B heterozygous deletions in meningioma: Insights of a multicenter analysis
Presenter: Franziska Ippen
Session: Poster session 16
483P - The use of steroids associated with PD1/PDL-1 blockage in patients with brain metastasis: A systematic review and meta-analysis
Presenter: Francisco Cezar Moraes
Session: Poster session 16
484P - EGFR amplification is the potential driver gene that accelerates brain metastases in NSCLC patients
Presenter: Hainan Yang
Session: Poster session 16
485P - A spatio-temporal evolution mathematical model of glioma growth: The influence of cellular and nutrient interactions on the tumor microenvironment
Presenter: Kalysta Borges
Session: Poster session 16
486P - Effects of a BBB-penetrating oligonucleotide drug, RBD8088, in mouse models of human glioblastoma
Presenter: Julia Grönros
Session: Poster session 16
487P - 3D-bioprinted co-cultures of glioblastoma and mesenchymal cells indicate a role for perivascular niche cells in shaping the chemotactic tumour microenvironment
Presenter: Radosław Zagożdżon
Session: Poster session 16
488P - ITGA2 promotes glioma cell stemness and progression by activating the AKT pathway
Presenter: Lihui Wang
Session: Poster session 16