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Amivantamab Monotherapy in Chemorefractory RAS/BRAF Wild-Type Metastatic Colorectal Cancer: Results From OrigAMI-1, an Open-Label, Phase Ib/II Study

Authors
 Oberstein, Paul E.  ;  Hecht, J. Randolph  ;  Raghav, Kanwal  ;  Pietrantonio, Filippo  ;  Arnold, Dirk  ;  Moreno, Victor  ;  Van Cutsem, Eric  ;  Malik, Rozita Abdul  ;  Hong, Yong Sang  ;  Lee, Myung Ah  ;  Yu-Li Su, Harvey  ;  Lee, Jeeyun  ;  Chandana, Sreenivasa  ;  Cruz-Correa, Marcia  ;  Yuan, Ying  ;  Ahmad, Azura  ;  Lai, Kuan-Ming  ;  Hsu, Hung-Chih  ;  Chen, Eric Xueyu  ;  Elez, Elena  ;  Lin, Chia-Chi  ;  Lopez, Carlos  ;  Prenen, Hans  ;  Rosello-Keranen, Susana  ;  Velez, Hector  ;  Yeh, Yu-Min  ;  Heinemann, Volker  ;  Eng, Cathy  ;  Beom, Seung-Hoon  ;  Tejpar, Sabine  ;  Chowdhury, Sanjib  ;  Lyu, Xuesong  ;  Kamat, Medha  ;  Curtin, Joshua C.  ;  Patel, Bharvin  ;  Xie, John  ;  Bhattacharya, Rianka  ;  Schnepp, Robert W.  ;  Yilmaz, Emrullah  ;  Iwasawa, Ryota  ;  Daksh, Mahesh  ;  Lorenzini, Patricia  ;  Thayu, Meena  ;  Baig, Mahadi  ;  Kim, Han Sang  ;  Han, Sae-Won 
Citation
 JOURNAL OF CLINICAL ONCOLOGY, Vol.44(17) : 1624-1634, 2026-06 
Journal Title
JOURNAL OF CLINICAL ONCOLOGY
ISSN
 0732-183X 
Issue Date
2026-06
MeSH
Adult ; Aged ; Aged, 80 and over ; Antibodies, Bispecific* / adverse effects ; Antibodies, Bispecific* / therapeutic use ; Antineoplastic Agents, Immunological* / adverse effects ; Antineoplastic Agents, Immunological* / therapeutic use ; Colorectal Neoplasms* / drug therapy ; Colorectal Neoplasms* / genetics ; Colorectal Neoplasms* / pathology ; Female ; Humans ; Male ; Middle Aged ; Progression-Free Survival ; Proto-Oncogene Proteins B-raf / genetics
Abstract
PURPOSEAmivantamab, an EGFR-MET bispecific antibody with immune cell-directing activity, is approved in non-small cell lung cancer (NSCLC). Effective treatments are limited for chemorefractory metastatic colorectal cancer (mCRC).METHODSOrigAMI-1 (ClinicalTrials.gov identifier: NCT05379595) is a phase Ib/II study evaluating amivantamab monotherapy in chemorefractory (2-3 prior lines) mCRC. Participants had centrally confirmed RAS/BRAF/EGFR ectodomain wild-type status, without ERBB2/HER2 amplification. Participants with left-sided mCRC without (cohort A) or with (cohort B) prior anti-EGFR antibody treatment, or right-sided mCRC (cohort C) regardless of prior anti-EGFR treatment, received intravenous amivantamab 1,050 mg (1,400 mg for >= 80 kg) once every 2 weeks. The primary end point was objective response rate (ORR) per RECIST v1.1.RESULTSBy October 31, 2024, 94 participants received amivantamab monotherapy (median follow-up, 11.9 months). The median age was 60 years, and 65% of participants were male, with a median of 2 prior lines (94%, prior bevacizumab). In left-sided cohorts, the ORR was 29% (5 of 17) in cohort A and 19% (10 of 54) in cohort B; the median duration of response (DoR) was 9.0 months and 6.1 months, and the median progression-free survival (PFS) was 5.7 months and 4.6 months, respectively. In the right-sided cohort, the ORR was 22% (10 of 23; 43% had prior anti-EGFR), the median DoR was 9.8 months, and the median PFS was 3.7 months. Most frequent treatment-related grade >= 3 adverse events (AEs) were rash (7%), dermatitis acneiform (4%), and hypoalbuminemia (4%). One participant discontinued amivantamab because of a treatment-related AE.CONCLUSIONAmivantamab monotherapy demonstrated promising, durable antitumor activity in chemorefractory mCRC, regardless of prior anti-EGFR therapy and the primary tumor location. The amivantamab safety profile in mCRC is consistent with experience in NSCLC. Amivantamab plus chemotherapy is currently being explored in two phase III studies in first-line and second-line mCRCs.
Full Text
https://ascopubs.org/doi/10.1200/JCO-25-02187
DOI
10.1200/JCO-25-02187
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Han Sang(김한상) ORCID logo https://orcid.org/0000-0002-6504-9927
Beom, Seung Hoon(범승훈) ORCID logo https://orcid.org/0000-0001-7036-3753
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/212960
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