Combination Treatment of Intratumoral Vidutolimod, Radiosurgery, Nivolumab, and Ipilimumab for Microsatellite Stable Colorectal Carcinoma With Liver Metastases.
Humans
Male
Adult
Middle Aged
Aged
Female
Ipilimumab
/ therapeutic use
Nivolumab
/ therapeutic use
Antineoplastic Agents, Immunological
/ adverse effects
Radiosurgery
/ adverse effects
Colorectal Neoplasms
/ therapy
Colonic Neoplasms
/ drug therapy
Rectal Neoplasms
/ drug therapy
Liver Neoplasms
/ genetics
Microsatellite Repeats
Immunotherapy
Intratumoral injection
Metastatic colorectal cancer
Radiotherapy
Toll-like receptor 9 agonist
Journal
Clinical colorectal cancer
ISSN: 1938-0674
Titre abrégé: Clin Colorectal Cancer
Pays: United States
ID NLM: 101120693
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
received:
09
07
2023
revised:
06
08
2023
accepted:
07
08
2023
medline:
4
12
2023
pubmed:
2
9
2023
entrez:
1
9
2023
Statut:
ppublish
Résumé
Microsatellite stable metastatic colorectal cancer (MSS mCRC) is largely refractory to immune checkpoint inhibition. We hypothesized that a combination of intratumoral TLR9 agonist, radiosurgery and dual PD-1 and CTLA-4 blockade would induce a local focus of immune stimulation, evoking a systemic immune response. In this phase I single-institution study, patients with MSS mCRC were treated with a priming dose of s.c vidutolimod, 3 intratumoral injections of vidutolimod and radiosurgery, combined with nivolumab and ipilimumab. Cytokine levels were measured at baseline and at 7 (± 2) weeks. Patients were accrued to 4 consecutive cohorts: (1) Safety run-in without radiosurgery, (2) Radiosurgery prior to intratumoral therapy, (3) Radiosurgery prior to intratumoral therapy with a condensed timeline, and (4) Radiosurgery to extrahepatic lesion following completion of intratumoral therapy. A total of 19 patients were accrued. Median age was 59 years (range 40-71), 68% were male, median number of previous systemic treatments was 3 (range 2-5). None of the patients responded, aside from 1 patient, attributed to high tumor mutational burden. Grade 3 liver toxicity was reported in 0%, 0%, 75%, and 17% in cohorts 1 to 4, respectively. Systemic levels of CXCL10 and IL-10 increased, with a median of 407 versus 78 pg/mL (P = .01), and 66 versus 40 pg/mL (P = .03), respectively. The combination of intratumoral vidutolimod, radiosurgery, nivolumab and ipilimumab was not found to be efficacious in MSS mCRC with liver metastases. The juxtaposition of liver irradiation and intratumoral vidutolimod injection was associated with high hepatic toxicity.
Identifiants
pubmed: 37657954
pii: S1533-0028(23)00077-4
doi: 10.1016/j.clcc.2023.08.004
pii:
doi:
Substances chimiques
Ipilimumab
0
Nivolumab
31YO63LBSN
Antineoplastic Agents, Immunological
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
442-449.e1Informations de copyright
Copyright © 2023 Elsevier Inc. All rights reserved.