First-in-human study of oleclumab, a potent, selective anti-CD73 monoclonal antibody, alone or in combination with durvalumab in patients with advanced solid tumors.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 02 11 2022
accepted: 19 03 2023
medline: 15 6 2023
pubmed: 5 4 2023
entrez: 4 4 2023
Statut: ppublish

Résumé

CD73 upregulation in tumors leads to local immunosuppression. This phase I, first-in-human study evaluated oleclumab (MEDI9447), an anti-CD73 human IgG1λ monoclonal antibody, alone or with durvalumab in patients with advanced colorectal cancer (CRC), pancreatic ductal adenocarcinoma (PDAC), or epidermal growth factor receptor-mutant non-small-cell lung cancer (NSCLC). Patients received oleclumab 5-40 mg/kg (dose-escalation) or 40 mg/kg (dose-expansion) intravenously every 2 weeks (Q2W), alone (escalation only) or with durvalumab 10 mg/kg intravenously Q2W. 192 patients were enrolled, 66 during escalation and 126 (42 CRC, 42 PDAC, 42 NSCLC) during expansion. No dose-limiting toxicities occurred during escalation. In the monotherapy and combination therapy escalation cohorts, treatment-related adverse events (TRAEs) occurred in 55 and 54%, respectively, the most common being fatigue (17 and 25%). In the CRC, PDAC, and NSCLC expansion cohorts, 60, 57, and 45% of patients had TRAEs, respectively; the most common were fatigue (15%), diarrhea (9%), and rash (7%). Free soluble CD73 and CD73 expression on peripheral T cells and tumor cells showed sustained decreases, accompanied by reduced CD73 enzymatic activity in tumor cells. Objective response rate during escalation was 0%. Response rates in the CRC, PDAC, and NSCLC expansion cohorts were 2.4% (1 complete response [CR]), 4.8% (1 CR, 1 partial response [PR]), and 9.5% (4 PRs), respectively; 6-month progression-free survival rates were 5.4, 13.2, and 16.0%. Oleclumab ± durvalumab had a manageable safety profile, with pharmacodynamic activity reflecting oleclumab's mechanism of action. Evidence of antitumor activity was observed in tumor types that are generally immunotherapy resistant. Clinicaltrials.gov, NCT02503774; date of registration, July 17, 2015.

Sections du résumé

BACKGROUND BACKGROUND
CD73 upregulation in tumors leads to local immunosuppression. This phase I, first-in-human study evaluated oleclumab (MEDI9447), an anti-CD73 human IgG1λ monoclonal antibody, alone or with durvalumab in patients with advanced colorectal cancer (CRC), pancreatic ductal adenocarcinoma (PDAC), or epidermal growth factor receptor-mutant non-small-cell lung cancer (NSCLC).
METHODS METHODS
Patients received oleclumab 5-40 mg/kg (dose-escalation) or 40 mg/kg (dose-expansion) intravenously every 2 weeks (Q2W), alone (escalation only) or with durvalumab 10 mg/kg intravenously Q2W.
RESULTS RESULTS
192 patients were enrolled, 66 during escalation and 126 (42 CRC, 42 PDAC, 42 NSCLC) during expansion. No dose-limiting toxicities occurred during escalation. In the monotherapy and combination therapy escalation cohorts, treatment-related adverse events (TRAEs) occurred in 55 and 54%, respectively, the most common being fatigue (17 and 25%). In the CRC, PDAC, and NSCLC expansion cohorts, 60, 57, and 45% of patients had TRAEs, respectively; the most common were fatigue (15%), diarrhea (9%), and rash (7%). Free soluble CD73 and CD73 expression on peripheral T cells and tumor cells showed sustained decreases, accompanied by reduced CD73 enzymatic activity in tumor cells. Objective response rate during escalation was 0%. Response rates in the CRC, PDAC, and NSCLC expansion cohorts were 2.4% (1 complete response [CR]), 4.8% (1 CR, 1 partial response [PR]), and 9.5% (4 PRs), respectively; 6-month progression-free survival rates were 5.4, 13.2, and 16.0%.
CONCLUSIONS CONCLUSIONS
Oleclumab ± durvalumab had a manageable safety profile, with pharmacodynamic activity reflecting oleclumab's mechanism of action. Evidence of antitumor activity was observed in tumor types that are generally immunotherapy resistant.
CLINICAL TRIAL REGISTRATION BACKGROUND
Clinicaltrials.gov, NCT02503774; date of registration, July 17, 2015.

Identifiants

pubmed: 37016126
doi: 10.1007/s00262-023-03430-6
pii: 10.1007/s00262-023-03430-6
pmc: PMC10264501
doi:

Substances chimiques

durvalumab 28X28X9OKV
Antibodies, Monoclonal 0
Antineoplastic Agents 0

Banques de données

ClinicalTrials.gov
['NCT02503774']

Types de publication

Clinical Trial, Phase I Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2443-2458

Informations de copyright

© 2023. The Author(s).

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Auteurs

Johanna Bendell (J)

Sarah Cannon Research Institute, Nashville, TN, USA. Johanna.bendell@roche.com.
Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Basel, Switzerland. Johanna.bendell@roche.com.

Patricia LoRusso (P)

Yale University Cancer Center, New Haven, CT, USA.

Michael Overman (M)

University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Anne M Noonan (AM)

Ohio State University, Wexner Medical Center, James Comprehensive Cancer Center, Columbus, OH, USA.

Dong-Wan Kim (DW)

Seoul National University Hospital, Seoul, South Korea.

John H Strickler (JH)

Duke University Medical Center, Durham, NC, USA.

Sang-We Kim (SW)

Asan Medical Center, Seoul, South Korea.

Stephen Clarke (S)

Royal North Shore Hospital, St. Leonards, NSW, Australia.

Thomas J George (TJ)

University of Florida Health Cancer Center, Gainesville, FL, USA.

Peter S Grimison (PS)

Chris O'Brien Lifehouse, Camperdown, NSW, Australia.

Minal Barve (M)

Mary Crowley Cancer Research, Dallas, TX, USA.

Manik Amin (M)

Washington University School of Medicine, St. Louis, MO, USA.
Dartmouth-Hitchcock Medical Center, Norris Cotton Cancer Center, Lebanon, NH, USA.

Jayesh Desai (J)

Royal Melbourne Hospital, Parkville, VIC, Australia.

Trisha Wise-Draper (T)

University of Cincinnati Cancer Center, Cincinnati, OH, USA.

Steven Eck (S)

AstraZeneca, Gaithersburg, MD, USA.

Yu Jiang (Y)

AstraZeneca, Gaithersburg, MD, USA.

Anis A Khan (AA)

AstraZeneca, Gaithersburg, MD, USA.

Yuling Wu (Y)

AstraZeneca, Gaithersburg, MD, USA.

Philip Martin (P)

AstraZeneca, Gaithersburg, MD, USA.

Zachary A Cooper (ZA)

AstraZeneca, Gaithersburg, MD, USA.

Nairouz Elgeioushi (N)

AstraZeneca, Gaithersburg, MD, USA.

Nancy Mueller (N)

AstraZeneca, Gaithersburg, MD, USA.

Rakesh Kumar (R)

AstraZeneca, Gaithersburg, MD, USA.

Sandip Pravin Patel (SP)

Moores Cancer Center, University of California San Diego, La Jolla, San Diego, CA, USA.

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Classifications MeSH