Nivolumab and ipilimumab in combination with radiotherapy in patients with high-risk locally advanced squamous cell carcinoma of the head and neck.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
08 2023
Historique:
accepted: 16 07 2023
medline: 7 8 2023
pubmed: 4 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

The combination of nivolumab and ipilimumab has been approved for the treatment of multiple solid tumors. This was a phase I study investigating definitive radioimmunotherapy (RIT) with nivolumab and ipilimumab for the treatment of locally advanced (LA) squamous cell carcinoma of the head and neck (SCCHN). Patients with newly diagnosed, stage IVA-IVB SCCHN eligible for cisplatin-based chemotherapy received nivolumab (3 mg/kg every 2 weeks for a total of 17 doses) and ipilimumab (1 mg/kg every 6 weeks for a total of 6 doses) starting 2 weeks prior to radiotherapy. The primary endpoint was safety of definitive RIT. Secondary endpoints included progression-free survival (PFS) and overall survival (OS). Exploratory endpoints included the association of baseline programmed death-ligand 1 (PD-L1) expression as well as on-treatment changes in immune bias with treatment outcomes. Twenty-four patients were enrolled. With a median follow-up of 36.1 months, grade 3 or higher treatment-related adverse events were reported in 21 individuals (88%); 5 individuals developed in-field soft tissue ulceration during consolidation immunotherapy, resulting in one fatality. The 3-year PFS and OS rates were 74% (95% CI 58% to 94%) and 96% (95% CI 88% to 100%), respectively. PD-L1 combined positive score (CPS) did not correlate with death or disease progression. Decreases in extracellular vesicle PD-L1 within the concurrent RIT phase were associated with prolonged PFS (p=0.006). Also, interval decreases in circulating interleukin (IL)4, IL9, IL12, and IL17a during concurrent RIT were associated with subsequent ulceration. Definitive RIT with nivolumab and ipilimumab has sufficient clinical activity to support further development. Early changes in circulating biomarkers appear able to predict treatment outcomes as well as ensuing in-field soft tissue ulceration. NCT03162731.

Sections du résumé

BACKGROUND
The combination of nivolumab and ipilimumab has been approved for the treatment of multiple solid tumors. This was a phase I study investigating definitive radioimmunotherapy (RIT) with nivolumab and ipilimumab for the treatment of locally advanced (LA) squamous cell carcinoma of the head and neck (SCCHN).
METHODS
Patients with newly diagnosed, stage IVA-IVB SCCHN eligible for cisplatin-based chemotherapy received nivolumab (3 mg/kg every 2 weeks for a total of 17 doses) and ipilimumab (1 mg/kg every 6 weeks for a total of 6 doses) starting 2 weeks prior to radiotherapy. The primary endpoint was safety of definitive RIT. Secondary endpoints included progression-free survival (PFS) and overall survival (OS). Exploratory endpoints included the association of baseline programmed death-ligand 1 (PD-L1) expression as well as on-treatment changes in immune bias with treatment outcomes.
RESULTS
Twenty-four patients were enrolled. With a median follow-up of 36.1 months, grade 3 or higher treatment-related adverse events were reported in 21 individuals (88%); 5 individuals developed in-field soft tissue ulceration during consolidation immunotherapy, resulting in one fatality. The 3-year PFS and OS rates were 74% (95% CI 58% to 94%) and 96% (95% CI 88% to 100%), respectively. PD-L1 combined positive score (CPS) did not correlate with death or disease progression. Decreases in extracellular vesicle PD-L1 within the concurrent RIT phase were associated with prolonged PFS (p=0.006). Also, interval decreases in circulating interleukin (IL)4, IL9, IL12, and IL17a during concurrent RIT were associated with subsequent ulceration.
CONCLUSIONS
Definitive RIT with nivolumab and ipilimumab has sufficient clinical activity to support further development. Early changes in circulating biomarkers appear able to predict treatment outcomes as well as ensuing in-field soft tissue ulceration.
TRIAL REGISTRATION NUMBER
NCT03162731.

Identifiants

pubmed: 37536941
pii: jitc-2023-007141
doi: 10.1136/jitc-2023-007141
pmc: PMC10401226
pii:
doi:

Substances chimiques

Nivolumab 31YO63LBSN
Ipilimumab 0
B7-H1 Antigen 0

Banques de données

ClinicalTrials.gov
['NCT03162731']

Types de publication

Clinical Trial, Phase I Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : P30 CA056036
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Jennifer M Johnson (JM)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA Jennifer.M.Johnson@Jefferson.edu.
Department of Otolaryngology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Ioannis A Vathiotis (IA)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Larry A Harshyne (LA)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Department of Cancer Biology, Thomas Jefferson University, Philadelphia, PA, USA.

Ayesha Ali (A)

Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Voichita Bar Ad (V)

Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Rita Axelrod (R)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Emily Lorber (E)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Joseph Curry (J)

Department of Otolaryngology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

David M Cognetti (DM)

Department of Otolaryngology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Adam J Luginbuhl (AJ)

Department of Otolaryngology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Madalina Tuluc (M)

Department of Pathology, Anatomy, and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Scott Keith (S)

Department of Pharmacology, Physiology, and Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Mỹ G Mahoney (MG)

Department of Otolaryngology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Department of Dermatology and Cuaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Athanassios Argiris (A)

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

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