Abstract 900P
Background
We aimed to study the effect of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections on patients with head and neck malignancies and evaluate the efficacy of vaccination.
Methods
The Head and Neck cancERs international cOviD-19collabOraTion (HERODOTUS) registry is a multicentre observational study comprised of a retrospective component and a prospective cohort component. Eligibility criteria were the presence of any head and neck cancer (including salivary gland, thyroid, nasal and paranasal cancer) and a COVID-19 diagnosis. Clinical data were extracted from medical records of consecutive patients from November 1, 2019 until September 30, 2022. Associations between demographic or clinical characteristics and outcomes were measured by odds ratios (ORs) with 95% CIs using univariable and multivariable logistic regression; sex, age, smoking status, and HPV status (for oropharynx cancer) were the covariates included in the multivariable analysis. End points include mortality, hospitalization, symptomatic COVID-19 infection, asymptomatic COVID-19 infection, and delay in cancer therapy.
Results
395 COVID-19+ head and neck cancers were identified, out of which, there were 76 deaths. Univariable analyses revealed that age >63 years (OR 3.4, CI 1.9-5.9)); being a current or former smoker (OR: 2, CI: 1.1-2.8), having comorbidities (OR: 2.4, CI: 1.2-5), having a history of COPD (OR: 3.6, CI: 1.7-8), having squamous cell carcinoma (HNSCC) (OR: 4.3, CI: 1.8-10.2), or receiving treatment with chemotherapy and cetuximab (OR: 3.8, CI: 1.4-10.5) were associated with increased risk of death, whereas vaccination was protective (OR: 0.20,CI: 0.11 – 0.34). On multivariable analysis, age>63 yo (OR: 2.3, CI: 1.0-5.2), COPD (OR: 4.9, CI: 1.8-13.8), and chemotherapy with cetuximab (OR: 6.1, CI: 1.9-20) were associated with increased risk of death. Non-vaccinated HNSCC pts had an OR for death of 27.7 (CI: 6.2-122).
Conclusions
This is the largest, to our knowledge, cohort of patients with Head and Neck Cancer and COVID-19. The data show the negative impact of age, COPD and the chemotherapy plus cetuximab regimens on survival while vaccination was protective.
Clinical trial identification
NCT04632173.
Editorial acknowledgement
Legal entity responsible for the study
Hellenic Cooperative Oncology Group.
Funding
Hellenic Cooperative Oncology Group.
Disclosure
A. Psyrri: Financial Interests, Personal, Invited Speaker: MSD, Merck Serono; Financial Interests, Personal, Advisory Board: Pfizer, Sanofi, MSD, AstraZeneca, BMS, LEO, RAKUTEN, eTheRNA immunotherapies, Merck Serono; Financial Interests, Personal and Institutional, Local PI: AstraZeneca, Pfizer, GSK, GENESIS, Incyte, Amgen, Debiopharm, MSD, Jannsen, Lilly, Regeneron, Sanofi, BI, Roche, Peregrine, Oncolytics Biotech; Financial Interests, Coordinating PI: AstraZeneca; Financial Interests, Personal and Institutional, Steering Committee Member: Iovance, Pfizer, Roche; Financial Interests, Institutional, Steering Committee Member: KURA ONCOLOGY; Financial Interests, Steering Committee Member: KURA ONCOLOGY; Financial Interests, Personal and Institutional, Funding: KURA ONCOLOGY, BMS, Roche, DEMO, Amgen, BI, GENESIS, BMS, Pfizer, Oncolytics Biotech; Financial Interests, Institutional, Funding: Merck Serono, Pfizer; Financial Interests, Personal, Other, Educational activity: MEDSCAPE, PrimeOncology; Financial Interests, Institutional, Local PI: Novartis, Replimmune; Non-Financial Interests, Project Lead, Medical Education with honoraria: MEDSCAPE. R. Mesia Nin: Financial Interests, Personal, Advisory Board: Merck, MSD, Bayer, Seattle Genetics, Nanobiotix, Boehringer, Segean; Financial Interests, Personal, Invited Speaker: Merck, MSD, BMS; Non-Financial Interests, Principal Investigator, Clinical Trial PI: BMS; Non-Financial Interests, Principal Investigator, Observational trial PI: Merck. L.F.L. Licitra: Financial Interests, Personal, Advisory Board, for expert opinion in advisory boards: AstraZeneca, Bayer, BMS, Eisai, MSD, Merck–Serono, Boehringer Ingelheim, Hoffmann-La Roche Ltd, Novartis, Roche, Debiopharm International SA, Sobi, Incyte Biosciences Italy srl, Doxa Pharma srl, Amgen, Nanobiotics e GSK.; Financial Interests, Institutional, Research Grant, Funds received by my institution for clinical studies and research activities in which I am involved: AstraZeneca, BMS, Boehringer Ingelheim, Celgene International, Eisai, Exelixis, Debiopharm International SA, Hoffmann-La Roche ltd, IRX Therapeutics, Medpace, Merck–Serono, Merck Healthcare KGaA, MSD, Novartis, Pfizer, Roche, Buran.. All other authors have declared no conflicts of interest.
Resources from the same session
942P - Response to salvage chemotherapy with paclitaxel +/- cetuximab after progression on immune checkpoint inhibitors in platinum-refractory recurrent and/or metastatic squamous cell carcinoma of the head and neck (R/M SCCHN) patients (CeTax study)
Presenter: Ruth Gabriela Herrera Gomez
Session: Poster session 12
944TiP - Randomized phase II study of immune stimulation with pembrolizumab and radiotherapy of recurrent and/or metastatic head and neck squamous cell carcinoma : The IMPORTANCE trial
Presenter: Bálint Tamaskovics
Session: Poster session 12
1089P - Adjuvant nivolumab (NIVO) vs ipilimumab (IPI) in resected stage III/IV melanoma: 7-y results from CheckMate 238
Presenter: Paolo Ascierto
Session: Poster session 12
1090P - Outcome impact of time from complete resection to start of adjuvant immunotherapy in stage III-IV melanoma patients
Presenter: Sergio Martinez Recio
Session: Poster session 12
1092P - Adjuvant treatment with anti-PD-1 in acral melanoma patients: A nationwide study
Presenter: Manja Bloem
Session: Poster session 12
1093P - Neoadjuvant (NeoAd) intratumoral (IT) TAVO-EP (plasmid IL-12 electro gene transfer) in combination with nivolumab (NIVO) for patients (pts) with operable locoregionally advanced melanoma
Presenter: Ahmad Tarhini
Session: Poster session 12
1094P - Relapse free survival (RFS) at 3 years by pathological (path) response to neoadjuvant systemic treatment (NST) in patients (pts) with surgically resectable, high-risk melanoma
Presenter: Elizabeth Burton
Session: Poster session 12
1095P - Associations between baseline biomarkers and 3-year survival in the PRADO trial testing neoadjuvant ipilimumab and nivolumab in stage III melanoma
Presenter: Irene Reijers
Session: Poster session 12