Abstract 932P
Background
Extranodal extension on radiology (iENE) is used routinely as an eligibility criterion for surgical treatment. However, studies report widely varying sensitivities, specificities and interobserver correlation.
Methods
We assessed the prognostic power, sensitivity and specificity of iENE in comparison to ENE on pathology (pENE) in a large multinational, multicentre cohort of consecutive HPV+OPC cases in a real-world setting. Outcomes were overall survival (OS) and accuracy.
Results
821 p16+OPC subjects included from 10 centres in 5 countries. 21.3% cass with no iENE were found to have pENE, and 56.8% cases with pENE were misclassified as having no ENE on radiology (ie no iENE). Sensitivity and specificity for iENE were 44.5% (95% CI 37.8 – 51.4 %) and 87.6% (95% CI 84.1-90.6 %) respectively, and varied significantly between centres. Negative predictive value was 75.3% (95%CI 72.3-77.5%). Subgroup analyses showed significantly increased sensitivity and specificity if patients had both CT and MRI: 84.6% (95%CI 65.1- 95.6%, p<0.001) and 94.5% (95%CI 82.3-99.4%, p=0.022) respectively, compared to only CT [47.45% (95% CI 38.86, 56.15) and 78.43% (72.15, 83.87))r] or MRI [18.60% (95% CI 8.39, 33.40, p<0.001) and 96.73 (92.54, 98.93, p<0.001). Specialist radiologists showed better specificities to non-specialists. On multivariable analysis, iENE positivity was not a statistically significant predictor of OS (adjusted hazards ratio (aHR) 1.50 (95%CI 0.97-2.32, p=0.071)) or disease-free survival (aHR1.41, 95CI 0.95-2.09, p=0.089).
Conclusions
In current real-world practice, iENE accuracy was modest, varied widely between centres, and was not independently prognostic of outcomes in HPV+OPC. However, iENE accuracy and prognostic power may be increased significantly by using combined CT and MRI scanning, experienced head and neck radiologists and more inclusive diagnostic criteria. Work is urgently needed to develop and validate consensus diagnostic criteria and protocols to enhance the clinical utility of iENE. Till then, clinicians should be cautious about making treatment decisions based on iENE.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
H. Mehanna.
Funding
Has not received any funding.
Disclosure
H. Mehanna: Financial Interests, Personal, Invited Speaker: MSD, Merck; Financial Interests, Personal, Advisory Board: Merck, Nanobiotix, Seagen, Seattle Genetics; Financial Interests, Personal, Member of Board of Directors: Warwickshire Head Neck Clinic; Financial Interests, Personal, Stocks/Shares: Warwickshire Head Neck Clinic; Financial Interests, Institutional, Research Grant: AstraZeneca; Non-Financial Interests, Leadership Role, Chair of the Head and Neck Cancer International Group: HNCIG; Non-Financial Interests, Other, Research grant Co-investigator: Cancer Research UK; Non-Financial Interests, Other, Research Grant Co-Investigator: European Commission; Non-Financial Interests, Other, Research Grant co-investigator: NIH; Non-Financial Interests, Principal Investigator, Research Grant: NIHR; Non-Financial Interests, Member: ASCO, BACO. C. Henson: Financial Interests, Institutional, Advisory Board: EMD Serono; Non-Financial Interests, Personal, Officer: HNCIG Young Investigators. L. McDowell: Financial Interests, Institutional, Advisory Board: MSD. W. Lydiatt: Financial Interests, Personal, Invited Speaker, honorarium for speaking: Sarah Cannon Cancer Center; Non-Financial Interests, Leadership Role, President elect and President starting May 16, 2024 for one year: American Head and Neck Society; Non-Financial Interests, Leadership Role, Chair of Head and Neck Staging Core groupEditorial Board member: AJCC. S. Yom: Financial Interests, Institutional, Research Grant: Bristol Myers Squibb, EMD Serono, Nanobiotix; Financial Interests, Personal, Royalties: Springer, UpToDate; Financial Interests, Personal, Speaker’s Bureau: Elsevier, ASTRO. M. Oliva Bernal: Financial Interests, Personal, Invited Speaker: Merck, MSD, BMS; Financial Interests, Personal, Advisory Board: Merck, MSD; Financial Interests, Personal, Writing Engagement: MSD; Financial Interests, Personal, Invited Speaker, Teaching activities: MSD, Merck; Financial Interests, Personal, Other, IDMC: Transgene; Financial Interests, Personal and Institutional, Funding: Roche; Financial Interests, Institutional, Local PI: ALX Oncology, MSD, ISA Therapeutics BV, Roche, Ayala Therapeutics, Abbvie, Bayer, Boehringer Ingelheim, Merck, Debiopharm, Seagen, Gilead, Beigene, NYKODE; Financial Interests, Institutional, Funding: GSK; Non-Financial Interests, Institutional, Product Samples: Roche. R. Leemans: Financial Interests, Personal, Advisory Board: MSD. All other authors have declared no conflicts of interest.
Resources from the same session
938TiP - Phase II TROPHY-IO-HN study of pembrolizumab ±sacituzumab govitecan in first-line recurrent /metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) patients
Presenter: Amanda Psyrri
Session: Poster session 03
941TiP - A phase I/IIa, open-label, dose-finding trial to evaluate safety, immunogenicity, and anti-tumour activity of VB10.16 in combination with pembrolizumab in patients with unresectable recurrent or metastatic HPV16-positive head and neck squamous cell carcinoma (R/M HNSCC)
Presenter: Saira Khalique
Session: Poster session 03
942TiP - A randomized controlled clinical trial of neoadjuvant immunochemotherapy vs up-front surgery in patients with locally advanced resectable oral squamous cell carcinoma (Tophill trial)
Presenter: Laiping Zhong
Session: Poster session 03
Resources:
Abstract
945TiP - JADE: A phase (ph) III study to evaluate dostarlimab vs placebo (PBO) as sequential therapy after chemoradiation (CRT) in patients (pts) with locally advanced unresected head and neck squamous cell carcinoma (LA-HNSCC)
Presenter: Jean-Pascal Machiels
Session: Poster session 03
1002P - A phase Ia study of the myeloid-derived suppressor cell modulator HF1K16 in refractory and metastatic cancer patients: Preliminary efficacy and safety
Presenter: Ruofan Huang
Session: Poster session 03
1003P - A first-in-human (FIH) phase I study of IPH5301, an anti-CD73 monoclonal antibody (mAb), in patients with advanced solid tumors (AST) (CHANCES, NCT05143970)
Presenter: Mathilde Beaufils
Session: Poster session 03