Abstract 907P
Background
Adenoid cystic carcinoma (ACC) is characterized by multiple relapses and a poor prognosis. It is commonly considered a radioresistant tumor, indeed particle radiotherapy is especially indicated in ACC. Recently, ACC was stratified in two clusters with a different prognosis, ACC type I and II, according to distinct molecular features i.e. NOTCH activating mutation and TP63 upregulation, respectively. We aimed to disclose molecular profiles predictive of radiosensitivity or radioresistance features.
Methods
The study cohort comprised 54 patients with ACC of salivary gland origin, treated with surgery plus photon beam radiotherapy (R) or R alone. A survey in the literature yielded a list of 15 signatures including pan-cancer or different tumor-specific models (e.g. head and neck; breast cancer; glioblastoma; prostate cancer) with a total of 141 genes. The expression levels of these genes were retrieved and signatures scores were imputed following the methods described in the original papers. Log2-trasformed transcripts per million mapped reads values were retrieved from Ferrarotto et al. [PMC7854509]. Clinical and follow-up data were updated at 31st December 2022; overall survival (OS) as endpoint was estimated with the Kaplan-Meier method.
Results
Only the signatures developed on breast cancer gene-expression datasets among those investigated were able to stratify ACC patients; in particular, we focused on an immune-radiosensitivity signature [PMC8984882] able to reach HR=7.59, 95%CI 3.19-18.09, p=1e-07. The predicted radiosensitivity of this signature was significantly associated with ACC type II and lack of NOTCH mutations.
Conclusions
Molecular profile of ACC type II is significantly associated with an intrinsic radiosensitivity. The association of ACC radiosensitivity to breast cancer signatures warrants further research on the biology behind ACC and its molecular similarities.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
932P - Survival in patients with relapsed/metastatic head and neck squamous cell carcinoma (HNSCC) treated with pembrolizumab or cetuximab-based therapy: A real-worlddata study with the TriNetX platform
Presenter: Lisardo Ugidos De La Varga
Session: Poster session 12
934P - Antitumor activity and safety profile of camrelizumab plus docetaxel, cisplatin, and capecitabine for induction therapy in advanced stage hypopharyngeal carcinoma
Presenter: Hongli Gong
Session: Poster session 12
938P - Nivolumab (nivo) in recurrent and/or metastatic squamous cell carcinoma of head and neck (R/M SCCHN): real-world effectiveness, quality of life (QoL) of patients and their caregivers in France (ProNiHN study)
Presenter: Christophe Le Tourneau
Session: Poster session 12
939P - Efficacy and safety of a novel anti-EGFR ADC MRG003 in recurrent or metastatic squamous cell carcinoma of the head and neck patients
Presenter: Liqiong Xue
Session: Poster session 12
940P - Salvage chemotherapy after progression on nivolumab in patients with squamous cell carcinoma of the head and neck included in the phase II TOPNIVO trial
Presenter: Khalil Saleh
Session: Poster session 12
941P - Risk factors for progressive disease after immune checkpoint inhibitors (ICIs) in advanced head and neck squamous cell carcinoma (HNSCC): Who might not be candidate for ICI?
Presenter: Seo Yoon Jang
Session: Poster session 12