Abstract 933P
Background
Limited real-world data exists on treatment patterns and outcomes in R/M HNC pts receiving anti-PD-1 immunotherapy (IT). This study provides insights into contemporary IT use and sequencing. Preliminary results from five centers in four European countries (Italy, Poland, Portugal, Slovenia) are presented.
Methods
A retrospective federated analysis of R/M HNC pts who received IT between March 2017 and May 2022 was conducted. Data were analyzed at each center using a common R script. Overall survival (OS) and real-world progression-free survival (rwPFS) were calculated from IT start. Lines of systemic therapy (line) included concomitant chemotherapy (ChT) used with radiotherapy (CRT).
Results
A total of 224 pts with a median age of 58–67 yrs across countries were included. 43.8% of pts had metastatic disease as opposed to locoregional only at IT start, 64.7% had platinum refractory disease, and 19.2% were tested for PD-L1 expression. 9.8% of pts began their treatment with IT, whereas most pts. received anti-PD-1 after previous CRT or as a 2nd line (pembrolizumab 10.0%, pembrolizumab+ChT 4.4%, nivolumab 85.6%). In the first line, the most common systemic treatments beside platinum-based CRT (39.3%) were platinum-containing combination ChT without cetuximab (37.5%) and ChT+cetuximab (12.0%). The maximum number of lines in any patient was 10 and nivolumab was the most used agent overall (25.6%) followed by non-platinum monochemotherapy (21.4.%). Median overall survival from anti-PD-1 initiation across countries was 5.9–13.6 months (ms), and the median rwPFS ranged from 2.8–4.8 ms. The overall occurrence of irAEs ranged from 18.3–81.3% across countries, with the most common irAEs being gastrointestinal (25.8%) and endocrinal disorders (17.9%). There were 57.3% grade 2, 6.6% grade 3 and no grade 4 or 5 irAEs.
Conclusions
This real-world study across four European countries shows variable IT utilization and outcomes, irAEs occurrence, and treatment patterns in R/M HNC. Further research is needed to optimize IT use, considering pts characteristics and treatment-related factors.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
DIGICORE research network.
Disclosure
A. Kovac: Financial Interests, Personal, Writing Engagement: Novartis; Financial Interests, Personal, Invited Speaker: Ewopharma; Financial Interests, Personal, Other, Travel, accommodation, expenses: MSD; Non-Financial Interests, Member: ASCO, ESO. C. Vieira: Other, Personal, Speaker, Consultant, Advisor: Bristol Myers Squibb, Genentech/Roche, Grünenthal, Lilly, Merck Serono, MSD, Novartis, Pfizer. All other authors have declared no conflicts of interest.
Resources from the same session
868P - A DNA methylation classifier to predict recurrence from clear surgical margins
Presenter: tsima Abou Kors
Session: Poster session 12
869P - Utilizing H&E images and digital pathology to predict response to buparlisib in SCCHN
Presenter: Denis Soulieres
Session: Poster session 12
870P - Dynamic cfHPV DNA changes during induction chemotherapy as an early indicator of treatment responsiveness for locally advanced head and neck cancer patients
Presenter: Yilin Cao
Session: Poster session 12
871P - Detection of circulating tumor DNA in operable loco-regionally advanced HPV-negative head and neck squamous cell carcinoma
Presenter: Ludivine Beaussire
Session: Poster session 12
872P - Prognostic value of pathological intratumor heterogeneity in patients with head and neck squamous cell carcinoma treated with upfront surgery
Presenter: Constance Lamy
Session: Poster session 12
873P - Identification of PIK3CA mutation as a novel predictor of efficacious immunotherapy in head and neck cancer
Presenter: Zongwen Sun
Session: Poster session 12
875P - Proteomic and phosphoproteomic profiling of HNSCC and the role of CDKs as potential drug targets
Presenter: Konrad Klinghammer
Session: Poster session 12
876P - Gene expression analysis in oral potentially malignant disorders (OPMD) with dysplasia identifies patients at high risk of malignant transformation
Presenter: Loris De Cecco
Session: Poster session 12
877P - ROS1 mutations as potential negative predictor for response of immunotherapy in patient with head and neck cancer
Presenter: Yong Yuan
Session: Poster session 12