Abstract 149P
Background
Thymic carcinoma(TC) is the most aggressive subtype of thymic epithelial tumors. According to previous clinical trials, immunotherapy was proved to be effective in second line of treatment. Hence a phase II, prospective clinical trial was conducted by our research team to explore the safety and efficacy of toripalimab (a PD-1 inhibitor) combined with chemotherapy as first line treatment in advanced TC.
Methods
We enrolled patients with histologically diagnosis of Masaoka stage III or IV TC. Patients received toripalimab (240mg, d1, q3w) plus paclitaxel (175mg/m2, d1, q3w) and carboplatin (AUC=5, d1, q3w) for 4-6 cycles and continued to receive toripalimab (240mg, d1, q4w) maintenance therapy until disease progression, intolerable toxicity, or withdrawal of consent. The primary endpoint was progression-free survival (PFS). Secondary endpoints were objective response rate (ORR), Disease control rate (DCR), duration of response (DoR), overall survival (OS), time to response (TTR) and safety.
Results
From December 27th, 2020 to June 6th, 2024, 24 patients were enrolled. Median age was 55 years (range: 35–69) and 16 (66.7%) patients were male. 11(45.8%) patients were still on toripalimab maintenance treatment at the time of analysis. For 24 patients received radiological evaluation, best overall response of 8 partial response, 16 stable disease were observed. Accordingly, the ORR was 33.3% and DCR was 100.0%. Median PFS was 25.3 months (95% CI: 14.1-36.5), 1-year PFS rate was 72.0%, 2-year PFS rate was 63.0%. The median follow-up duration was 16.18 months (range: 1.57-41.8). Treatment-related adverse event (TRAE) of any-grade occurred in 23 patients. Grade 3-4 TRAE occurred in 10 patients. The most common grade 3-4 TRAE was neutrophil count decrease. Furthermore, we observed that the patients with lower TMB had more CD8+T cells and CD56dim NK subtype. Patients with PD-L1 TPS≥1% had a higher proportion of M1 type macrophages, suggesting a greater potential for activating antitumor immunity.
Conclusions
Toripalimab combined with chemotherapy is effective and well tolerated as first line treatment for patients with advanced thymic carcinoma.
Clinical trial identification
ChiCTR2000039155.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
226P - Profiling of gastric adenocarcinomas from EU and LATAM countries identifies distinct tumor immune subgroups and a central role of the tumor microbiome in shaping the immune microenvironment
Presenter: Manuel Cabeza Segura
Session: Poster Display session
228P - Modulating mitochondrial dynamics in TAMs to enhance anti-tumor immunity
Presenter: Pu-ste Liu
Session: Poster Display session
Resources:
Abstract
229P - Investigation of the effects of long-noncoding RNA NRAV on interferon response in melanoma
Presenter: Kadir Durmus
Session: Poster Display session
230P - Deciphering the mechanism of immunosuppressive activity of acetaminophen in the context of cancer immunotherapy
Presenter: Jeanne Lena
Session: Poster Display session
231P - The impact of calcitriol and tacalcitol on the Th17 lymphocytes in breast cancer
Presenter: Beata Filip-Psurska
Session: Poster Display session