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
43P - Machine learning radiomics based on CT to predict response to lenvatinib plus tislelizumab based therapy for unresectable hepatocellular carcinoma
Presenter: Gang Chen
Session: Poster Display session
44P - Machine learning-based prediction of survival in patients with metastatic renal cell carcinoma receiving first-line immunotherapy
Presenter: Ahmed Elgebaly
Session: Poster Display session
45P - Gut microbiome signatures for exploring the correlation between gut microbiome and immune therapy response using machine learning approach
Presenter: Han Li
Session: Poster Display session
Resources:
Abstract
46P - Abnormal gut microbiota may cause PD-1 inhibitor-related cardiotoxicity via suppressing regulatory T cells
Presenter: Zeeshan Afzal
Session: Poster Display session
47P - Correlation of clinical, genetic and transcriptomic traits with PD-L1 positivity in TNBC patients
Presenter: Anita Semertzidou
Session: Poster Display session
48P - The A2AR antagonist inupadenant promotes humoral responses in preclinical models
Presenter: Paola Tieppo
Session: Poster Display session
49P - Highly potent novel armoured IL13Ra2 CAR T cell targeting glioblastoma
Presenter: Maurizio Mangolini
Session: Poster Display session
50P - Phase I trial of P-MUC1C-ALLO1 allogeneic CAR-T cells in advanced epithelial malignancies
Presenter: David Oh
Session: Poster Display session
51P - Unlocking CAR-T cell potential: Lipid metabolites in overcoming exhaustion in ovarian cancer
Presenter: Xiangyu Chang
Session: Poster Display session
Resources:
Abstract
52P - Tumor-targeted cytokine release by genetically-engineered myeloid cells rescues CAR-T activity and engages endogenous T cells against high-grade glioma in mouse models
Presenter: Federico Rossari
Session: Poster Display session