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
53P - Novel ex-vivo manufacturing of transiently expressed armoured CAR T cells for glioblastoma
Presenter: Saket Srivastava
Session: Poster Display session
54P - Superior antitumor activities of fourth-generation CAR-T cells containing three costimulatory domains targeting GD2-positive tumors
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
55P - Engineering of chimeric cytokine receptors (CCR) to induce IL-7 signaling to CAR-T cells for solid tumor treatment
Presenter: Marta Soria Castellano
Session: Poster Display session
56P - Potent antitumor efficiency of CD19-CAR T cells self-secreting PD-L1 x CD3 BiTE against aggressive B-cell lymphoma
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
57P - SENDER™ Directed LNP Delivery of mRNA for In Situ generation of highly potent CAR T Cells
Presenter: Biao Ma
Session: Poster Display session
58P - Cardiovascular outcomes of novel CAR-T cell therapies: A meta-analysis of incidence, risk factors, and management of cardiotoxicity
Presenter: Hashim Talib Hashim
Session: Poster Display session
59P - Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials
Presenter: Nicolas Mach
Session: Poster Display session
60P - Innovative applications of neoantigens in dendritic cell-derived exosome (DEX) therapy and their impact on personalized cancer treatment
Presenter: Ramon Gutierrez
Session: Poster Display session
61P - Optimized protocol for the accelerated production of dendritic cell-derived exosomes (DEXs): Achieving speed without compromising efficacy
Presenter: Ramon Gutierrez
Session: Poster Display session
62P - Ecto-CRT induction of NKp46 surface expression increases osimertinib-resistant lung cancer’s sensitivity to NK cells
Presenter: Sumei Chen
Session: Poster Display session