Abstract 408P
Background
Despite the recent progress of immune therapies and multi-kinase inhibitors such as Sora, the 5-year survival rate for late-stage HCC remains dismal. The high prevalence and distinct etiology of HCC in Asia Pacific represent high unmet medical needs. Considering EGFR and MET are frequently over-expressed in HCC and often correlate with poor prognosis, we evaluated the impact of Sora on EGFR and MET expression (expr) and TME in treating late-stage HCC. We also evaluated the association of EGFR and MET expr, etiology and TME.
Methods
Total 51 HCC patients (pts) with tumor tissues before 1st-line Sora treatment (Tx) and 43 paired post- Sora samples obtained for immunohistochemistry (IHC) and RNA sequencing (RNAseq) analysis. The formalin-fixed, paraffin-embedded (FFPE) tissues were analyzed for EGFR and MET expr by IHC using EGFR D38B1 and MET SP44 antibodies. Staining intensity was scored on a scale of 0, 1+, 2+ and 3+. RNAseq was successfully conducted in 60 FFPE tissues (33 pre- and 27 post- Sora samples) by TruSeq RNA Access library preparation. R package immunedeconv was used for TME estimation.
Results
The median duration of Sora Tx was 126 days for study group. Overall, H score of EGFR and MET expr was higher in post- Sora than in pre- Sora samples (Median value: EGFR 100 vs 55; MET 110 vs 85). On a pt level, increased EGFR and MET expr in IHC>=2+ was observed respectively in 53% and 41% of HCC pts post Sora Tx. Interestingly, H score of MET expr in HBV+ group was higher than that in HBV- group (p = 0.003). MET gene expr also showed similar trend (p = 0.002) but not for EGFR. Different cut-off for EGFR and MET IHC expr showed similar results as above. Furthermore, a trend of positive correlation was observed between robust MET IHC staining and myeloid dendritic cell activated score (RNAseq) post Sora Tx (n = 26).
Conclusions
This is the first time to report EGFR and MET IHC expr from pre- and post- Sora HCC samples using different cut off scores. EGFR and MET expr was higher in post- Sora than in pre- Sora samples. MET expr in HBV+ group was higher than that in HBV- group. The mechanisms and clinical significance of these observations warrant further investigation.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Janssen Research & Development.
Funding
Janssen Research & Development.
Disclosure
C.J. Yen: Non-Financial Interests, Institutional, Principal Investigator: National Cheng Kung University college of medicine- National Cheng Kung University Hospital. M. Qing, X. Lyu, M. Gormley, M. Xia: Financial Interests, Personal, Full or part-time Employment: Janssen Research & Development . J. Curtin, F. Yang, L. Zhou: Financial Interests, Institutional, Full or part-time Employment: Janssen Research & Development.
Resources from the same session
280P - Radium-223 for patients with metastatic castration-resistant prostate cancer with symptomatic bone metastases progressing after first-line abiraterone or enzalutamide: One institutional experience
Presenter: Keng Man Chiang
Session: Poster Display
Resources:
Abstract
281P - 10-year treatment outcome of prostate cancer patients with 3D conformal radiation: Experience of a single cancer institution in Iran
Presenter: Reyhane Bayani
Session: Poster Display
Resources:
Abstract
282P - Predictors of outcomes in patients with clinically lymph node-positive prostate cancer after definitive radiotherapy
Presenter: Jae-Sung Kim
Session: Poster Display
Resources:
Abstract
283P - Radiotherapy utilization rate and treatment patern of protate cancer at Cipto Mangunkusumo Central General Hospital (RSCM): What we learn from pre-pandemic era
Presenter: Riyan Apriantoni
Session: Poster Display
Resources:
Abstract
284TiP - CYCLONE 3: A phase III, randomized, double-blind, placebo-controlled study of abemaciclib in combination with abiraterone plus prednisone in men with high-risk metastatic hormone-sensitive prostate cancer
Presenter: Nobuaki Matsubara
Session: Poster Display
Resources:
Abstract
292P - Comparative characteristics of early cervical cancer diagnosis methods for Tashkent women
Presenter: Gulnoza Goyibova
Session: Poster Display
Resources:
Abstract
293P - Carboplatin in locally advanced cervical cancer treated with chemoradiation: An alternative to cisplatin
Presenter: Natalia Isabel Valdiviezo Lama
Session: Poster Display
Resources:
Abstract
294P - Concurrent chemoradiation with cisplatin every 3 weeks in locally advanced cervical cancer: A single arm phase II clinical trial
Presenter: Long Nguyen
Session: Poster Display
Resources:
Abstract
295P - A prospective study of dose escalated simultaneous integrated boost in node-positive cervical cancer
Presenter: Ritusha Mishra
Session: Poster Display
Resources:
Abstract
296P - Safety, efficacy, and immunogenicity of therapeutic vaccines for patients with high-grade cervical intraepithelial neoplasia (CIN 2/3) associated with human papillomavirus: A systematic review
Presenter: Caroline Amélia Gonçalves
Session: Poster Display
Resources:
Abstract