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
309P - Expression of estrogen receptor is a negative predictive biomarker for immunotherapy with lenvatinib plus pembrolizumab for advanced endometrial cancer with pMMR
Presenter: Hiroyuki Fujii
Session: Poster Display
Resources:
Abstract
310P - A study on the prediction of recurrence site of endometrial cancer using various machine learning techniques
Presenter: Wonkyo Shin
Session: Poster Display
Resources:
Abstract
311P - Circulating cytokines in the differential diagnosis of endometrial cancer
Presenter: Tatyana Abakumova
Session: Poster Display
Resources:
Abstract
312P - Molecular and genetic features of squamous cell carcinoma of vulvar cancer depending on HPV status
Presenter: Visola Navruzova
Session: Poster Display
Resources:
Abstract
313P - Efficacy and safety of oral metronomic chemotherapy in recurrent refractory advanced gynaecological cancer: Experience from regional cancer center of eastern India
Presenter: Ranti Ghosh
Session: Poster Display
Resources:
Abstract
314P - Perioperative outcomes in advanced epithelial ovarian cancer treated with neoadjuvant bevacizumab and chemotherapy: Real-world experience from an Indian cancer centre
Presenter: Upasana Palo
Session: Poster Display
Resources:
Abstract
315P - Real-world experience of niraparib as maintenance therapy in newly diagnosed advanced ovarian cancer: A single-center retrospective study
Presenter: Wenxin Liu
Session: Poster Display
Resources:
Abstract
316P - First evidence of olaparib maintenance therapy in patients with newly diagnosed BRCA wild-type ovarian cancer: A real-world multicenter study
Presenter: Jing Li
Session: Poster Display
Resources:
Abstract
317P - Attitudes of Israeli gynecologists towards risk reduction salpingo-oophorectomy at hysterectomy for benign conditions and the use of hormonal therapy
Presenter: wisam Assaf
Session: Poster Display
Resources:
Abstract
319P - Survival prediction for ovarian cancer patients from Taiwan cancer registry data
Presenter: Tzu-Pin Lu
Session: Poster Display
Resources:
Abstract