Abstract 390P
Background
Camrelizumab, a fully humanized monoclonal antibody against PD-1,has been approved in the treatment of advanced esophageal squamous carcinoma in China.The purpose of this study was to observe the efficacy and safety of Camrelizumab in the treatment of esophageal cancer in the real world.
Methods
This is an open-label,prospective,multicenter, observational study. Eligible patients (pts) who received camrelizumab had esophageal cancer; age≥18, ECOG PS of 0-2; and measurable disease.
Results
From August 1, 2019 to May 1, 2020. 100 pts were enrolled. There are 80 (80.0%) males. The median age was 65.0 yrs. The majority pts were at stage IV 74(74.0%), had prior surgery 47(47.0%) and radiotherapy 61(61.0%). Pts with ECOG PS 1-2 were 85 (85.0%). Metastases were detected in 88 (88.0%) pts, which mainly were lymphatic metastasis.Pts received first-line treatment, second-line, third-line or above, respectively were 20.0%, 31.0%, 48.0%. Before immunotherapy, only one patient was tested for PD-L1. Pts received apatinib monotherapy or in combination with chemotherapy or antiangiogenictherapy,respectively were 9.0%, 39.0%, 36.0%. There were 49 patients eligible for efficacy evaluation .9 achieved partial response, 30 had stable disease and 10 got progressive disease. Thus, the objective response rate (ORR) and disease control rate (DCR) were 18.4% and 79.6%. The incidence of AEs was 55 (55.0%) and the grade 3/4 treatment-related AEs was 3 (3.0) %. Main AEs were RCCEP (18.0%), and fatigue (17.0%), anorexia (11.0%). The grade 3/4 treatment-related AEs were RCCEP (1.0%), hypothyroidism (1.0%) and anemia(1.0%).
Conclusions
In real clinical applications, Camrelizumab is mostly used in patients with poor physical condition, metastatic and late stage, and most patients had front-line treatment.PD-L-1 detection is rarely performed in patients before medication, and most patients are treated with combination therapy of Camrelizumab.Camrelizumab is confirmed to be effective and safe in patients with esophageal cancer.Further analysis is needed to determine which factors are the positive factors in the treatment of Camrelizumab.
Clinical trial identification
Editorial acknowledgement
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
94P - Prognostic influence of mean platelet volume on stage III rectal cancer patients: A tertiary cancer center study
Presenter: Pavan Jonnada
Session: e-Poster Display Session
95P - Prognosis of Japanese patients with detailed RAS/BRAF mutant colorectal cancer
Presenter: Tatsuki Ikoma
Session: e-Poster Display Session
96P - Early-onset colorectal cancer prognosis, conflict resolution, review of literature and meta-analysis
Presenter: Ereny Poles
Session: e-Poster Display Session
97P - A population-based study to assess the associations of rural residence and low socioeconomic status (SES) with cardiovascular disease (CVD) in patients with colorectal cancer (CRC)
Presenter: Atul Batra
Session: e-Poster Display Session
98P - Operational challenges of an Asian Pacific (APAC) academic oncology clinical trial
Presenter: Daphne Day
Session: e-Poster Display Session
99P - Development of a qRT-PCR-based diagnostic test to identify colorectal cancer patients with recurrent R-Spondin gene fusions
Presenter: Veronica Diermayr
Session: e-Poster Display Session
100P - Individualized treatment of advanced digestive system tumour guided by PDTX mouse model: A multicenter trial
Presenter: yuan cheng
Session: e-Poster Display Session
101P - HIF1-α depletion overcomes resistance to oxaliplatin in colorectal cancer via ERK signalling pathway
Presenter: Se Jun Park
Session: e-Poster Display Session
102P - Colorectal cancer organoids culture exploits new neoadjuvant therapy resistance mechanisms and therapeutic targets
Presenter: Yun Deng
Session: e-Poster Display Session
103P - Comprehensive genomic landscape in younger and older Chinese patients with colorectal cancer
Presenter: Huina Wang
Session: e-Poster Display Session