Advanced gallbladder cancer with high tumor mutation burden: a case report and literature review

被引:0
作者
Wang, Juan [1 ,2 ,3 ]
Liu, Jianmin [2 ,3 ,4 ]
Yan, Chao [5 ]
Wang, Kai [5 ]
Li, Qiuyao [6 ]
Yu, Jie [2 ,3 ,5 ]
机构
[1] Southwest Med Univ, Affiliated Hosp, Dept Oncol, Luzhou, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Dept Radiat Oncol, Jinan, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Prov Key Lab Radiat Oncol, Jinan, Peoples R China
[4] Weifang Med Univ, Sch Clin Med, Affiliated Hosp, Weifang, Peoples R China
[5] Shandong Univ, Qilu Hosp Qingdao, Cheeloo Coll Med, Dept Radiotherapy, 758 Hefei Rd, Qingdao 266035, Peoples R China
[6] Shandong Univ, Qilu Hosp Qingdao, Cheeloo Coll Med, Dept Pathol, Qingdao, Peoples R China
来源
AME CASE REPORTS | 2024年 / 8卷
关键词
Advanced gallbladder cancer (advanced GBC); biliary tract cancer (BTC); immunotherapy; tumor mutation burden (TMB); case report; BILIARY-TRACT CANCER; GEMCITABINE PLUS CISPLATIN; FOLFIRINOX; S-1;
D O I
10.21037/acr-23-188
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Gallbladder cancer (GBC) is a common malignant tumor of the biliary system. It is characterised by insidious onset, rapid progression and poor prognosis. Symptoms often indicate advanced or late-stage disease, with a 5-year survival rate of only 5-15%. Case Description: We present a case study of a patient with GBC who had a tumor mutation burden (TMB) of 32.5/MB (>= 10 muts/MB). The patient received mFOLFIRINOX as first-line chemotherapy, which demonstrated significant efficacy. After stabilizing the disease, a sequential chemotherapy regimen was chosen. This regimen combined the immune checkpoint inhibitor (ICI) toripalimab (JS001), a humanised IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1), with S-1 therapy, an oral fluoropyrimidine derivative. However, this treatment did not provide any significant clinical benefit for the patient. Therefore, we hypothesise that combining immunotherapy with chemotherapy may be more effective as a first line treatment for high-TMB advanced GBC. This hypothesis needs to be validated in large-scale clinical studies. Conclusions: In summary, mFOLFIRINOX is a safe and effective first-line chemotherapy regimen for advanced GBC. The timing of combining immunotherapy with chemotherapy requires careful consideration. Further clinical trials involving immunotherapy in advanced GBC are necessary to identify biomarkers that can guide clinical decisions.
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页数:10
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