Abstract 971P
Background
Currently, the prognosis of advanced intrahepatic cholangiocarcinoma (ICC) is poor, and the current treatment methods are not effective. There is some clinical evidence that chemotherapy combined with programmed cell death protein-1(PD-1) inhibitors and tyrosine kinase inhibitor (TKI) can help improve the clinical outcomes of patients with advanced ICC.
Methods
We retrospectively screened patients with advanced intrahepatic cholangiocarcinoma (ICC) who received chemotherapy combined with lenvatinib and PD-1.We evaluated overall survival (OS), progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), tumor shrinkage rate, and safety.
Results
We enrolled 95 patients with ICC and divided them into three groups. The median follow-up duration was 15.1 months. The chemotherapy group (Chemo group), chemotherapy combined with immune checkpoint inhibitors (Dual-regimen group), and chemotherapy-ICI-lenvatinib (Triple-regimen group) had median OS of 13.1 months, 20.8 months, and 39.6 monthsrespectively.Notably, the triple-regimen group demonstrated a significantly longer OS than the chemotherapy and dual-regimen groups did. For PFS, the chemo group, dual-regimen group, and triple-regimen group reported median durations of 4.8 months, 11.9 months, and 23.4 months, respectively. Both combination groups showed significantly longer PFS than the chemotherapy -only group (P<0.05). The average early tumor shrinkage rates in the three groups were 1.676 %, -36.55%, and -34.22%.The combination therapy groups exhibited better tumor shrinkage than the chemotherapy group (P<0.05). The ORR in the were 18.2%, 55.5%, and 54.7%, respectively. The DCRs were 72.7%, 90%, and 96.2%, respectively, indicating significantly better outcomes in the combination therapy group. In addition, Two patients with ICC experienced significant tumor shrinkage after treatment and underwent surgical resection.
Conclusions
The combination of chemotherapy with PD-1 inhibitors and lenvatinib demonstrated considerable efficacy and tolerability as a treatment strategy for patients with advanced ICC.
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
498P - Report of 9 cases of embryonal tumours of the central nervous system with multilayered rosettes (ETMR)
Presenter: Ruyu Ai
Session: Poster session 17
Resources:
Abstract
499TiP - A phase II study of BPM31510 (a lipid nanodispersion of oxidized CoQ10) with vitamin K in combination with standard of care (SOC) RT and TMZ in glioblastoma multiforme (GBM) patients without prior therapy
Presenter: Brian Stockdale
Session: Poster session 17
500TiP - Update on GBM AGILE: A global, phase II/III adaptive platform trial to evaluate multiple regimens in newly diagnosed and recurrent glioblastoma
Presenter: Michael Weller
Session: Poster session 17
501TiP - Clinical performance evaluation of a brain cancer liquid biopsy
Presenter: James Cameron
Session: Poster session 17
692P - Role of adjunctive surgery after platinum-based chemotherapy in management patients with adrenocortical carcinoma: Observation study
Presenter: Yaroslav Zhulikov
Session: Poster session 17
693P - Causes of death in patients with malignant adrenal tumors: A population-based analysis
Presenter: Shangqing Ren
Session: Poster session 17
946P - Ipilimumab and nivolumab in advanced hepatocellular carcinoma after failure of prior atezolizumab and bevacizumab treatment: A multicenter retrospective study
Presenter: Jung Sun Kim
Session: Poster session 17
948P - Drug type and duration of adjuvant immune checkpoint inhibitors in hepatocellular carcinoma with high-risk recurrence factors (PREVENT): An update analysis of a prospective, multicentric cohort study
Presenter: Jia-Yong Su
Session: Poster session 17
Resources:
Abstract
949P - Update results of ALTER-H006: A phase II study of TQB2450 plus anlotinib as adjuvant therapy in hepatocellular carcinoma (HCC) with high risk of recurrence after surgical resection
Presenter: Xianhai Mao
Session: Poster session 17
950P - Outcomes by baseline tumour burden in EMERALD-1: A phase III, randomised, placebo (PBO)-controlled study of durvalumab (D) ± bevacizumab (B) with transarterial chemoembolisation (TACE) in participants (pts) with embolisation-eligible unresectable hepatocellular carcinoma (uHCC)
Presenter: Masatoshi Kudo
Session: Poster session 17