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Machine Learning-Guided Personalized Immunochemotherapy Strategies in Intrahepatic Cholangiocarcinoma
Jun-Hao Mei1, Kai Zhang2, Ying Zhang1
1Center of Interventional Radiology & Vascular Surgery, Nurturing Center of Jiangsu Province for State Laboratory of AI Imaging & Interventional Radiology (Southeast University), Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing, China; State Key Laboratory of Digital Medical Engineering, National Innovation Platform for Integration of Medical Engineering Education (NMEE) (Southeast University), Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
Background & Aims:
Immunochemotherapy (IO-chemo) has become standard care for patients with unresectable intrahepatic cholangiocarcinoma (iCCA), but benefit of adding IO varies greatly among individuals. We sought to develop a system to identify patients most likely to benefit from this treatment based on individualized treatment effect (ITE) estimation.
Methods:
This study included patients with unresectable iCCA who underwent either IO-chemo or chemotherapy alone (chemo). Patients were enrolled from three discovery and seven external validation centers. Target trial emulation was employed to obtain unbiased average treatment effect estimation, and a causal machine-learning model was used to estimate heterogeneous treatment effects for IO-chemo. Based on predicted ITE, patients were stratified into high-benefit, no- to moderate-benefit, and negative-benefit groups, with overall survival used as the primary end point.
Results:
The discovery cohort included 1485 patients; the external validation cohort included 562 patients. In the high-benefit group, compared with chemo, the hazard ratio (HR) for IO-chemo was 0.39 (95% CI, 0.30-0.52; p < 0.001), with mortality reduced by 24.1%, 31.2%, and 28.5% at 12, 24, and 36 months, respectively. In the no- to moderate-benefit group, IO-chemo did not differ from chemo (HR, 0.91; 95% CI, 0.70-1.18; p = 0.488). In the group with negative predicted ITEs, IO-chemo was associated with shorter OS than chemo (HR, 1.91; 95% CI, 1.47-2.48; p < 0.001). In the external validation cohort, the corresponding HRs were 0.45 (95% CI, 0.30-0.68; p < 0.001), 0.62 (95% CI, 0.42-0.93; p = 0.018), and 1.93 (95% CI, 1.28-2.91; p = 0.002), respectively.
Conclusions:
A causal machine learning-based model can estimate individualized treatment effects of immunochemotherapy in patients with unresectable intrahepatic cholangiocarcinoma, enabling clinically meaningful benefit stratification.
Impact And Implications:
The overarching goal of intrahepatic cholangiocarcinoma (iCCA) management is to deploy biomarkers that identify patients most likely to benefit from immunochemotherapy and thus enable personalized therapy, but little research has examined how clinicians choose between chemotherapy and immunochemotherapy beyond head-to-head efficacy comparisons or efforts to define subgroups suited to a single regimen. Built on a causal machine-learning (ML) framework, the Causal ML-Guided Personalized Immunochemotherapy Strategies in Intrahepatic Cholangiocarcinoma model described here offers a validated, clinically practical tool to quantify the benefit of immunochemotherapy in iCCA. In this study, 17 clinical variables were used to reliably identify patients most likely to benefit from immunochemotherapy and to predict long-term survival. By focusing on individualized treatment effects rather than average treatment effects, the model provides a strong foundation for future trials that seek to operationalize intelligent treatment selection and pushes precision immunochemotherapy for iCCA closer to routine practice.
Clinical Trial Number:
NCT06849193.
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