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Poster Display session

141P - Predictive MINT pathological risk score for adjuvant chemotherapy in resected cholangiocarcinoma: A propensity score matched multicenter study in Thailand

Date

07 Dec 2024

Session

Poster Display session

Presenters

Kaewta Jeerapradit

Citation

Annals of Oncology (2024) 35 (suppl_4): S1450-S1504. 10.1016/annonc/annonc1688

Authors

K. Jeerapradit1, C. Sookthon2, K. Sriudomporn1, S. Chansitthichok3, W. Ouransatien3, W. Suragul4, S. Boonpob5, P. Sarkhampee3, N. Ngamphaiboon1, J. Juengsamarn6

Author affiliations

  • 1 Division Of Medical Oncology, Department Of Medicine, Mahidol University - Faculty of Medicine - Ramathibodi Hospital, 10400 - Bangkok/TH
  • 2 Department Of Medicine, Sisaket Hospital, 33000 - Sisaket/TH
  • 3 Department Of Surgery, Sunpasitthiprasong Hospital, 34000 - Ubon Ratchathani/TH
  • 4 Division Of Hepatobiliary And Pancreatic Surgery, Department Of Surgery, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH
  • 5 Department Of Surgery, Sisaket Hospital, 33000 - Sisaket/TH
  • 6 Department Of Medicine, Sunpasitthiprasong Hospital, 34000 - Ubonratchathani/TH

Resources

This content is available to ESMO members and event participants.

Abstract 141P

Background

Curative surgery is a mainstay treatment for resectable cholangiocarcinoma (CCA). The role of adjuvant chemotherapy (AC) in such patients remains controversial. This retrospective study aimed to identify patients who would benefit from AC.

Methods

Resected CCA patients undergoing curative surgery, with or without AC, were identified from 3 cancer centers in Thailand. R2 resection were excluded. Using the largest center as the discovery cohort, we generated propensity scores matching (PSM). Uni/multivariate Cox regression analyses for overall survival (OS) were conducted in the PSM discovery cohort to identify factors and develop a predictive risk score, which classified patients into high and low-risk groups. The proposed risk score was validated in the other 2 centers.

Results

In the discovery cohort, 493 patients were identified. After PSM, 328 patients were categorized into surgery (N=164) and surgery + AC (N=164) groups. The baseline characteristics in the PSM discovery cohort were well balanced. In the validation cohort, patients with a positive pathological lymph node received AC more frequently than those under observation (47% vs 18%; p=0.02). A MINT pathological risk score was developed from multivariate analysis for OS. In PSM discovery cohort, for low-risk score, the surgery group has significantly longer OS compared to the surgery + AC group (49.4 vs 31.5 months, HR 1.78 [1.11-2.86]; p 0.016). Conversely, for high-risk score, the surgery + AC group has better OS than the surgery group [18.8 vs 8.0 months, HR 0.60 (0.46-0.79); p < 0.001]. The results were comparable in the validation cohort. Table: 141P

MINT Risk Factor (Score) Cohort HR (95% CI) p-value
Surgical Margin (1) Discovery (n=328) 1.31 (1.02 - 1.70) 0.04
Perineural Invasion (1) 1.36 (1.03 - 1.79) 0.03
Lymph Node – pN1 (2) pNx (1) 1.87 (1.40 - 2.50) 1.42 (1.02 - 1.98) <0.01 <0.01
Tumor size (≥ 5 cm) (1) 1.39 (1.09 - 1.78) <0.01
Low risk (0-1) Validation (n=83) 3.11 (1.06 – 9.17) 0.04
High risk (≥ 2) 0.70 (0.35 – 1.39) 0.31

Conclusions

Resected CCA patients with high-risk MINT pathological risk score were likely to benefit from AC, while those with a low-risk score were not. Further validation in a larger prospective cohort is warranted.

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.

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