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Poster Display session

250P - Evaluating the impact of liquid biopsy-derived circulating tumor DNA (ctDNA) as predictive biomarkers in early-stage pancreatic cancer therapy response

Date

07 Dec 2024

Session

Poster Display session

Presenters

Hashim Talib Hashim

Citation

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

Authors

H.T. Hashim1, A.Q.M. Alhatemi2, O. Saab3

Author affiliations

  • 1 Department Of Research, University of Warith Al-Anbiyaa, College of Medicine, 10047 - Karbala/IQ
  • 2 Alnasiriya, Al Nasiriyah Teaching Hospital, 64001 - Dhi Qar/IQ
  • 3 Department Of Git, Hospital Medicine Department Cleveland Clinic, 44195 - Cleveland/US

Resources

This content is available to ESMO members and event participants.

Abstract 250P

Background

The evaluation of liquid biopsy-derived circulating tumor DNA (ctDNA) as predictive biomarkers in early-stage pancreatic cancer therapy response is critical for advancing personalized treatment strategies. The analysis of ctDNA offers a non-invasive method for monitoring tumor dynamics and therapeutic response, potentially guiding clinical decisions and enhancing outcomes in this challenging disease.

Methods

A systematic review and meta-analysis were conducted using data from the Cochrane Central Register of Controlled Trials (CENTRAL), PubMed, MEDLINE (including MEDLINE InProcess) (OvidSP), Web of Science, Embase (OvidSP), and Scopus databases. Risk of bias in randomized controlled trials (RCTs) was assessed using the ROB2 Cochrane tool. Statistical analysis was performed using RevMan Cochrane software.

Results

Data from 10 studies, encompassing a total of 1,234 patients, were combined, resulting in an odds ratio (OR) of 1.18 [95% CI: 0.58–2.41] for clinical success, indicating no significant difference (p = 0.64) between ctDNA and alternative methods, with moderate heterogeneity (I2 = 26%). Analyzing seven studies, which included 847 patients, for technical success yielded an OR of 1.64 [95% CI: 0.64–4.22] (p = 0.64), with 44% heterogeneity. Mortality data from three studies, covering 542 patients, indicated an OR of 0.99 [95% CI: 0.56–1.75] (p = 0.30), with 14% heterogeneity. No statistically significant differences were found for clinical success, technical success, or mortality between ctDNA and other procedures.

Conclusions

The meta-analysis revealed no significant differences in clinical success, technical success, or mortality between ctDNA and other methods in the pooled studies. These findings suggest comparable efficacy and outcomes, underscoring the necessity for further research to validate and optimize diagnostic approaches in clinical practice.

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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