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Poster Display session

470P - Nonlinear risks model in prediction of metachronous peritonel dissemination in radical treatment of gastric cancer

Date

27 Jun 2024

Session

Poster Display session

Presenters

Andrei Ivanov

Citation

Annals of Oncology (2024) 35 (suppl_1): S162-S204. 10.1016/annonc/annonc1482

Authors

A. Ivanov1, M. Reutovich2, O. Krasko3

Author affiliations

  • 1 State Institution N. N. Alexandrov National Cancer Centre of Belarus, Lesnoy - Minsk District/BY
  • 2 BSMU - Belarusian State Medical University, Minsk/BY
  • 3 The United Institute of Informatics Problems of the NAN of Belarus, Minsk/BY

Resources

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Abstract 470P

Background

After radical treatment of locally advanced gastric cancer (LAGC), there is a high risk of metachronous peritoneal dissemination (MPD), even after using various variants of intraperitoneal chemotherapy (IPC) and modern imaging techniques. The difficulty of early diagnosis of metachronous peritoneal dissemination (MPD) determines the necessity to estimate the probability of its development.

Methods

The analysis included long-term results of treating 1,311 patients with LAGC (pT1-4bN0-3M0, R.Borrmann scale III-IV) who underwent adjuvant therapy, normothermic intraperitoneal chemotherapy (NICT), hyperthermic intraperitoneal chemotherapy (HIPEC), adjuvant polychemotherapy (APCT) and their combinations. MPD risks were assessed using the Fine-Gray model.

Results

The intensity of MPD development was found to change over the 5-year follow-up period. To examine time-varying risk factors for MPD development, we used the Fine-Gray competing risks model with stratification by follow-up time intervals (1, 2, 3-5 years). The influence of age, pT, pN, degree of differentiation, tumor growth form, volume of surgical and adjuvant treatment was assessed. Risk ratios (95% Confidence Interval) were determined from the model and found to be:1) decreasing risk at the age >65 years with each year of follow-up - year 2 OR=0.53 (0.32-0.87), year 3-5 OR=0.59 (0.37-0.92); 2) MPD risks increased in patients with pN+, high grade adenocarcinoma and infiltrative LAGC; 3) risk reduction after APCT during the 1st year - OR=0.21 (0.08-0.52); 4) risk reduction during the 1st-5th year after IHT: NIHT OR=0.20 (0.09-0.45); IITHT OR=0.30 (0.18-0.50). The multidirectional influence of risk factors on MPD leads to the necessity estimating the period of maximum risk for MPD development based on individual patient factors. So the prognostic model was created and has a high prognostic value (C-index is 0.798, the AUC=0.835).

Conclusions

The non-linearity of risks should be taken into account when predicting MPD. Individualization of observation and risk assessment according to the proposed model will allow to make valid decisions on the timely application of ICT, which will increase the effectiveness of LAGC treatment.

Legal entity responsible for the study

Reutovich Michail.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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