Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

ePoster Display

1407P - Patterns of aggravation in gastric cancer patients with peritoneal metastases who underwent paclitaxel-based intraperitoneal therapy

Date

16 Sep 2021

Session

ePoster Display

Topics

Cytotoxic Therapy

Tumour Site

Gastric Cancer

Presenters

Yasushi Tsuji

Citation

Annals of Oncology (2021) 32 (suppl_5): S1040-S1075. 10.1016/annonc/annonc708

Authors

Y. Tsuji, T. Takayama, K. Sawai, S. Shindo, R. Moku, K. Iijima, R. Honma

Author affiliations

  • Medical Oncology Department, Tonan Hospital, 060-0004 - Sapporo/JP

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1407P

Background

We have shown promising results of intraperitoneal (ip) paclitaxel (PTX) in combination with systemic chemotherapy for gastric cancer (GC) with peritoneal metastases (PM) at the ESMO annual meeting in 2020 (Abstract 1535P). Of 157 patients (pts), median survival time (MST) was 13.5, and 36.8 mos. for 32 conversion surgery cases. ipPTX could provide significantly longer survival for GC pts with PM than conventional chemotherapy, and there were even several patients with the potential to be cured eventually. We analyzed patterns of aggravation and death in pts who underwent ipPTX to achieve better understanding of the disease and its potential outcomes.

Methods

We excluded cases with metastases other than peritoneal. There were GC 107 pts with PM only that received ipPTX from Feb 2013 to Dec 2020. 64 pts had the primary lesion and 43 pts underwent gastrectomy before ipPTX; their MST was 21.9 and 15.3 mos., respectively.

Results

83 (78%) out of 107 pts had aggravation. The most frequent site was the peritoneum, 52 pts. 68 pts (64%) died. 38 pts of these deaths were related to PM. 7 pts died of meningitis carcinomatosa. 32 pts out of 64 achieved conversion surgery, their MST was 36.8 mos. Out of the 32 pts, 21 (66%) recurred, which 16 pts related to PM and 1 to meningitis carsinomatosa. 16 pts (50%) died.

Conclusions

ipPTX in combination with systemic chemotherapy provided significantly longer survival than conventional chemotherapy for GC with PM. However, the majority of patients, including the conversion surgery cases, recurred and eventually died due to reaggravated peritoneal metastases. There were mainly two patterns of aggravation, one was resistance to ipPTX which caused multiple intestinal stenosis or obstruction, the other was limited distribution of ipPTX which in time allows for development of extra peritoneal metastases, causing mostly meningitis and rectal stenosis.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.