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

Poster Display session

297P - Real-life efficacy of immune checkpoint inhibitors in microsatellite unstable/mismatch repair-deficient (dMMR/MSI-H) biliary tract cancer (BTC)

Date

27 Jun 2024

Session

Poster Display session

Presenters

Alice BOILEVE

Citation

Annals of Oncology (2024) 35 (suppl_1): S119-S161. 10.1016/annonc/annonc1481

Authors

I. Campo le Brun1, E. Grapinet2, A. Hollebecque3, V. Aurillac2, P. Parent4, P. Girot5, M. Gendreau6, S. Rafert7, S. Javed8, Y. Touchefeu9, G. Roth10, M. MULLER11, M. Lequoy12, A. BOILEVE3, M. Decraecker2

Author affiliations

  • 1 UVSQ Paris-Saclay, Versailles/FR
  • 2 CHU de Bordeaux-Hôpital Haut-Lévêque, Pessac/FR
  • 3 Institut Gustave Roussy, Villejuif, Cedex/FR
  • 4 CHU Lille - Centre Hospitalier Régional Universitaire de Lille, Lille/FR
  • 5 CHD Vendée, La Roche-sur-Yon/FR
  • 6 Centre Hospitalier Universitaire Henri-Mondor AP-HP, Creteil/FR
  • 7 CHU Poitiers, Poitiers/FR
  • 8 Centre Hospitalier de Valenciennes, Valenciennes/FR
  • 9 CHU du Nantes - Hôtel-Dieu, Nantes, Cedex/FR
  • 10 CHU Grenoble-Alpes, La Tronche/FR
  • 11 CHRU Nancy, Nancy/FR
  • 12 Hopital Saint-Antoine, Paris/FR

Resources

Login to get immediate access to this content.

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

Abstract 297P

Background

Immune checkpoint inhibitors (ICIs) are known to improve oncological outcomes in patients (pts) with mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI) solid tumours. ICI have obtained approval in 2022 as first-line treatment in combination with chemotherapy for advanced biliary tract cancer (BTCs) but MSI/dMMR BTCs are a rare subtype whose response to ICI is poorly describe. This multicentre study aims to describe clinical characteristics and the therapeutic strategy in current practice in pts with MSI/dMMR BTC.

Methods

We retrospectively included and collected data from all consecutive pts with MSI/dMMR BTC treated in 11 French centers. We reported outcomes (overall survival (OS) and progression free survival (PFS), according to RECIST V1.1) and tolerance particularly regarding ICI administration.

Results

Overall, 34 pts with MSI/dMMR BTC were included between 2015 and 2022. At diagnosis, 32% had a locally advanced stage and 29% were metastatic. More than 50% of pts had liver metastases.Twenty-eight (82%) patients received ICIs, including 5 in 1st line combined with chemotherapy, 2 in 1st line as monotherapy and 21 in subsequent line as monotherapy. Pts receiving ICI had a median OS from the initial diagnosis of 28.2 mts (CI95: 16.9-54.4) vs 15.6 mts (CI95: 5.8-18.1) for those who did not receive any ICI ; 60.7% of pts were still alive 2 years after ICI and 42.8% after 3 years. When ICI was used in 1st line, OS was 28.2 mts (CI95: 15.8 - 54.4) and PFS was 22.4 mts (CI95: 15.0 - 61.3). When ICI was used in ≥ 2 line, OS was 28.8 mts (CI95:17.8 - 48.3) and PFS was 5 mts (CI95: 0.0 - 10.7). OS from the start of ICI whatever the line was 14.2 mts (CI95: 6.8 - 29.1) and PFS was 10.8 mts (CI95: 5.8 - 20.5). Two pts had grade 3-4 irAE and 8 developed all grades irAE. Two pts were rechallenged with ICI after progression.

Conclusions

This is the first large real-world cohort which reports efficacy and tolerance of ICIs in pts MSI/dMMR BTC.

Legal entity responsible for the study

AGEO.

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.