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

190P - EORTC-SPECTA Arcagen project: Results of the prospective rare thoracic tumors cohort

Date

31 Mar 2023

Session

Poster Display session

Presenters

Marco Tagliamento

Citation

Journal of Thoracic Oncology (2023) 18 (4S): S137-S148.
<article-id>elcc_Ch09

Authors

M. Tagliamento1, M. Morfouace2, C. Loizides2, J. Oliveira3, L. Greiller4, J. Raimbourg5, A.C. Toffart6, T. Chatelier7, N. Cloarec8, I. Sullivan9, B. Brasiuniene10, J. Peron11, K. Oselin12, M. Robert2, C. Fernandes2, A. Poncin2, J. Blay13, B. Besse14, N. Girard15

Author affiliations

  • 1 Villejuif/FR
  • 2 EORTC Headquarters, Bruxelles/BE
  • 3 Instituto Portugues de Oncologia do Porto Francisco Gentil, Porto/PT
  • 4 Hopital Nord (APHM), Marseille/FR
  • 5 Nantes Université, Institut de Cancerologie de l'Ouest, Saint-Herblain/FR
  • 6 Grenoble Alpes University, Grenoble Alpes Hospital, Grenoble/FR
  • 7 Clinique Mutualiste de l’Estuaire - Centre d'Oncologie, Saint Nazaire/FR
  • 8 Centre Hospitalier d'Avignon, Avignon/FR
  • 9 Hospital de la Santa Creu i Sant Pau, Barcelona/ES
  • 10 National Cancer Institute, Faculty of Medicine, Vilnius/LT
  • 11 CHU de Lyon - Hôpital Lyon Sud, Lyon/FR
  • 12 Clinic of Oncology and Hematology, North Estonia Medical Centre, Tallinn/EE
  • 13 Centre Léon Bérard, Lyon/FR
  • 14 Institut Gustave Roussy, Villejuif/FR
  • 15 Institut Curie, 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 190P

Background

Rare cancers are usually under-represented in clinical research including genomic profiling. Arcagen is a European study aiming at defining the molecular landscape of rare cancers for treatment guiding. We present data from the prospective cohort of rare thoracic tumors.

Methods

Patients with malignant pleural mesothelioma (MPM) or thymic tumors (TT) at advanced stage underwent genomic profiling by FoundationOne CDx on FFPE blocks, or alternatively by FoundationOne Liquid CDx on newly collected plasma samples. Molecular tumor boards (MTB) discussed patients’ molecular and clinical profile to advise for possible biomarker-guided treatments, including clinical trial options.

Results

Overall, 102 patients recruited from 8 different countries between July 2019–May 2022 were evaluable: 56 patients with MPM, 46 with TT (23 thymomas, 23 thymic carcinomas). One third were female (21% for MPM, 54% for TT), the median age at diagnosis was 70 (IQR 55–74), 29% of the patients were first managed with a curative intent (9% MPM, 54% TT). Molecular profiling was performed on 70 FFPE samples (42 MPM, 28 TT), while in 32 cases the analysis was done on cfDNA (14 MPM, 18 TT), within a median turnaround time of 8 days. We detected relevant molecular alterations in 64 out of 102 patients (63%; 77% MPM, 46% TT), specifically in 49 of 70 FFPE samples (70%; 88% MPM and 32% TT) and 15 of 32 plasma samples (47%; 43% MPM and 50% TT). The most frequently altered genes were CDKN2A/B, BAP1, MTAP in MPM, while TP53, CDKN2A/B, SETD2 in TT. The tumor mutational burden was low across all tumor types (mean 3.2 Muts/MB), 2 tumors had MSI-high status. MTB advised for potential treatment options in 39 situations (including non-biomarker driven trials in 8 cases), for 17 MPM and 22 TT patients, and gave indication to genetic or hematologic counseling for 7 patients (mostly due to the detection of germline pathogenic variants in BAP1 or clonal hematopoiesis).

Conclusions

We found relevant genomic alterations in 63% of rare thoracic tumors, allowing broadening the treatment options for at least 30% of the patients according to MTB recommendation. cfDNA analysis efficiently recovered cases that had inadequate tumor material. Molecular testing and drug accessibility should be implemented for these patients.

Clinical trial identification

NCT02834884.

Legal entity responsible for the study

European Organisation for Research and Treatment of Cancer (EORTC).

Funding

Roche.

Disclosure

M. Tagliamento: Other, Personal, Other, Travel, Accommodations, Expenses: Roche, Bristol Myers Squibb, AstraZeneca; Other, Personal, Writing Engagements: Novartis, Amgen, MSD. M. Morfouace: Other, Personal, Full or part-time Employment: Merck Healthcare KGAa. J. Oliveira: Financial Interests, Personal, Other, Advisory board, Invited speaker: AstraZeneca, Roche, Novartis, Janssen; Financial Interests, Personal, Invited Speaker: GSK, BMS, MSD, Bayer; Financial Interests, Personal, Advisory Board: Eisai; Financial Interests, Institutional, Funding, Investigator Initiated Clinical Trial funding: AstraZeneca. A.C. Toffart: Other, Institutional, Research Grant: Roche, Pfizer, BMS; Non-Financial Interests, Personal, Other: Roche, Pfizer, BMS, Novartis, Vifor Pharma, Amgen, Takeda, AstraZeneca; Other, Personal, Other: Novartis, Vifor Pharma, Amgen, Takeda, AstraZeneca, Boehringer Ingelheim, MSD. B. Brasiuniene: Other, Personal, Other, Travel, Accommodation, Speaker: AstraZeneca, Bristol Myers Squibb, Novartis, Roche, Eli Lilly, MSD, Janssen. K. Oselin: Other, Personal, Other, Travel, Accommodations, Expenses: MSD, AstraZeneca; Other, Personal, Other, Consultations Fees: Amgen, Takeda, Roche, AstraZeneca, Janssen, Johnson & Johnson. J. Blay: Financial Interests, Personal, Advisory Board: Bayer, Deciphera, GSK, Roche; Financial Interests, Personal, Invited Speaker: PharmaMar; Financial Interests, Institutional, Invited Speaker: MSD; Financial Interests, Personal, Other, member of the supervisory board: Innate Pharma; Financial Interests, Institutional, Funding: MSD, BMS, Deciphera; Financial Interests, Institutional, Research Grant: AstraZeneca, Roche, Bayer, GSK, Novartis, OSE pharma. B. Besse: Financial Interests, Institutional, Funding: 4D Pharma, AbbVie, Amgen, Aptitude Health, AstraZeneca, BeiGene, Blueprint Medicines, Boehringer Ingelheim, Celgene, Cergentis, Cristal Therapeutics, Daiichi-Sankyo, Eli Lilly, GSK, Janssen, Onxeo, OSE immunotherapeutics, Pfizer, Roche-Genentech, Sanofi, Takeda, Tolero Pharmaceuticals; Financial Interests, Institutional, Research Grant: Genzyme Corporation, Chugai Pharmaceutical, Eisai, Inivata, Ipsen, Turning Point Therapeutics. N. Girard: Financial Interests, Personal, Invited Speaker: AstraZeneca, BMS, MSD, Roche, Pfizer, Mirati, Amgen, Novartis, Sanofi; Financial Interests, Personal, Advisory Board: AstraZeneca, BMS, MSD, Roche, Pfizer, Janssen, Boehringer Ingelheim, Novartis, Sanofi, AbbVie, Amgen, Eli Lilly, Grunenthal, Takeda, Owkin; Financial Interests, Institutional, Research Grant, Local: Roche, Sivan, Janssen; Financial Interests, Institutional, Funding: BMS; Non-Financial Interests, Personal, Officer, International Thymic malignancy interest group, president: ITMIG; Other, Personal, Other, Family member is an employee: AstraZeneca. All other 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.