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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

5113 - Molecular profiles as a function of treatment response/progression free survival in a prospective cervical cancer study (RAIDs)

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Pathology/Molecular Biology

Tumour Site

Cervical Cancer

Presenters

Suzy Scholl

Citation

Annals of Oncology (2018) 29 (suppl_8): viii332-viii358. 10.1093/annonc/mdy285

Authors

S. Scholl1, L. De Koning2, M. Popovic3, D.L.R. Anne4, A. Floquet5, E. Berns6, G. Kenter7, A. Kereszt8, E. Girard9, H. von der Leyen10, S. Dureau11, V. Fourchotte12, R. Rouzier12, M. Kamal1, R. Consortium1

Author affiliations

  • 1 Department Of Drug Development And Innovation, Institut Curie, 75005 - Paris/FR
  • 2 Tranlationnal Department, Institut Curie, 75010 - Paris/FR
  • 3 Surgery, Institut of Oncology of Vojvodina, Novisad/RS
  • 4 Radiotherapy, Institut Curie, 75 - Paris/FR
  • 5 Oncologie Médicale, Institute Bergonié, 33076 - Bordeaux/FR
  • 6 Biology, ERASMUS, Rotterdam/NL
  • 7 Gynaecology, NKI, Amsterdam/NL
  • 8 Seqomics, SeqOmics, moraholem/HU
  • 9 Bioinformatics, Institut Curie, 75010 - Paris/FR
  • 10 Hctc, HCTC, hanover/DE
  • 11 Biometry, Institut Curie, 75010 - Paris/FR
  • 12 Surgery, Institut Curie, 75248 cedex5 - Paris/FR
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Abstract 5113

Background

BioRAIDs is a supervised longitudinal collection of tumor and blood together with clinical outcome data in 419 primary cervical cancer patients from 7 European countries (NCT02428842).

Methods

Molecular analysis [Next Generation Sequencing (NGS) at SeqOmics (Hungary) & Reverse Phase Protein array (RPPA) at Institut Curie] was performed on quality-controlled primary tumor samples in 295 patients (70%) who subsequently had received primary radio chemotherapy (RCT). Integrative bioinformatics analyses were performed to identify pathway activations suggesting the need for additional/different therapies.

Results

NGS demonstrated driver Tyrosine Kinase Receptor/ PI3 kinase (TKR/PI3K) pathway mutations in 27%; TKR/PI3K + epigenetic pathway alterations (MLL2, MLL3) in 32 % and epigenetic alterations alone in 13% of patients. At a median follow up of 19 months [2-38], tumors for which no mutations in relevant genes from the TKR/PI3K pathways nor alterations in genes involved in epigenetic signaling appeared to be associated with a significantly better prognostic profile: HR = 2.4 [95% CI: 1.1 – 5.2]. RPPA analysis was carried out separating patients in 3 subgroups according to signaling pathway activation [EMT (epithelial mesenchymal transition), DNA damage and MAPK/PI3K], none of which was associated with bad prognosis.

Conclusions

The high frequency of epigenetic alterations with or without TKR/PI3K pathway mutations, suggests that epigenetically acting drugs (VorinostatR) may be relevant for patients whose tumors have genetic mutations of significance in epigenetically acting enzymes. Relevance of copy number alterations and of other frequently mutated genes (CSMD3, SYNE1), needs to be integrated and cross validated in a larger complementary dataset.

Clinical trial identification

NCT02428842.

Legal entity responsible for the study

Institut Curie.

Funding

This project has received founding from the European Union’s Seventh Program for research, technological development and demonstration under grant agreement No 304810.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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