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Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

4171 - KRAS-dependent and independent mechanisms of progressive disease (PD) in colorectal cancer (CRC) patients (pts) with liver metastases (LM) while monitoring on circulating cell free DNA (cfDNA)

Date

21 Oct 2018

Session

Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

Topics

Targeted Therapy

Tumour Site

Colon and Rectal Cancer

Presenters

Andrey Kirov

Citation

Annals of Oncology (2018) 29 (suppl_8): viii150-viii204. 10.1093/annonc/mdy281

Authors

A. Kirov1, Z. Mihaylova2, V. Petrova2, T. Todorov3, D. Petkova2, A. Garev2, A. Todorova-Georgieva4

Author affiliations

  • 1 Human Genetics, Independent Medico-Diagnostic Laboratory Genome Centre Bulgaria, 1612 - Sofia/BG
  • 2 Department Of Medical Oncology, Military Medical Academy, 1606 - Sofia/BG
  • 3 Human Genetics, Genetic Medico-Diagnostic Laboratory Genica, 1612 - Sofia/BG
  • 4 Medical Chemistry And Biochemistry, Medical University Sofia, 1431 - Sofia/BG
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Resources

Abstract 4171

Background

KRAS mutational analysis (MA) in plasma (P) cfDNA is an alternative to tissue (T) analysis with concordance rate (ConR) from 30 to 90%. The emergence of KRAS mutation (M) during the course of anti-EGFR therapy is responsible for acquired resistance (AR). We aimed to evaluate the RAS ConR between T and cfDNA in mCRC pts, and to monitor changes in RAS M status.

Methods

All blood samples were collected in cfDNA Preservative Tubes (Norgen Biotek Corp., Canada). ctDNA was extracted within 3 days after sampling, the extraction was performed by commercial kit (P/Serum cfDNA Purification Mini Kit, Norgen Biotek). KRAS (ex 2) M on P cfDNA and tumor T were detected by real-time PCR kits TheraScreen: K-RAS Mutation Kit. The other M were detected by Sanger sequencing (BigDye Terminator v3.1 Cycle Sequencing Kit - Thermo Fisher Scientific).

Results

In the ConR evaluation were enrolled prospectively 63 mCRC pts. Only LM had 52,4% (33) pts, from whom - 27,3% (9) pts had primary resectable LM. The median time from T biopsy (primary -97%) to P collection was 275, 7 days (range 26 - 1560). TMA revealed 58,7% (37) M pts from whom 78,4% (29) pts had KRAS ex.2 M. cfDNA evaluation showed the distribution of M to wild (W) - 81%/19% with KRAS ConR of 58,7%. To reduce time between T and P samples MA in the monitoring analysis were included only 31 pts who had primary unresectable LM, with baseline (b) P collection. In 5 pts with KRAS M after converting treatment, LM resection resulted in W type on consecutive cfDNAs. In responding pts (10) with W disease on bcfDNA, there was no change in MA consequently. In non-responders with W type the appearance of KRAS M was noted in 6 pts, while in the rest 3 pts PD was not correlated to KRAS M. In non-responders with KRAS M on bcfDNA (6 pts), monitoring of cfDNA revealed disappearance of KRAS M contemporary with mainly LM PD.

Conclusions

The estimated ConR between primary tumor and cfDNA KRAS MA was 58%. The emergence of KRAS M in W type pts reveled AR to anti-EGFR therapy. In pts with M KRAS on bcfDNA, liver resection in responders and LM PD in non-responders correlated with loss of KRAS M as a mechanism of AR to anti-angiogenesis treatment in the later.

Clinical trial identification

Legal entity responsible for the study

Prof. Albena Parvanova Todorova-Georgieva.

Funding

Medical University Sofia.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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