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Poster Display session

139P - Young onset colorectal cancer: Clinical and molecular characteristics

Date

27 Jun 2024

Session

Poster Display session

Presenters

Christos Cortas

Citation

Annals of Oncology (2024) 35 (suppl_1): S1-S74. 10.1016/annonc/annonc1477

Authors

C. Cortas1, G.M. Saridakis2, I. Messaritakis3, M. Karagianni4, M. Chondrozoumaki5, G. Tsironis1, C. Matthaiou6, I. Souglakos7, D. Papamichael1

Author affiliations

  • 1 Bank of Cyprus Oncology Centre, Nicosia/CY
  • 2 UOC - University of Crete, Heraklion/GR
  • 3 German Oncology Center, Yiannoukas Medical Labs,Bioiatriki Group, Limasol/CY
  • 4 University of Crete - School of Medicine, Heraklion/GR
  • 5 University of Crete - School of Medcine, Heraklion/GR
  • 6 Bank of Cyprus Oncology Centre, 2006 - Nicosia/CY
  • 7 University General Hospital of Heraklion, Heraklion/GR

Resources

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Abstract 139P

Background

The incidence of Young Onset Colorectal Cancer (YO-CRC) has been increasing globally over the last few years.

Methods

Retrospective study based on data extraction from medical records at two Cancer centers, in Crete and Cyprus from 1999 to 2023. Patients were managed according to standard of care treatment and contemporary guidelines. Clinical and molecular data were collected and correlated with DFS, PFS and OS using SPSS software.

Results

A total of 334 patients were identified; 53% were female and the median age at diagnosis was 44 years (range 18-50); 68% colon and 32% rectal cancers. The median time between onset of symptoms and diagnosis was 3 months. Commonest presenting symptoms were bleeding per rectum (37,4%), weight loss (36,2%), change in bowel habit (27,5%) and bloating (19,5%). The median BMI of patients was 25. YO-CRC represented just under 6% of all colorectal cases. Molecular testing was done in patients with available tissue either prospectively or retrospectively. Table: 139P

AJCC Stage 3-year DFS 5-year OS
Stage I (8,6%) 100% 100%
Stage II (23,9%) 78,7% 91,2%
Stage III (38%) 65,6% 69%
Median PFS 5-year OS
Stage IV (29,5%) 7 months 20,5%
Mutations and MSI status according to the site of the tumor
Right colon (26,9%) Left colon (72,5%) Overall
MSH 27,7% 9% 16% (20/125)
ALL RAS 44,4% 50% 48,4% (59/122)
BRAF 13,4% 6,1% 8,3 (8/96)

Conclusions

Patients with YO-CRC present with similar pathogenic mutations as their older counterparts. More YO-CRC are diagnosed with metastatic disease at presentation than expected.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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