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Poster Display

124P - Characteristics, prognosis and therapeutic effects of non-V600 BRAF mutated colorectal cancer

Date

02 Dec 2023

Session

Poster Display

Presenters

Lalida Arsa

Citation

Annals of Oncology (2023) 34 (suppl_4): S1502-S1519. 10.1016/annonc/annonc1378

Authors

L. Arsa1, N. Ngamphaiboon2, A. Jinawath3, N. Sripaiboonkij4, N. Jinawath5, E. Sirachainan6, T. Siripoon7

Author affiliations

  • 1 Pathology, Mahidol University - Faculty of Medicine - Ramathibodi Hospital, 10400 - Bangkok/TH
  • 2 Medicine, Mahidol University - Faculty of Medicine - Ramathibodi Hospital, 10400 - Bangkok/TH
  • 3 Pathology, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH
  • 4 Ramathibodi Comprehensive Cancer Center, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH
  • 5 6. integrative Computational Bioscience Center, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH
  • 6 Medicine Department, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH
  • 7 Medical Oncology Department, Mahidol University - Faculty of Medicine Ramathibodi Hospital, 10400 - Bangkok/TH

Resources

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Abstract 124P

Background

BRAF V600E is identified approximately 5-9% of colorectal cancer (CRC) patients. Non-V600E BRAF mutation is characterized a rare molecular subtype. The clinical characteristics and prognostic impact of non-V600 BRAF mutants are not well defined.

Methods

We recruited 829 patients with CRC from our institution. Tissue samples were molecularly tested. Clinical data was retrospectively reviewed and analyzed using Chi-square and t-test. Overall survival (OS) was compared by log-rank test.

Results

All BRAF mutation was detected in 50 (6%) patients including 24 (3%) patients with non-V600 mutations. Patient characteristics and BRAF testing technique were not significantly different based on BRAF status and it was comparable between BRAF V600E and non-V600 groups. There were significantly more ALL RAS and PIK3CA mutations in non-V600 mutant patients. Patients with non-V600 mutation had median OS of 82 months which was longer than BRAF WT, 66 months, and 31 months of BRAF V600E group, respectively (P=0.067). OS according to treatment with anti-EGFR in metastatic CRC patients was not significantly different in both V600E and non-V600 BRAF mutant groups. Table: 124P

BRAF-MT (n=50)
BRAF-WT (n=779) BRAF-MT (n=50) p-value V600 (n=26) non-V600 (n=24) p-value
Age 63 (18 - 93) 65 (19-85) 66 (19 - 85) 65 (24 - 83)
Sex
Male 471 (60) 32 (64) 0.62 15 (58) 17 (71) 0.333
Female 308 (40) 18 (36) 11 (42) 7 (29)
Sidedness
Left 591 (76) 33 (66) 0.289 12 (70) 15 (62) 0.878
Right 168 (22) 15 (30) 7 (27) 8 (33)
non-specify 20 (3) 2 (4) 1 (4) 1 (4)
Technique
NGS 547 (70) 38 (76) 0.466 18 (69) 20 (83) 0.26
Pyrosequencing 84 (11) 6 (12) 5 (19) 1 (4)
PCR 148 (19) 6 (12) 3 (12) 2 (12)
All RAS mutation 418 (54) 8 (16) <0.001 0 8 (33) 0.001
PIK3CA mutation 94 (12) 9 (18) 0.218 1 (4) 8 (33) 0.009
Recur/Met (n=575) (n=35) (n=19) (n=16)
Anti-VEGF 105 (18) 7 (20) 0.796 2 (11) 5 (31) 0.207
Anti-EGFR 162 (28) 6 (17) 0.156 3 (16) 3 (19) 1

Conclusions

Non-V600 BRAF mutation may indicate better prognosis. The difference in treatment effect was not demonstrated in patients with BRAF mutation.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Faculty of medicine Ramathibodi Hospital.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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