Efficacy of anti-VEGF & anti-EGFRs in microsatellite instable (MSI-H) metastatic colorectal cancer, Turkish Oncology Group (TOG) study.

e15507 Background: Mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) CRC tumors constitute of 5% of mCRC. Immunotherapy is a new standard, but it is difficult to give it all. 5FU based treatment with antiEGFRs in RAS/BRAF-wt or bevacizumab (B) is used in mCRC. Data is limited for the efficacy of B or antiEGFRs in dMMR/MSI-H mCRC due to small number of cases in CRC population in trials. Aims : Evaluation of prognostic factors &amp; 1 st line 5FU based treatment with B/antiEGFRs efficacy in mCRC. Methods: dMMR/MSI-H mCRC patients (pts) with 1 st line B/antiEGFRs were evaluated retrospectively. Results: 132 patients were included. Mutation rates were as 35.6% (n:47) for RAS, 12.1% (n:16) for BRAF.Median PFS was 10.9 (95%CI: 9.2-12.6) months. Median OS was 44 months (95% CI 26.23-63.03). 82 (62.1%) pts had primary tumor resection (PTR), 26 (19.7%) had PTR &amp; metastasectomy. 17 (12.8%) de novo mCRC pts had maximal cytoreductive surgery (MCS). 14 (10.6%) pts had subsequent IO. In multivariate analysis, RAS/BRAF mutation status, MCS &amp; subsequent IO are defined as prognostic factors for OS (p&lt;0.01, p: 0.022, p: 0.005, respectively). No statistically significant survival (PFS, OS) difference was detected. Conclusions: dMMR/MSI-H mCRC is an entity with different tumor biology. We consider that dMMR/MSI-H mCRC pts with BRAF wt, MCS &amp; subsequent IO have better outcomes with 1st line 5FU based treatment with B/antiEGFRs. Baseline characteristics &amp; survival analysis. n(%) PFS(months) OS (months) Univariate analysis Univariate analysis Multivariate analysis %95 CI P value %95 CI P value %95 CI HR P value Age (year) 60(23-82) 0.86 0.62 &lt;60 50 8.4-11.3 25.0-64.7 ≥60 72 9.8-15.1 17.4-71.8 Sex 0.55 Female 56(43.2) 7.5-14.7 6.7-58.5 0.59 Male 67(50.8) 7.5-12.4 26.9-62.3 Primary Tumor Location 0.045 0.036 Right 81(61.4) 7.9-10.7 24.7-85.6 Left 33(25) 9.1-15.8 16.0-73.7 <jats:t

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e15507
Citations
1
Primary Topic
Colorectal Cancer Treatments and Studies
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article
Field-Weighted Citation Impact
1.05
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article

Efficacy of anti-VEGF & anti-EGFRs in microsatellite instable (MSI-H) metastatic colorectal cancer, Turkish Oncology Group (TOG) study.

Murat Kiracı, Beliz Bahar Karaoğlan, Esma Türkmen, Nargız Majidova et al.
1 citations
Journal of Clinical Oncology
Colorectal Cancer Treatments and Studies
1.05
article

Efficacy of anti-VEGF & anti-EGFRs in microsatellite instable (MSI-H) metastatic colorectal cancer, Turkish Oncology Group (TOG) study.

Murat Kiracı, Beliz Bahar Karaoğlan, Esma Türkmen, Nargız Majidova, Sabin Göktaş Aydın, Taha Koray Şahin, Ali Oğul, Yakup Ergün, Zeynep Yüksel Yaşar, Emine Türkmen, Öztürk Ateş, Mutlu Doğan, Kadriye Başkurt, Elif Şahin, Abdullah Sakin, Ahmet Melih Arslan, Şafak Yıldırım Dişli, Mehmet Akif Öztürk, İlknur Deliktaş Onur, Eda Karapeli̇t Agi̇toğlu
article en
1 citations

Abstract

e15507 Background: Mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) CRC tumors constitute of 5% of mCRC. Immunotherapy is a new standard, but it is difficult to give it all. 5FU based treatment with antiEGFRs in RAS/BRAF-wt or bevacizumab (B) is used in mCRC. Data is limited for the efficacy of B or antiEGFRs in dMMR/MSI-H mCRC due to small number of cases in CRC population in trials. Aims : Evaluation of prognostic factors &amp; 1 st line 5FU based treatment with B/antiEGFRs efficacy in mCRC. Methods: dMMR/MSI-H mCRC patients (pts) with 1 st line B/antiEGFRs were evaluated retrospectively. Results: 132 patients were included. Mutation rates were as 35.6% (n:47) for RAS, 12.1% (n:16) for BRAF.Median PFS was 10.9 (95%CI: 9.2-12.6) months. Median OS was 44 months (95% CI 26.23-63.03). 82 (62.1%) pts had primary tumor resection (PTR), 26 (19.7%) had PTR &amp; metastasectomy. 17 (12.8%) de novo mCRC pts had maximal cytoreductive surgery (MCS). 14 (10.6%) pts had subsequent IO. In multivariate analysis, RAS/BRAF mutation status, MCS &amp; subsequent IO are defined as prognostic factors for OS (p&lt;0.01, p: 0.022, p: 0.005, respectively). No statistically significant survival (PFS, OS) difference was detected. Conclusions: dMMR/MSI-H mCRC is an entity with different tumor biology. We consider that dMMR/MSI-H mCRC pts with BRAF wt, MCS &amp; subsequent IO have better outcomes with 1st line 5FU based treatment with B/antiEGFRs. Baseline characteristics &amp; survival analysis. n(%) PFS(months) OS (months) Univariate analysis Univariate analysis Multivariate analysis %95 CI P value %95 CI P value %95 CI HR P value Age (year) 60(23-82) 0.86 0.62 &lt;60 50 8.4-11.3 25.0-64.7 ≥60 72 9.8-15.1 17.4-71.8 Sex 0.55 Female 56(43.2) 7.5-14.7 6.7-58.5 0.59 Male 67(50.8) 7.5-12.4 26.9-62.3 Primary Tumor Location 0.045 0.036 Right 81(61.4) 7.9-10.7 24.7-85.6 Left 33(25) 9.1-15.8 16.0-73.7 <jats:t

Journal of Clinical OncologyVol. 43(16_suppl)
Ankara University (TR), Manisa Celal Bayar University (TR), Bilkent University (TR), Dokuz Eylül University (TR), Istanbul Medipol University (TR), Memorial Ankara Hospital (TR), Necmettin Erbakan University (TR), Ankara Onkoloji Eğitim ve Araştırma Hastanesi (TR), Memorial Sisli Hospital (TR), Kayseri Eğitim ve Araştırma Hastanesi (TR), Sağlık Bilimleri Üniversitesi (TR), İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi (TR), Kocaeli Üniversitesi (TR), Hacettepe University (TR), Marmara University (TR)
Good health and well-being
Openalex Percentile: Top 21%
Colorectal Cancer Treatments and Studies
1.05
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