The Prognostic Value of Serum Semaphorin3A and VEGF Levels in Patients with Metastatic Colorectal Cancer.


Journal

Journal of gastrointestinal cancer
ISSN: 1941-6636
Titre abrégé: J Gastrointest Cancer
Pays: United States
ID NLM: 101479627

Informations de publication

Date de publication:
Jun 2020
Historique:
pubmed: 21 6 2019
medline: 4 2 2021
entrez: 21 6 2019
Statut: ppublish

Résumé

Despite new treatment options in metastatic colorectal cancer (mCRC), new prognostic markers are still needed to determine optimal chemoregimen especially for anti-angiogenesis drugs. In this study, we evaluated the serum semaphorin and VEGF-A levels as prognostic factors in patients with mCRC. Patients with diagnosed mCRC who were treated with first-line bevacizumab plus chemotherapy were included in the study. Venous blood samples of 37 patients with metastatic colon cancer were taken, and serum semaphorin 3A and VEGF-A levels were studied in pre-treatment and the 1st and third months after the treatment was initiated. Totally, 37 patients were enrolled in the study. The patients' mean age was 62 years. Twenty-eight (49%) of the patients were male, and 19 (51%) were female. Serum semaphorin3A (sema3A) levels of the patients were 5.4 ± 7.4 ng/ml before the treatment, 3.5 ± 3.3 ng/ml at the first month, and 3.5 ± 3.7 ng/ml at the third month. Serum VEGF-A levels were 27.7 ± 32.9 ng/l before the treatment, 23.1 ± 28.1 ng/l at the first month, and 28.9 ± 30.2 ng/l at the third month. There was no significant correlation between the survival and pre-treatment VEGF-A level (p = 0.064). Overall survival (OS) was statistically significantly higher in patients with pre-treatment semaphorin 3A levels below 5.4 ng/ml than higher than 5.4 ng/ml (10.5 months vs 4.5 months, respectively, HR 0.23, 95% CI 19.635-11,391, p = 0.012). Pre-treatment semaphorin 3A level can be a prognostic marker for the mCRC patients who were treated with bevacizumab in patients with metastatic colorectal cancer.

Identifiants

pubmed: 31218581
doi: 10.1007/s12029-019-00263-4
pii: 10.1007/s12029-019-00263-4
doi:

Substances chimiques

Biomarkers, Tumor 0
SEMA3A protein, human 0
Semaphorin-3A 0
VEGFA protein, human 0
Vascular Endothelial Growth Factor A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

491-497

Subventions

Organisme : 151518014
ID : 1

Auteurs

Tuba Karpuz (T)

Department of Internal Medicine, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

Murat Araz (M)

Department of Internal Medicine and Medical Oncology, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey. zaratarum@yahoo.com.

Levent Korkmaz (L)

Department of Internal Medicine and Medical Oncology, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

Ibrahim Kılınc (I)

Department of Biochemistry, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

Sidika Findik (S)

Department of Pathology, Saraykoy Akyokus Street, Necmettin Erbakan University Meram Faculty of Medicine, postal code, 42080, Konya, Turkey.

Mustafa Karaagaç (M)

Department of Internal Medicine and Medical Oncology, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

Melek Karakurt Eryilmaz (MK)

Department of Internal Medicine and Medical Oncology, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

Mehmet Artac (M)

Department of Internal Medicine and Medical Oncology, Necmettin Erbakan University Meram Faculty of Medicine, Saraykoy Akyokus Street, 42080, Konya, Turkey.

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Classifications MeSH