Açık Akademik Arşiv Sistemi

Morbidity and long-term results in patients with wild and mutant type Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations undergoing colorectal cancer surgery

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dc.contributor.authors Aziret, Mehmet; Subasi, Ozkan; Bilir, Cemil; Tozlu, Mukaddes; Altintoprak, Fatih; Karaman, Kerem; Ercan, Metin; Celebi, Fehmi
dc.date.accessioned 2022-12-20T13:24:44Z
dc.date.available 2022-12-20T13:24:44Z
dc.date.issued 2022
dc.identifier.issn 0003-469X
dc.identifier.uri https://hdl.handle.net/20.500.12619/98943
dc.description Bu yayının lisans anlaşması koşulları tam metin açık erişimine izin vermemektedir.
dc.description.abstract BACKGROUND: In colorectal cancer (CRC), the mutation of the K(N)RAS gene has a significant impact on the clinical course, and is associated with a negative prognosis. We aim to present the morbidity and long-term results in patients with wild/mut-K(N)RAS, undergoing CRC surgery. METHODS: A total of 116 patients who underwent surgery for colorectal cancers with wild/mut-K(N)RAS were included in this retrospective study. The patients were divided into two groups: wild-K(N)RAS patients (Group 1) and mutant- K(N)RAS patients (Group 2). Results were evaluated for clinical, operative, morbidity and long-term survival outcomes. MATERIALS AND METHODS: The highest surgical site infection (SSI) rate (OR=140.339)(4.303-4581.307)(P=0.005) was seen in patients given Bevacizumab during neoadjuvant treatment. Meanwhile, the SSI site infection rate was at its lowest in cases where minimally invasive surgery was preferred (OR=0.062)(0.006-0.628)(P=0.019). In addition, the overall median survival rate for the total cohort was 38 +/- 3.1 (31-44) months. Multivariate analysis showed that CEA (>5ng/mL)(HR 2.94)(1.337-6.492))(P=0.007); tumor stage (P=0.034), T(T4) stage (HR 1.91)(1.605-252.6)(P=0.02); metastasectomy/ablation (HR 0.19)(0.077-0.520)(P=0.001); the number of removed metastatic lymph nodes (HR 1.08)(1.010-1.155)(P=0.025); tumor implant or nodule (HR 2.71)(1.102-6.706)(P=0.03); curative resection (HR 2.40)(0.878-6.580)(P=0.042) to be factors affecting the overall survival rate. CONCLUSION: Treatment with Bevacizumab during the neoadjuvant period in mut-K(N)RAS cases, surgical technique and complications of Grade 3 or higher are risk factors for SSI on morbidity in patients with mut/wild-K(N)RAS undergoing colorectal cancer surgery. Moreover, CEA (>5ng/mL), tumor stage, T stage, metastasectomy/ablation, the number of removed metastatic lymph nodes, tumor implant/nodule and curative resection are risk factors on the overall survival rate.
dc.language English
dc.language.iso eng
dc.subject Surgery
dc.subject Bevacizumab
dc.subject Colorectal cancer
dc.subject K(N)RAS mutation
dc.subject Morbidity
dc.subject Mortality
dc.title Morbidity and long-term results in patients with wild and mutant type Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations undergoing colorectal cancer surgery
dc.identifier.volume 93
dc.identifier.startpage 65
dc.identifier.endpage 77
dc.relation.journal ANNALI ITALIANI DI CHIRURGIA
dc.identifier.issue 1
dc.identifier.eissn 2239-253X
dc.contributor.author Aziret, Mehmet
dc.contributor.author Subasi, Ozkan
dc.contributor.author Bilir, Cemil
dc.contributor.author Tozlu, Mukaddes
dc.contributor.author Altintoprak, Fatih
dc.contributor.author Karaman, Kerem
dc.contributor.author Ercan, Metin
dc.contributor.author Celebi, Fehmi
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı


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