New Prognostic Factors in Colorectal Cancer
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Keywords

colon cancer
adjuvant chemotherapy
chemokine receptors
prognostic factors

How to Cite

Orlova, R. V., Ivanova, A. K., Raskin, G. A., & Kutukova, S. I. (2024). New Prognostic Factors in Colorectal Cancer. Voprosy Onkologii, 70(5), 928–935. https://doi.org/10.37469/0507-3758-2024-70-5-928-935

Abstract

Introduction. Colorectal cancer represents a significant proportion of the total number of cancer cases. Cancer screening has led to more cases being diagnosed at an early stage, allowing more patients to receive adjuvant chemotherapy. At present, there are known prognostic factors that influence the inclusion of adjuvant chemotherapy in the treatment plan. However, these factors do not include the biological and molecular genetic characteristics of the tumor. The search for new prognostic factors may lead to a shift in treating colorectal cancer patients.

Aim. To identify the most effective adjuvant chemotherapy regimen by evaluating the impact of a range of prognostic and additional factors (Ki67 index proliferation, KRAS mutation, chemokine receptor expression) on progression-free survival in colon cancer patients following radical surgical treatment.

Materials and Methods. The study included 113 patients diagnosed with stage II (Group A) or stage III (Group B) colon cancer following surgical treatment. All patients were treated in accordance with the standards available at the time. Patients in Group A received only surgical treatment, while patients in Group B received complex treatment (surgical treatment + adjuvant chemotherapy). The entire patient cohort was observed for 60 months, and then divided into subgroups depending on whether distant metastases had been detected. The next stage was to analyze clinical characteristics of the patients, including age, gender, localization of the primary tumor and type of surgery performed. The morphological characteristics of the tumor were also examined, including the expression level of Ki-67, the presence and level of expression of chemokine receptor CCRX4 and molecular genetic analysis (determination of mutations in codons 12,13 of the KRAS gene).

Results. Further prognostic factors influencing progression-free survival rates were identified, including expression of the CXCR4 chemokine receptor, the Ki-67 proliferation index and tumor localization.

Conclusion. The additional prognostic factors identified in this study can be used to optimize complex treatments for colon cancer patients.

https://doi.org/10.37469/0507-3758-2024-70-5-928-935
##article.numberofdownloads## 36
##article.numberofviews## 130
pdf (Русский)

References

Каприн А.Д. Состояние онкологической помощи населению России в 2022 году. Москва. 2023; 239.- ISBN 978-5-85502-283-4. [Kaprin A.D. The state of oncological care for the population of Russia in 2022. 2023; 239.-ISBN 978-5-85502-283-4 (In Rus)].

Практические рекомендации по лечению злокачественных опухолей Российского общества клинической онкологии, версия 2023. RUSSCO. 2023; 451-453.-URL: https://rosoncoweb.ru/standarts/RUSSCO/. [Practical recommendations for the treatment of malignant tumors of the Russian Society of Clinical Oncology, version 2023. RUSSCO. 2023; 451-453.-URL: https://rosoncoweb.ru/standarts/RUSSCO/ (In Rus)].

Gerdes J., Schwab U., Lemke H., et al. Producing of a mouse monoclonal antibody reactive with a human nuclear antigen associated with cell proliferation. Int J Cancer. 1983; 31(1): 13-20.-DOI: https://doi.org/10.1002/ijc.2910310104.

Conlin A., Smith G., Carey F.A., et al. The prognostic significance of K-ras, p53, and APC mutations in colorectal carcinoma. Gut. 2005; 54(9): 1283-6. DOI: https://doi.org/10.1136/gut.2005.066514.

Tie J., Lipton L., Desai J., et al. KRAS mutation is associated with lung metastasis in patients with curatively resected colorectal cancer. Clin Cancer Res. 2011; 17(5): 1122-30.-DOI: https://doi.org/10.1158/1078-0432.

Schlechter B.L., Stebbing J. CCR5 and CCL5 in metastatic colorectal cancer. J ImmunoTher Cancer. 2024; 12: e008722.-DOI: https://doi.org/10.1136/jitc-2023-008722.

Hanahan D., Weinberg R. The hall marks of cancer: the next generation. Cell. 2011; 144(5): 646-74.-DOI: https://doi.org/10.1016/j.cell.2011.02.013.

Susek K.H., Karvouni M., Alici E., et al. The role of CXC chemokine receptors 1–4 on immune cells in the tumor microenvironment. Front Immunol. 2018; 9: 2159.-DOI: https://doi.org/10.3389/fimmu.2018.02159.

Kato M., Kitayama J., Kazama S., et.al. Expression pattern of CXC chemokine receptor-4 is correlated with lymph node metastasis in human invasive ductal carcinoma. Breast Cancer Res. 2003; 5: R144-R150.-DOI: https://doi.org/10.1186/bcr627.

Rivera C.G., Bader J.S., Popel A.S. Angiogenesis-associated crosstalk between collagens, CXC chemokines, and thrombospondin domain-containing proteins. Ann Biomed Eng. 2011; 39(8): 2213-22.-DOI: https://doi.org/10.1007/s10439-011-0325-2.

Shi Y., Riese D.J., Shen J. The role of the CXCL12/CXCR4/CXCR7 chemokine axis in cancer. Front Pharmacol. 2020; 11.-DOI: https://doi.org/10.3389/fphar.2020.574667.

Bedeer A.E., El-Ghaffar Heabah N.A. Evaluation of C-X-C chemokine receptor type 4 (CXCR4) and Peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in colorectal carcinoma: Relation to the available clinicopathological parameters. Indian J Pathol Microbiol. 2023; 66(3): 465-471.-DOI: https://doi.org/10.4103/ijpm.ijpm_481_21.

Li J., Huang L., Zhao H., et al. The role of interleukins in colorectal cancer. Int J Biol Sci. 2020; 16(13): 2323-2339.-DOI: https://doi.org/10.7150/ijbs.46651.

Ottaiano A., Scala S., Normanno N., et al. Prognostic and predictive role of CXC chemokine receptor 4 in metastatic colorectal cancer patients. Appl Immunohistochem Mol Morphol. 2020; 28(10): 755-60.-DOI: https://doi.org/10.1097/pai.0000000000000828.

Iveson T., Sobrero A.F., Yoshino T., et al. Prospective pooled analysis of four randomized trials investigating duration of adjuvant (adj) oxaliplatin-based therapy (3 vs 6 months {m}) for patients (pts) with high-risk stage II colorectal cancer (CC). J Clin Oncol. 2019; 37(15_suppl): 3501-3501. DOI: https://doi.org/10.1200/jco.2019.37.15_suppl.3501.

Herrera M., Mezheyeuski A., Villabona L., et al. Prognostic interactions between FAP+ fibroblasts and CD8a+ T cells in colon cancer. Cancers. 2020; 12(11): 3238.-DOI: https://doi.org/10.3390/cancers12113238.

Azcue P., Guerrero Setas D., Encío I., et al. A novel prognostic biomarker panel for early-stage colon carcinoma. Cancers. 2021; 13(23): 5909.-DOI: https://doi.org/10.3390/cancers13235909.

Dienstmann R., Salazar R., Tabernero J. Personalizing colon cancer adjuvant therapy: selecting optimal treatments for individual patients. J Clin Oncol. 2015; 33(16): 1787-96.-DOI: https://doi.org/10.1200/jco.2014.60.0213.

Kim J., Mori T., Chen S.L., et al. Chemokine receptor CXCR4 expression in patients with melanoma and colorectal cancer liver metastases and the association with disease outcome. Ann Surg. 2006; 244(1): 113-20.-DOI: https://doi.org/10.1097/01.sla.0000217690.65909.9c.

Pircher A., Hilbe W., Heidegger I., et ak. Biomarkers in tumor angiogenesis and anti-angiogenic therapy. Int J Mol Sci. 2011; 12(10): 7077-99.-DOI: https://doi.org/10.3390/ijms12107077.

Grimm F., Maurus R., Beschorner R., et al. Ki-67 labeling index and expression of p53 are non-predictive for invasiveness and tumor size in functional and nonfunctional pituitary adenomas. Acta Neurochir. 2019; 161(6): 1149-56.-DOI: https://doi.org/10.1007/s00701-019-03879-4.

Stintzing S., Tejpar S., Gibbs P., et al. Understanding the role of primary tumour localisation in colorectal cancer treatment and outcomes. Eur J Cancer. 2017; 84: 69-80.-DOI: https://doi.org/10.1016/j.ejca.2017.07.016.

Tie J., Lipton L., Desai J., et al. KRAS mutation is associated with lung metastasis in patients with curatively resected colorectal cancer. Clin Cancer Res. 2011; 17(5): 1122-30.-DOI: https://doi.org/10.1158/1078-0432.ccr-10-1720.

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