Results of a prospective single-center randomized study on the role of neoadjuvant chemotherapy in the combined treatment of patients with stage III colon cancer (Node-Rads scores 3-5)
https://doi.org/10.18027/2224-5057-2025-049
Abstract
Background: The optimal treatment strategy for patients with stage III colon cancer remains a subject of active research. While adjuvant chemotherapy (ACT) following surgery is the current standard, the potential role of neoadjuvant chemotherapy (NeoACT) in improving treatment outcomes is increasingly being investigated.
Objective: To evaluate the impact of neoadjuvant chemotherapy (NeoACT) on surgical outcomes in patients with stage III colon cancer (Node-RADS scores 3-5).
Materials and methods: A prospective, single-center, randomized clinical trial included 108 patients divided into two groups: NeoACT (n = 54) and primary surgery (n = 54). Patients in the NeoACT group received chemotherapy using either the CapOX regimen (4 cycles) or FOLFOX6 (6 cycles), followed by surgery. Surgical outcomes (operation duration, intraoperative blood loss, conversion rate, postoperative complications according to Clavien-Dindo, and length ofhospital stay) and pathological findings were analyzed.
Results: NeoACT did not adversely affect surgical outcomes. The median operation time was 180 minutes, and the median hospital stay was 8.7 days. Intraoperative blood loss was 50-100 ml in both groups. A statistically significant increase in conversion from laparoscopy to laparotomy was observed in the NeoACT group (p = 0.046). The rates of Clavien-Dindo grade 3a — b complications were 4.2 % and 3.8 %, respectively (p = 1). NeoACT resulted in a higher rate of pNO (p < 0.001), reduced incidence of pT4b (p = 0.053) and pN2 (p = 0.06), and lower presence of lymphovascular invasion (p < 0.001). Only 59.3 % of patients in the NeoACT group required 3 months of ACT, compared to 71.2 % of patients in the primary surgery group who received 6 months (p < 0.001).
Conclusion: NeoACT does not increase the rate of postoperative complications and contributes to tumor downstaging, leading to reduced need for adjuvant chemotherapy. The inclusion of patients with Node-RADS scores 4-5 minimized the risk of overtreatment from 25% to 8%.
About the Authors
M. A. DanilovaRussian Federation
Danilova Margarita Alekseevna
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
N. N. Semenov
Russian Federation
Semenov Nikolai Nikolaevich
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
M. A. Danilov
Russian Federation
Danilov Mikhail Aleksandrovich
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
A. V. Leontev
Russian Federation
Leontev Aleksandr Vladimirovich
Build. Novogireevskaya St., Moscow 111123
Build. 1 9/14 Meshchanskaya St., Moscow 129090
Competing Interests:
The authors declare that there are no possible conflicts of interest.
G. G. Saakyan
Russian Federation
Saakyan Georgii Germanovich
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
V. A. Aliev
Russian Federation
Aliev Vyacheslav Afandievich
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
P. S. Feoktistova
Russian Federation
Feoktistova Polina Sergeevna
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
V. V. Tsvirkun
Russian Federation
Tsvirkun Viktor Viktorovich
Build. Novogireevskaya St., Moscow 111123
Competing Interests:
The authors declare that there are no possible conflicts of interest.
References
1. Bregni G., Rebuzzi S.E., Sobrero A. The optimal duration of adjuvant therapy for stage iii colon cancer: the European perspective. Curr Treat Options in Oncol 2019;20 (1). https://doi.org/10.1007/sll864-019-0600-2
2. Morton D., Seymour M., Magill L., et al. preoperative chemotherapy for operable colon cancer: mature results of an international randomized controlled trial. J Clin Oncol 2023;41(8):1541-1552. https://doi.org/10.1200/JCO.22.00046
3. Hu H., Huang M., Li, Yu., et al. Perioperative chemotherapy with mFOLFOX6 or CAPOX for patients with locally advanced colon cancer (OPTICAL): A multicenter, randomized, phase 3 trial. J Clin Oncol 2022;40:16_suppl. https://doi.org/10.1200/JC0.2022.40.16_suppl.3500
4. Yang L., Ma W., Wang M., et al. Efficacy of intestinal obstruction stent combined with laparoscopic surgery and neoadjuvant chemotherapy in patients with obstructive colorectal cancer. Oncol Lett 2019;18(2):1931-1937. https://doi.org/10.3892/ol.2019.10525
5. Wei S., Xi J., Cao S., et al. Laparoscopic radical resection combined with neoadjuvant chemotherapy in treatment of colorectal cancer: clinical efficacy and postoperative complications. Am J Transl Res 2021;13(12):13974-13980
6. Davey M.G., Amir A.H., Ryan O.K., et al. Evaluating the oncological safety of neoadjuvant chemotherapy in locally advanced colon carcinoma: a systematic review and meta-analysis of randomised clinical trials and propensity-matched studies. IntJ Colorectal Dis 2023;38(l):193. https://doi.org/10.1007/s00384-023-04482-x
7. Karoui M., Rullier A., Piessen G., et al. Perioperative FOLFOX 4 versus FOLFOX 4 plus cetuximab versus immediate surgery for high-risk stage II and III colon cancers: a phase ii multicenter randomized controlled trial (PRODIGE 22). Ann Surg 2020;271(4):637-645. https://doi.org/10.1097/SLA.0000000000003454
8. Garcia del Alamo Hernandez Y., Cano-Valderrama O., Cerdan-Santacruz C., et al. Diagnostic accuracy of abdominal ct for locally advanced colon tumors: can we really entrust certain decisions to the reliability of CT? J Clin Med 2023;12(21):6764. https://doi.org/10.3390/jcml2216764
9. Nerad E., Lahaye M.J., Maas M., et al. Diagnostic accuracy of CT for local staging of colon cancer: a systematic review and meta-analysis. AmJ Roentgenol 2016;207(5):984-995. https://doi.org/10.2214/AJR.15.15785
10. Meyer H.J., Schnarkowski B., Pappisch J., et al. CT texture analysis and node-RADS CT score of mediastinal lymph nodes — diagnostic performance in lung cancer patients. Cancer Imaging 2022;22(l):75. https://doi.org/10.1186/s40644-022-00506-x
11. Leonardo C., Flammia R.S., Lucciola S., et al. Performance of Node- RADS scoring system for a standardized assessment of regional lymph nodes in bladder cancer patients. Cancers (Basel) 2023;15(3):580. https://doi.org/10.3390/cancersl5030580
12. Lucciola S., Pisciotti M.L., Frisenda M., et al. Predictive role of Node- RADS score in patients with prostate cancer candidates for radical prostatectomy with extended lymph node dissection: comparative analysis with validated nomograms. Prostate Cancer Prostatic Dis 2023;26(2):379—387. https://doi.org/10.1038/s41391-022-00564-z
13. Loch F.N., Beyer K., Kreis M.E., et al. Diagnostic performance of Node Reporting and Data System (Node-RADS) for regional lymph node staging of gastric cancer by CT. Eur Radiol 2024;34(5):3183—3193. https://doi.org/10.1007/s00330-023-10352-5
14. Gorshkova М.А., Semenov N.N., Danilov М.А., Vasnev O.S., Kulezneva Yu.V., Lesko K.A., Prosikov V.A. Application of the Node-RADS system for evaluation of regional lymph nodes based on computed tomography data in colon cancer patients. Malignant tumours. 2024;14(3):40-48 (In Russ.), https://doi.org/10.18027/2224-5057-2024-024
15. Lynch A., Arean-Sanz R., Ore A., et al. Impact of neoadjuvant chemotherapy for locally advanced colon cancer on postoperative complications. Langenbecks Arch Surg 2023;408(1):365. https://doi.org/10.1007/s00423-023-03094-x
16. Maggialetti N., Greco C.N., Lucarelli N.M., et al. Applications of new radiological scores: the Node-RADS in colon cancer staging [published correction appears in Radiol Med 2024;129(3):524. https://doi.org/10.1007/sll547-023-01755-x. Radiol Med 2023;128(11):1287-1295. https://doi.org/10.1007/sll547-023-01703-9
17. Zhong J., Mao S., Chen H., et al. Node-RADS: a systematic review and meta-analysis of diagnostic performance, category-wise malignancy rates, and inter-observer reliability. Eur Radiol 2025;35(5):2723-2735. https://doi.org/10.1007/s00330-024-11160-l
18. Sassun R., Sileo A., Ng J.C., et al. Oncological outcomes of neoadjuvant chemotherapy versus upfront surgery in locally advanced colon cancer: a systematic review, meta-analysis, and sequential analysis. Ann Surg Oncol 2025. https://doi.org/10.1245/sl0434-025-17640-y
19. Benson A.B., Venook A.P., Al-Hawary M., et al. Rectal Cancer, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Cane Netw 2022;20(10):1139-1167. https://doi.org/10.6004/jnccn.2022.0051
20. Argiles G., Tabernero J., Labianca R., et al. Localised colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2020;31(10):1291—1305. https://doi.Org/10.1016/j.annonc.2020.06.022
21. Clinical Guidelines. Malignant neoplasm of the colon, 2021. Available at: https://oncology-association.ru/clinical-guide-lines (In Russ.).
Review
For citations:
Danilova M.A., Semenov N.N., Danilov M.A., Leontev A.V., Saakyan G.G., Aliev V.A., Feoktistova P.S., Tsvirkun V.V. Results of a prospective single-center randomized study on the role of neoadjuvant chemotherapy in the combined treatment of patients with stage III colon cancer (Node-Rads scores 3-5). Malignant tumours. 2025;15(3):29-39. (In Russ.) https://doi.org/10.18027/2224-5057-2025-049
 
                    
 
        



























 
             
  Email this article
            Email this article