Comparative analysis of treatment of patients with metastatic colorectal cancer using local destruction methods
https://doi.org/10.17238/2072-3180-2026-1-116-122
Abstract
Introduction. Approximately 90 % of liver tumors are metastatic, predominantly from colorectal cancer (CRC). Only 10–25 % of such metastases are resectable. The median survival is less than a year without treatment and even with chemotherapy it does not exceed 18 months. The aim of the study to improve the effectiveness of treatment for patients with colorectal cancer liver metastases using minimally invasive local destruction methods.
Materials and methods of research. The study included 257 patients with CRC liver metastases (2002–2024). All patients underwent ultrasound, contrast-enhanced MRI/CT, PET-CT, and 3D modeling (MYRIAN XP-Liver) for treatment planning. All patients received combined therapy: chemotherapy according to FOLFOX/XELOX/FOLFIRI regimens ± targeted therapy.
Transarterial chemoembolization (TACE): 34 patients (to shrink tumors >4 cm). Radiofrequency ablation (RFA): 121 patients (tumors 1–5 cm). Microwave ablation (MWA): 57 patients (tumors 1–3,5 cm). Laser ablation (LA): 45 patients (tumors 1–3,3 cm).
Treatment results. Survival in the RFA group: 1 year – 73,5 %, 2 years – 53,3 %, 3 years – 32,1 %. MWA: 1 year – 78,5 %, 2 years – 63,3 %, 3 years – 58,3 %. LA: 1 year – 88 %, 2 years – 71 %, 3 years – 43,5 %. Median relapse-free survival is 8,5 months. The 1-year survival rate in the subgroup of 12 patients was 84 %. Mortality was 0,6 % (2 cases in the RFA group). The average hospital stay was 7 days.
Conclusion. The use of minimally invasive thermodestruction methods (RFA, MWA, LA) within a multidisciplinary approach significantly expands treatment indications for non-resectable patients (with severe comorbidities, bilobar involvement, low functional liver reserve). This increases overall resectability to 35–40 %, reduces surgical risks and the number of complications, shortens hospitalization times, and improves survival rates.
About the Authors
M. M. TrandofilovRussian Federation
Trandofilov Mikhail Mikhailovich – PhD in medicine, the professor of the Department of Operative Surgery and Topographic Anatomy, the surgeon of the Surgical Department of the University Clinic of the N.A. Semashko Scientific Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
E. N. Prazdnikov
Russian Federation
Prazdnikov Eric Narimanovich – PhD in medicine, professor, the head of the Department of Operative Surgery and Topographic Anatomy
111398, Kuskovskaya 1A str., building 4, Moscow
S. G. Teryasov
Russian Federation
Teryasov Sergey Grigorievich – the assistant of the Department of Operative Surgery and Topographic Anatomy, the surgeon of the Surgical Department of the University Clinic of the N.A. Semashko Scientific Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
D. Yu. Sinyavin
Russian Federation
Sinyavin Dmitry Yuryevich – Oncologist
Moscow, 107076, Matrosskaya Tishina Street, Building 14A
V. P. Shevchenko
Russian Federation
Vadim Pavlovich Shevchenko - MD, Professor, Department of Operative Surgery and Topographic Anatomy; Surgeon, Department of Surgery, University Clinic, N.A. Semashko Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
V. N. Manchurov
Russian Federation
Manchurov Vladimir Nikolaevich – Head of the Department of X-ray Surgical Diagnostic and Treatment Methods at the University Clinic of the N.A. Semashko Scientific Research Institute of Clinical Medicine, Federal State Budgetary Educational Institution of Higher Education, Cand. of Sci. (Med.), Associate Professor of the Department of Cardiology
111398, Kuskovskaya 1A str., building 4, Moscow
A. N. Sizova
Russian Federation
Anna Nikolaevna Sizova – MD, PhD, Associate Professor, Department of Operative Surgery and Topographic Anatomy; Surgeon, Department of Surgery, University Clinic, N.A. Semashko Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
I. A. Koshelev
Russian Federation
Koshelev Igor Andreevich – the assistant of the Department of Operative Surgery and Topographic Anatomy, the head of the 2nd Surgical Department of the University Clinic of the N.A. Semashko Scientific Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
V. S. Vakhromkin
Russian Federation
Vakhromkin Vladimir Sergeevich – the assistant of the Department of Operative Surgery and Topographic Anatomy, the surgeon of the 2nd Surgical Department of the University Clinic of the N.A. Semashko Scientific Institute of Clinical Medicine
111398, Kuskovskaya 1A str., building 4, Moscow
P. G. Shkilnyuk
Russian Federation
Shkilnyuk Petr Gennadievich – physician-therapist, State Budgetary Healthcare Institution
141206, Pushkino, Moscow Region, Aviatsionnaya St., 35
References
1. Kaprin A.D., Starinskiy V.V., Petrova G.V. The state of oncological assistance for the population of Russia in 2021. Moscow: P.A. Herzen Moscow Oncology Research Institute – branch of the Federal State Budgetary Institution "NMITs of Radiology" of the Ministry of Health of the Russian Federation, 2022. (In Russ.)
2. Patyutko Yu.I., Kotelnikov A.G., Polyakov A.N., Chuchuev E.S., Ivanov A.A., Podluzhny D.V., Sagaydak I.V., Shishkina N.A., Mamontov K.G., Agafonova M.G. Surgical tactics in recurrent liver tumors. Bulletin of Surgical Gastroenterology, 2010, № 4, рр. 10–21. (In Russ.)
3. Kosyrev V.U., Dolgushin B.I. Radiofrequency thermoablation in treatment of patients with hepatocellular carcinoma and colorectal cancer liver metastases. Medical Radiology and Radiation Safety, 2011, № 3, рр. 54–61. (In Russ.)
4. De Costanzo G.G., Tortora R.D., Adamo J., De Luca M. Radiofrequency ablation versus laser ablation for the treatment of small hepatocellular carcinoma in cirrhosis: a Randomized Trial. Journal of Gastroenterology and Hepatology, 2015, № 30(3), рр. 59–65. https://doi.org/10.1111/jgh.12791
5. Umberto C., Luciano C. Liver Transplantation and Hepatobiliary surgery. Springer, 2020.
6. Skipenko O.G., Shelygin Yu.A., Achkasov S.I. Metastatic colorectal cancer. M. : Delta Plus, 2020, 360 р.
7. Jiang T, Deng Z, Tian G, Chen F, Bao H, Li J, Wang W. Percutaneous laser ablation: a new contribution to unresectable high-risk metastatic retroperitoneal lesions? Oncotarget., 2017. № 2, рр. 2413–2422. https://doi.org/10.18632/oncotarget.13897
8. Maurizio C. Image-guided Laser Ablation. Springer; 2020.
9. Prazdnikov E.N., Sizova A.N., Svetashov V.S., Zinatulin D.R., Trandofilov M.M., Rudakova M.N., Popov A.Yu., Kostyrev S.V., Prokhorov A.V. Combined treatment of colorectal cancer followed by metastatic liver injury. Journal them. N.I. Pirogova, 2018, № 8, рр. 17–23. (In Russ.) https://doi.org/10.17116/hirurgia201808217
10. Chai W., Zhao Q., Song H.et al. Treatment response and preliminary efficacy of hepatic tumour laser ablation under the guidance of percutaneous and endoscopic ultrasonography. World Journal of Surgical Oncology, 2019, № 17, рр. 133. https://doi.org/10.1186/s12957-0191677-6
Review
For citations:
Trandofilov M.M., Prazdnikov E.N., Teryasov S.G., Sinyavin D.Yu., Shevchenko V.P., Manchurov V.N., Sizova A.N., Koshelev I.A., Vakhromkin V.S., Shkilnyuk P.G. Comparative analysis of treatment of patients with metastatic colorectal cancer using local destruction methods. Moscow Surgical Journal. 2026;(1):116–122. (In Russ.) https://doi.org/10.17238/2072-3180-2026-1-116-122
JATS XML

















