

Experience of using lenvatinib in the treatment of hepatocellular cancer at the Republican Oncology Center of the Republic of North Ossetia-Alania in 2018–2022. Balance of efficiency and accessibility in regional practice
https://doi.org/10.33667/2078-5631-2024-17-49-52
Abstract
The overall incidence of liver cancer in the Republic of North Ossetia-Alania has remained stable over the past five years. Moreover, the initial diagnostic of HCC occurs at widespread stage, which limits the possibilities of cured therapy. The Republican Oncology Clinic has accumulated experience in using the drug lenvatinib for advanced and metastatic hepatocellular cancer. In the realities of a small regional dispensary, and has to find a balance between efficiency and availability of therapeutic options to provide effective therapy for all patients. The authors conducted a single-center retrospective analysis of the effectiveness and safety of lenvatinib in real clinical practice in patients with hepatocellular cancer at the Republican Oncology Center of the Republic of North Ossetia Alania. The analysis included 18 patients with HCC who received lenvatinib monotherapy. 11(61%) patients had concomitant viral hepatitis B or C, 15 (83%) had distant metastases to the lymph nodes, lungs, adrenal glands or other organs. A feature of this patient population is the long period of time from the prescription of drug therapy for HCC to its actual start – on average 46 days, with a range from 5 to 100 days. We believe that a delay in initiating therapy may affect the results obtained. Median PFS in 1st line of lenvatinib therapy was 10.1 months (2.3 months to 13.1 months). Median PFS2 (defined as the time from 1st line treatment on lenvatinib to progression on first subsequent therapy) was 19.1 months. 6 (33%) patients received lenvatinib in the second line after progression on another drug therapy. The median second-line PFS in this case was 5.9 months (3.8 months‑7.7 months). Lenvatinib had a manageable and predictable tolerability profile. No new safety signals were identified.
Conclusion: The use of lenvatinib as monotherapy in adult patients with advanced or unresectable hepatocellular carcinoma has proven to be an effective strategy that balances clinical benefit and availability of the drug.
About the Authors
M. B. BolievaRussian Federation
Bolieva Marina B.- oncologist, head of Outpatient Chemotherapy Dept
Vladikavkaz
A. A. Yepkhiev
Russian Federation
Yepkhiev Alexander A. - PhD Med, head of Dept of Pathological Anatomy with Forensic Medicine
Vladikavkaz
L. M. Voronkova
Russian Federation
Voronkova Liya M. - oncologist, head of Inpatient Chemotherapy Dept
Vladikavkaz
G. E. Zangionov
Russian Federation
Zangionov Georgy E. - oncologist at Outpatient Chemotherapy Dep
Vladikavkaz
References
1. Malignant tumors in Russia in 2021 (morbidity and mortality) / ed. HELL. Kaprin, V.V. Starinsky, A.O. Shakhzadov. M.: MNIOI im. P.A. Herzen – branch of the Federal State Budgetary Institution «National Medical Research Center of Radiology» of the Ministry of Health of Russia, 2022. 252 p.
2. Malignant tumors in Russia in 2022 (morbidity and mortality) / ed. Kaprin, V.V. Starinsky, A.O. Shakhzadov. M.: MNIOI im. P.A. Herzen is a branch of the Federal State Budgetary Institution «National Medical Research Center of Radiology» of the Ministry of Health. Russia, 2023. 275 p.: ill.
3. Atezolizumab plus Bevacizumab in Unresectable Hepatocellular Carcinoma.Richard S. Finn, M.D., Shukui Qin, M.D., Masafumi Ikeda, M.D., Peter R. Galle, M.D., Michel Ducreux, M.D., Tae-You Kim, M.D., Masatoshi Kudo, M.D., Valeriy Breder, M.D., Philippe Merle, M.D., Ahmed O. Kaseb, M.D., Daneng Li, M.D., Wendy Verret, Ph.D., et al. For the IMbrave150 Investigators* N Engl. J. Med. 2020; 382: 1894–1905. DOI: 10.1056/NEJMoa1915745
4. Clinical recommendations. Liver cancer (hepatocellular). International Statistical Classification of Diseases and Related Health Problems coding: C22.0. Year of approval: 2022. Age category: Adults. Revision no later than: 2024. https://cr.minzdrav.gov.ru/
5. Kudo M, Finn RS, Qin S. et al. Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial. Lancet. 2018; 391 (10126): 1163–1173. DOI: 10.1016/S0140–6736(18)30207–1
6. Casadei-Gardini A, Rimini M, Kudo M. et al. Real Life Study of Lenvatinib Therapy for Hepatocellular Carcinoma: RELEVANT Study. Liver Cancer. 2022; 11 (6): 527–539. Published 2022 Jul 11. DOI: 10.1159/000525145
7. Oken M.M., Creech R.H., Davis T.E. Toxicology and response criteria of the Eastern Cooperative Oncology Group. Am.J. Clin. Oncol. Cancer Clin. Trials. 1982; 5 (6): 649–655.
8. Characteristics of the drug lenvatinib. https://eisai.ru/instructions/lenvima-ohlp/
9. Lencioni R., Llovet J.M. ModifiedRECIST (mRECIST) assessment for hepatocellular carcinoma. Seminars in Liver Disease. 2010; 30 (1): 52–60.
10. Ivashkin V.T., Mayevskaya M.V., Zharkova M.S., Zhigalova S.B., Kitsenko E.A., Manukyan G.V., Trukhmanov A.S., Maev I.V., Tikhonov I N., Deeva T.A. Clinical recommendations of the Russian Society for the Study of the Liver and the Russian Gastroenterological Association for the diagnosis and treatment of fibrosis and cirrhosis of the liver and their complications. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2021; 31 (6): 56–102. https://doi.org/10.22416/1382–4376–2021–31–6–56–102
11. Rimini M, Rimassa L, Ueshima K, et al. Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis. ESMO Open. 2022; 7 (6): 100591. DOI: 10.1016/j.esmoop.2022.100591
Review
For citations:
Bolieva M.B., Yepkhiev A.A., Voronkova L.M., Zangionov G.E. Experience of using lenvatinib in the treatment of hepatocellular cancer at the Republican Oncology Center of the Republic of North Ossetia-Alania in 2018–2022. Balance of efficiency and accessibility in regional practice. Medical alphabet. 2024;(17):49-52. (In Russ.) https://doi.org/10.33667/2078-5631-2024-17-49-52