Expanding horizons in lung cancer immunotherapy
Immunotherapy continues to transform the management of non-small cell lung cancer (NSCLC), offering the prospect of long-term survival even to patients at advanced stages of the disease. According to data presented at the 29th Russian Oncology Congress, one in four patients (27.8%) with metastatic squamous NSCLC remains alive five years after initiation of camrelizumab-based chemoimmunotherapy[1].
Experts emphasized that the advent of checkpoint inhibitors has fundamentally reshaped the treatment paradigm for advanced lung cancer. Today, one of these agents — camrelizumab — has become available to Russian patients.
Lung cancer remains one of the most devastating cancers in Russia. Each year, more than 50,000 new cases are diagnosed, with 69.5% of patients identified at stages III–IV[2]. Globally, lung cancer ranks first in incidence and mortality among malignant neoplasms[3], and prognosis remains poor. In Russia, almost half of patients (44.3%) die within the first year after diagnosis[2].
.Efficacy of camrelizumab was confirmed in the CAMELsq study, where adding the agent to first-line treatment in patients with squamous NSCLC resulted in an overall survival benefit across all subgroups, regardless of PD-L1 expression level[1]. Notably, 84% of patients who completed a full two-year course of treatment surpassed the five-year survival threshold, allowing lung cancer in these cases to be viewed not as a fatal disease, but as a potentially chronic condition[1],[5].
On 9 December, the Ministry of Health of the Russian Federation approved a new indication for Areima® (camrelizumab) as first-line treatment for NSCLC. In addition to the squamous histological subtype, the indication also includes lung adenocarcinoma[4].
Camrelizumab mode of action is particularly interesting at the molecular level. In addition to PD-1 blockade, the antibody can bind to ULBP2, a protein involved in regulating natural killer (NK) cell activity. This effect enhances antitumor immune responses and reduces dependence of clinical outcomes on PD-L1 expression levels[7],[8],[9],[10].
Camrelizumab is also actively used and studied in esophageal cancer, one of the most aggressive malignancies, ranking seventh worldwide in cancer-related mortality[13]. In Russia, approximately 7,200 new cases of esophageal cancer are diagnosed annually, with more than 60% detected at stages III–IV[2].
The ESCORT-1st study demonstrated that adding camrelizumab to first-line chemotherapy for locally advanced or metastatic squamous cell esophageal cancer doubles three-year overall survival compared with standard chemotherapy alone[14].
To date, camrelizumab is being investigated in more than 400 clinical trials worldwide for the treatment of various malignancies, including nasopharyngeal carcinoma, esophageal, gastric, hepatic, and lung cancers, among others[15]. Mounting evidence supports further expansion of indications, opening new therapeutic opportunities for Russian physicians and patients.
1 Camel Sq. Caicun Zhou, et al. 2025 ELCC # 12P
2 Kaprin A.D., Starinsky V.V., Shakhzadova A.O. (eds.). The State of Cancer Care for the Population of Russia in 2024. Moscow: P.A. Herzen Moscow Oncology Research Institute — branch of the National Medical Research Center of Radiology, Ministry of Health of Russia; 2025. 275 p. (in Russian).
3Ferlay J, Ervik M, Lam F, Laversanne M, Colombet M, Mery L, Piñeros M, Znaor A, Soerjomataram I, Bray F (2024). Global Cancer Observatory: Cancer Today. Lyon, France: International Agency for Research on Cancer. Available from: https://gco.iarc.who.int/today, accessed [19.12.2025].
4Instructions for medical use of AREIMA® (camrelizumab). Marketing Authorization No. (007636)-(RG-RU) dated 09.12.2025. Available at: https://grls.rosminzdrav.ru/Grls_View_v2.aspx?routingGuid=9fa2cb13-d2d3-4067-ad38-cc5d5771080d. Accessed: 19.02.2025.
5Сamel Sq. Zhou et al., 2021 Journal of Thoracic Oncology.
6Camel. Zhou, et al., 2024 Journal for Immuno Therapy of Cancer.
7Yamaguchi et al. Cancer Sci. 2012 Jul 10;103(8):1405–1413. doi: 10.1111/j.1349-7006.2012.02330.
8Lopez-Larrea C., Suarez-Alvarez B., Lopez-Soto A., Lopez-Vazquez A., Gonzalez S. (2008). The NKG2D receptor: sensing stressed cells. Trends Mol. Med. 14, 179-189.
9Nausch N., Cerwenka A. (2008). NKG2D ligands in tumor immunity. Oncogene 27, 5944-5958.
10 L. Fernandez-Messina et al., Differential mechanisms of shedding of the glycosylphosphatidylinositol (GPI)-anchored NKG2D ligands, J. Biol. Chem. 285 (12) (2010) 8543–8551.
11 Liu, R., Oldham, R. J., Teal, E., Beers, S. A., & Cragg, M. S. (2020). Fc-Engineering for Modulated Effector Functions-Improving Antibodies for Cancer Treatment. Antibodies (Basel, Switzerland), 9(4), 64. https://doi.org/10.3390/antib9040064
12Wu, J. D., Atteridge, C. L., Wang, X., Seya, T., Plymate, S. R. (2009). Obstructing shedding of the immunostimulatory MHC class I chain-related gene B prevents tumor formation. Clinical cancer research : an official journal of the American Association for Cancer Research, 15(2), 632–640. https://doi.org/10.1158/1078-0432.CCR-08-1305 3, https://www.neb-online.fr/en/glycobiology/glycosidases/ Protein Deglycosylation Mix
13Ferlay J, Ervik M, Lam F, Laversanne M, Colombet M, Mery L, Piñeros M, Znaor A, Soerjomataram I, Bray F (2024). Global Cancer Observatory: Cancer Today. Lyon, France: International Agency for Research on Cancer. Available from: https://gco.iarc.who.int/today, accessed [19.12.2025].
14Mingming He, et al. Final analysis of camrelizumab plus chemotherapy for untreated advanced or metastatic esophageal squamous cell carcinoma: The ESCORT-1st trial, Med, Volume 5, Issue 9, 2024, Pages 1137-1149.e3, ISSN 2666-6340, https://doi.org/10.1016/j.medj.2024.05.008.
15https://clinicaltrials.gov/