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].

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"The availability of immunotherapy has given patients with metastatic lung cancer the opportunity to live longer,"
emphasized Fedor V. Moiseenko, Doctor of Medical Sciences, Head of the Department of Oncology Chemotherapy and Biotherapy at the N.P. Napalkov St. Petersburg Clinical Research Center for Specialized Types of Medical Care (Oncology).

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].

"According to the CameL study[6], the use of camrelizumab in patients with stage IIIB—IV non-squamous NSCLC significantly increases five-year overall survival — up to 31.2%, compared with 19.3% in the standard chemotherapy group,"
noted F. V. Moiseenko. Among patients who received camrelizumab for two years, nearly one in two (46.5%) maintained a response to therapy even after five years[5],[6].

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].

"Structural features of camrelizumab molecular design ensure its high affinity and lower susceptibility to the body’s immune responses. These properties contribute to therapeutic efficacy, favorably comparing from earlier generation checkpoint inhibitors,[11],[12]"
explained Anastasia S. Danilova, Head of the Day Care Unit, Moscow City Oncology Hospital No. 62.

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/
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