Preview

Meditsinskiy sovet = Medical Council

Advanced search

Remote results of treatment of patients of the Russian population with stage I–II non-small cell lung cancer (results of the observational study CARL-001)

https://doi.org/10.21518/ms2025-096

Abstract

Introduction. This paper examines the treatment outcomes for patients with stage I and II non-small cell lung cancer (NSCLC) in real clinical practice. The frequency of molecular genetic testing of operated patients was determined, and long-term prognoses for the disease were determined depending on the volume of treatment.

Aim. To determine the effect of adding adjuvant treatment to radical surgery on the treatment outcomes in real clinical practice – overall and relapse-free survival. To determine the frequency and results of molecular genetic testing in patients with stage I–II NSCLC.

Materials and methods. The results were obtained during the study – clinical approbation of lung cancer (CARL-001). The study included 401 patients with stage I–IIB NSCLC. The study included 129 women and 272 men. The median age was 56 years. There were 272 patients with stage I disease, 129 with stage II. 83 patients received combined treatment, 318 patients received only surgical treatment. The median follow-up was 36 months.

Results. PD-L1 testing was performed in 31.7% of patients with stage II and in 14% of patients with stage I. The frequency of testing for mutations in the EGFR and ALK genes was 53.6% and 17.0% for stage II and 46% and 14.8% for stage I, respectively. Three-year overall survival of patients with stage IIA and adjuvant chemotherapy was higher compared to stage IIA patients who did not receive adjuvant treatment – 65% vs 69.24%. A similar indicator in patients with stage IIB also showed an advantage from adjuvant treatment 57.69% vs 72.86% in favor of those who received adjuvant. In patients with stage IIA and adjuvant therapy, 3-year relapse-free survival was 53.86% versus 50.0% without adjuvant. Among patients with stage IIB, the same parameter was 53.85% in the group without adjuvant versus 65.71% in the group that received adjuvant therapy.

Conclusions. Adjuvant polychemotherapy in patients with stage II disease has a positive effect on long-term treatment outcomes in the form of increased overall and relapse-free survival compared to patients with a similar stage of the disease without adjuvant treatment. Molecular genetic testing of patients with NSCLC allows us to identify the presence of activating mutations and PD-L1 expression, which is important information for planning further treatment tactics.

About the Authors

K. K. Laktionov
Blokhin National Medical Research Center of Oncology; Pirogov Russian National Research Medical University
Russian Federation

Konstantin K. Laktionov, Dr. Sci. (Med.), First Deputy Director, Head of the Department of Antitumor Drug Therapy No. 3, Department of Drug Treatment; Professor of the Department of Oncology and Radiation Therapy Institute of Surgery

24, Kashirskoye Shosse, Moscow, 115478; 
1, Ostrovityanov St., Moscow, 117997



V. V. Breder
Blokhin National Medical Research Center of Oncology
Russian Federation

Valeriy V. Breder, Dr. Sci. (Med.), Head of the Department of Drug Treatment

24, Kashirskoye Shosse, Moscow, 115478



A. K. Allakhverdiev
Loginov Moscow Clinical Scientific Center
Russian Federation

Arif K. Allakhverdiev, Dr. Sci. (Med.), Head of the Department of Thoracoabdominal Surgery

1, Bldg. 1, Novogireevskaya St., Moscow, 111123



A. M. Kazakov
Blokhin National Medical Research Center of Oncology
Russian Federation

Aleksey M. Kazakov, Cand. Sci. (Med.), Oncologist of the Department of Antitumor Drug Therapy No. 3, Department of Drug Treatment

24, Kashirskoye Shosse, Moscow, 115478



A. E. Gorokhov
Blokhin National Medical Research Center of Oncology
Russian Federation

Arthur E. Gorokhov, Dr. Sci. (Med.), Oncologist of the Department of Antitumor Drug Therapy No. 3, Drug Treatment Department

24, Kashirskoye Shosse, Moscow, 115478



P. V. Kononets
Blokhin National Medical Research Center of Oncology
Russian Federation

Pavel V. Kononets, Dr. Sci. (Med.), Director of the N.N. Trapeznikov Research Institute of Oncology, Head of the Department of Thoracic Oncology, Department of Abdominal Oncology No. 1

24, Kashirskoye Shosse, Moscow, 115478



D. I. Yudin
Blokhin National Medical Research Center of Oncology
Russian Federation

Denis I. Yudin, Cand. Sci. (Med.), Senior Researcher, Department of Antitumor Drug Therapy No. 3, Drug Treatment Department

24, Kashirskoye Shosse, Moscow, 115478



D. L. Stroyakovsky
Moscow City Oncology Hospital No. 62
Russian Federation

Daniil L. Stroyakovskiy, Cand. Sci. (Med.), Head of the Chemotherapy Department

27, Bldg. 1–30, Krasnogorsk, Istra, Moscow Region, 143515



Ya. S. Akhmadiyarova
Moscow City Oncology Hospital No. 62
Russian Federation

Yana S. Akhmadiyarova, Oncologist of the Chemotherapy Department

27, Bldg. 1–30, Krasnogorsk, Istra, Moscow Region, 143515



V. V. Kozlov
Novosibirsk Regional Oncology Clinical Dispensary; Novosibirsk State Medical University
Russian Federation

Vadim V. Kozlov, Dr. Sci. (Med.), Head of Department No. 3; Assistant, Department of Oncology

2, Plakhotnov St., Novosibirsk, 630108; 
52, Krasny Ave., Novosibirsk, 630091



A. M. Fedun
Research Institute of Clinical Oncology “Nizhny Novgorod Regional Clinical Oncology Dispensary”
Russian Federation

Andrey M. Fedun, Cand. Sci. (Med.), Head of the 8th  Oncology Department of Thoracic Oncology

11/1, Delovaia St., Nizhny Novgorod, 603163



T. F. Ibragimov
Podolsk City Clinical Hospital
Russian Federation

Timur F. Ibragimov, Cand. Sci. (Med.), Head of the Surgical Department of Thoracoabdominal Oncology

38, Bldg. 18, Kirov St., Podolsk, Moscow Region, 142110



T. A. Sannikova
Perm Regional Clinical Hospital
Russian Federation

Tatyana A. Sannikova, Oncologist

85, Pushkin St., Perm, 614990



I. V. Plokhotenko
Clinical Oncology Dispensary
Russian Federation

Irina V. Plokhotenko, Oncologist

9, Bldg. 1, Zavertyaev St., Omsk, 644013



References

1. Kratzer TB, Bandi P, Freedman ND, Smith RA, Travis WD, Jemal A, Siegel RL. Lung cancer statistics, 2023. Cancer. 2024;130(8):1330−1348. https://doi.org/10.1002/cncr.35128.

2. Каприн АД, Старинский ВВ, Шахзадовой АО (ред.). Злокачественные новообразования в России в 2021 году. М.: МНИОИ им. П.А. Герцена − филиал ФГБУ «НМИЦ радиологии» Минздрава России; 2022. 252 с. Режим доступа: https://oncology-association.ru/wp-content/uploads/2022/11/zlokachestvennye-novoobrazovaniya-v-rossii-v-2021-g_zabolevaemost-i-smertnost.pdf.

3. de Groot PM, Wu CC, Carter BW, Munden RF. The epidemiology of lung cancer. Transl Lung Cancer Res. 2018;7(3):220−233. https://doi.org/10.21037/tlcr.2018.05.06.

4. Garinet S, Wang P, Mansuet-Lupo A, Fournel L, Wislez M, Blons H. Updated Prognostic Factors in Localized NSCLC. Cancers. 2022;14(6):1400. https://doi.org/10.3390/cancers14061400.

5. Mueller M. ED08.01 Surgery of Early-Stage NSCLC. J Thorac Oncol. 2017;12(1):S40−S42. https://doi.org/10.1016/j.jtho.2016.11.038.

6. McDonald F, De Waele M, Hendriks LE, Faivre-Finn C, Dingemans AC, Van Schil PE. Management of stage I and II nonsmall cell lung cancer. Eur Respir J. 20173;49(1):1600764. https://doi.org/10.1183/13993003.00764-2016.

7. Raman V, Yang CJ, Deng JZ, D’Amico TA. Surgical treatment for early stage non-small cell lung cancer. J Thorac Dis. 2018;10(Suppl. 7):S898−S904. https://doi.org/10.21037/jtd.2018.01.172.

8. Veronesi G, Novellis P, Voulaz E, Alloisio M. Robot-assisted surgery for lung cancer: State of the art and perspectives. Lung Cancer. 2016;101:28−34. https://doi.org/10.1016/j.lungcan.2016.09.004.

9. Lackey A, Donington JS. Surgical management of lung cancer. Semin Intervent Radiol. 2013;30(2):133–140. https://doi.org/10.1055/s-0033-1342954.

10. Arriagada R, Bergman B, Dunant A, Le Chevalier T, Pignon JP, Vansteenkiste J. Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer. N Engl J Med. 2004;350(4):351−360. https://doi.org/10.1056/NEJMoa031644.

11. Kim MH, Kim SH, Lee MK, Eom JS. Recent Advances in Adjuvant Therapy for Non-Small-Cell Lung Cancer. Tuberc Respir Dis. 2024;87(1):31−39. https://doi.org/10.4046/trd.2023.0085.

12. Pignon JP, Tribodet H, Scagliotti GV, Douillard JY, Shepherd FA, Stephens RJ et al. Lung adjuvant cisplatin evaluation: a pooled analysis by the LACE Collaborative Group. J Clin Oncol. 2008;26(21):3552−3559. https://doi.org/10.1200/JCO.2007.13.9030.

13. Rotolo F, Dunant A, Le Chevalier T, Pignon JP, Arriagada R. Adjuvant cisplatin-based chemotherapy in nonsmall-cell lung cancer: new insights into the effect on failure type via a multistate approach. Ann Oncol. 2014;25(11):2162–2166. https://doi.org/10.1093/annonc/mdu442.

14. Felip E, Altorki N, Zhou C, Csőszi T, Vynnychenko I, Goloborodko O et al. Adjuvant atezolizumab after adjuvant chemotherapy in resected stage IB-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase 3 trial. Lancet. 2021;398(10308):1344−1357. https://doi.org/10.1016/S0140-6736(21)02098-5.

15. Wakelee HA, Altorki NK, Zhou C, Csőszi T, Vynnychenko IO, Goloborodko O et al. IMpower010: Final disease-free survival (DFS) and second overall survival (OS) interim results after ≥5 years of follow up of a phase III study of adjuvant atezolizumab vs best supportive care in resected stage IB-IIIA non-small cell lung cancer (NSCLC). J Clin Oncol. 2024;42(17):LBA8035. https://doi.org/10.1200/JCO.2024.42.17_suppl.LBA803.

16. Cascone T, Awad MM, Spicer J, He J, Lu S, Sepesi B et al. LBA1 CheckMate 77T: Phase III study comparing neoadjuvant nivolumab (NIVO) plus chemotherapy (chemo) vs neoadjuvant placebo plus chemo followed by surgery and adjuvant NIVO or placebo for previously untreated, resectable stage II–IIIb NSCLC. Ann Oncol. 2023;34(Suppl. 2):S1295. https://doi.org/10.1016/j.annonc.2023.10.050.

17. Oselin K, Shim BY, Okada M, Bryl M, Bonanno L, Demirag G. Pembrolizumab vs placebo for early-stage non‒small-cell lung cancer after resection and adjuvant therapy: Subgroup analysis of patients who received adjuvant chemotherapy in the phase 3 PEARLS/ KEYNOTE-091 study. J Clin Oncol. 2023;41(16):8520. https://doi.org/10.1200/JCO.2023.41.16_suppl.8520.

18. Tsuboi M, Herbst RS, John T, Kato T, Majem M, Grohé C et al. Overall Survival with Osimertinib in Resected EGFR-Mutated NSCLC. N Engl J Med. 2023;389(2):137−147. https://doi.org/10.1056/NEJMoa2304594.

19. Wu YL, Dziadziuszko R, Ahn JS, Barlesi F, Nishio M, Lee DH et al. Alectinib in Resected ALK-Positive Non–Small-Cell Lung Cancer. N Engl J Med. 2024;390(14):1265–1276. https://doi.org/10.1056/NEJMoa2310532.

20. Kim MH, Kim SH, Lee MK, Eom JS. Recent Advances in Adjuvant Therapy for Non-Small-Cell Lung Cancer. Tuberc Respir Dis. 2024;87(1):31–39. https://doi.org/10.4046/trd.2023.0085.


Review

For citations:


Laktionov KK, Breder VV, Allakhverdiev AK, Kazakov AM, Gorokhov AE, Kononets PV, Yudin DI, Stroyakovsky DL, Akhmadiyarova YS, Kozlov VV, Fedun AM, Ibragimov TF, Sannikova TA, Plokhotenko IV. Remote results of treatment of patients of the Russian population with stage I–II non-small cell lung cancer (results of the observational study CARL-001). Meditsinskiy sovet = Medical Council. 2025;(10):112-119. (In Russ.) https://doi.org/10.21518/ms2025-096

Views: 217


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2079-701X (Print)
ISSN 2658-5790 (Online)