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ARTICLE

Real-World Data on Stage III Non-Small Cell Lung Cancer in Vietnam

Khanh Toan Nguyen1,*, Thi Huong Pham1,2, Van Lam Ngo1, Thi Thuy My Nguyen1, Thi Dao Nguyen1, Khanh Hung Truong1, Van Nhat Nguyen1, Van Thanh Le1, Ba Duc Ho1, Thi Phuong Thao Nguyen1, Thi Ha Phuong Nguyen1, Thi My Linh Dinh1, Thi Hong Anh Vo1, Thi Thuy Phan1, Thi Hai Yen Le1, Thi Nhung Ngo1, Khanh Ha Nguyen1

1 Department of Medical Oncology 2, Nghe An Oncology Hospital, Vinh City, 43000, Vietnam
2 Department of Oncology, Hanoi Medical University, Ha Noi City, 10000, Vietnam

* Corresponding Author: Khanh Toan Nguyen. Email: email

(This article belongs to the Special Issue: Novel Biomarkers and Treatment Strategies in Solid Tumor Diagnosis, Progression, and Prognosis)

Oncology Research 2025, 33(12), 4013-4028. https://doi.org/10.32604/or.2025.069281

Abstract

Objective: Patients with stage III non-small cell lung cancer (NSCLC) present with a heterogeneous disease profile and often require multifaceted treatment strategies. This research aimed to investigate the demographic features, therapeutic patterns, and survival outcomes of such patients in Vietnam. Methods: A retrospective descriptive study was conducted on 731 patients diagnosed with stage III NSCLC American Joint Committee on Cancer (AJCC) 8th edition, at Nghe An Oncology Hospital from January 2018 to August 2024. Descriptive statistics summarized baseline and treatment characteristics. We calculated progression-free survival (PFS) and overall survival (OS) through the Kaplan–Meier approach and compared survival curves with the log-rank test. Prognostic variables were assessed using Cox regression analysis. Results: Patients had a median age of 64 years, and the majority (84%) were male. Disease stages IIIA, IIIB, and IIIC accounted for 26.0%, 49.9%, and 24.1% of cases, respectively. Adenocarcinoma (60.7%) was the most common histological subtype. Initial treatments included surgery (8.5%), concurrent chemoradiotherapy (38.6%), sequential chemoradiotherapy (2.2%), radiotherapy alone (1.4%), systemic therapy (37.3%), and palliative care (12.0%). From 2018 to 2024, the use of systemic therapy declined (88.5% to 21.7%), while concurrent chemoradiotherapy rose significantly (1.1% to 51.5%). Median progression-free survival (mPFS) and median overall survival (mOS) were 8.9 months and 20.5 months, respectively. Patients with stage IIIA had significantly better outcomes (mPFS: 12.6 months; mOS: 32.4 months; p < 0.001). Surgical treatment yielded the longest survival (mPFS: 13.5 months; mOS: 42.8 months). Favorable prognostic factors included adenocarcinoma subtype, presence of driver mutations, stage IIIA, and good performance status. Conclusion: For stage III NSCLC, concurrent chemoradiotherapy is still considered the standard treatment, whereas surgery can provide the highest survival advantage in carefully selected cases. Histology, molecular profile, and disease stage are key prognostic indicators.

Keywords

Non-small cell lung cancer; stage III; surgery; concurrent chemoradiotherapy; immunotherapy

Supplementary Material

Supplementary Material File

Cite This Article

APA Style
Nguyen, K.T., Pham, T.H., Ngo, V.L., Nguyen, T.T.M., Nguyen, T.D. et al. (2025). Real-World Data on Stage III Non-Small Cell Lung Cancer in Vietnam. Oncology Research, 33(12), 4013–4028. https://doi.org/10.32604/or.2025.069281
Vancouver Style
Nguyen KT, Pham TH, Ngo VL, Nguyen TTM, Nguyen TD, Truong KH, et al. Real-World Data on Stage III Non-Small Cell Lung Cancer in Vietnam. Oncol Res. 2025;33(12):4013–4028. https://doi.org/10.32604/or.2025.069281
IEEE Style
K. T. Nguyen et al., “Real-World Data on Stage III Non-Small Cell Lung Cancer in Vietnam,” Oncol. Res., vol. 33, no. 12, pp. 4013–4028, 2025. https://doi.org/10.32604/or.2025.069281



cc Copyright © 2025 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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