Abstract
Objectives
To investigate the role of PET in predicting the prognosis of resected stage IA non-small cell lung cancer (NSCLC) and planning individualized therapeutic strategies.
Methods
We retrospectively reviewed the data of patients who underwent surgical resection for lung cancer between January 2004 and December 2014. The clinical data, imaging characteristics of nodules, surgical approaches, and outcomes were analyzed.
Results
We evaluated 998 cases; 637 patients with pathological stage I disease were categorized as follows: stage IA1 (251 cases), stage IA2 (250 cases), and stage IA3 (136 cases). The mean follow-up period was 109 months. Significant differences were observed in sex, tumor differentiation, epidermal growth factor receptor mutation, smoking habits, lymphovascular space invasion, tumor size, maximum standard uptake value (SUVmax), and carcinoembryonic antigen level among the groups. Multivariable Cox regression revealed that ground-glass opacity ratio (hazard ratio (HR) = 0.001) and tumor SUVmax independently predicted the postoperative risk of relapse for stage IA3 NSCLC. The HR for SUVmax > 4 was 8.986 (p < 0.001). The 5-year overall survival (OS) rates were 87.2%, 92.9%, and 82.7%, and the 5-year disease-free survival (DFS) rates were 93.2%, 84.2%, and 70.51% for stage IA1, IA2, and IA3 NSCLC, respectively (both p < 0.001). OS and DFS rates were poor in stage IA3 NSCLC patients with an SUVmax uptake > 4 (OS, 71.0% and 92.2%; DFS, 50.2% and 87.3%, for SUVmax > 4 and ≤ 4, respectively; both p = 0.001).
Conclusions
SUVmax was a prognostic factor for resected stage IA NSCLC. Postoperative treatment may be considered for IA3 NSCLC with SUVmax > 4.
Key Points
• PET helps surgeons to assess patients with early-stage lung cancer.
• This retrospective study revealed that PET plays an influential role in predicting the prognosis of resected lung cancer.
• Better prognostication aids better planning of therapeutic strategies with diversification.
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Change history
30 March 2021
The countries in affiliations 1 and 2 were presented incorrectly.
13 July 2021
A Correction to this paper has been published: https://doi.org/10.1007/s00330-021-08158-4
Abbreviations
- CEA:
-
Carcinoembryonic antigen
- CI:
-
Confidence interval
- DFS:
-
Disease-free survival
- ECOG:
-
Eastern Cooperative Oncology Group of Performance Status
- EGFR:
-
Epidermal growth factor receptor
- GGO:
-
Ground-glass opacity
- HR:
-
Hazard ratio
- LN:
-
Lymph node
- LVSI:
-
Lymphovascular space invasion
- NCCN:
-
National Comprehensive Cancer Network
- NSCLC:
-
Non-small cell lung cancer
- OS:
-
Overall survival
- SCC:
-
Squamous cell carcinoma
- SUVmax:
-
Maximum standardized uptake value
- TNM:
-
Tumor–Node–Metastasis
- VPI:
-
Visceral pleural invasion
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Acknowledgements
We thank the support we received from the members of the Cancer Registry Group, Tri-Service General Hospital.
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The scientific guarantor of this publication is Tsai-Wang, Huang.
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No complex statistical methods were necessary for this paper.
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Written informed consent was not required for this study because it’s a retrospective observational study from the single-center database which has been certificated by the institutional Review Board/Ethics Committee of National Defense Medical Center, Tri-service general hospital.
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• retrospective
• observational
• performed at one institution
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The original online version of this article was revised: Several values in table 3 were incorrect.
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Chou, HP., Lin, KH., Huang, HK. et al. Prognostic value of positron emission tomography in resected stage IA non-small cell lung cancer. Eur Radiol 31, 8021–8029 (2021). https://doi.org/10.1007/s00330-021-07801-4
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DOI: https://doi.org/10.1007/s00330-021-07801-4