Prognostic Significance of the Maximum Standardized Uptake Value on the Prognosis of Clinical Stage IA Lung Adenocarcinoma Based on the 8th Edition TNM Classification
Background There are few reports on the utility of the maximum standardized uptake value (SUVmax) for predicting the prognosis of early-stage lung adenocarcinoma based on the latest tumor-node-metastasis (TNM) classification. This study aimed to determine whether clinicopathologic factors, including...
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Veröffentlicht in: | Annals of surgical oncology 2023-02, Vol.30 (2), p.830-838 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
There are few reports on the utility of the maximum standardized uptake value (SUVmax) for predicting the prognosis of early-stage lung adenocarcinoma based on the latest tumor-node-metastasis (TNM) classification. This study aimed to determine whether clinicopathologic factors, including the SUVmax, affect prognosis in these patients.
Patients and Methods
We enrolled 527 patients with c-stage IA lung adenocarcinoma who underwent lobectomy or greater resection between 2011 and 2017. Recurrence-free survival (RFS) and overall survival (OS) were analyzed using Kaplan–Meier curves and compared using the log-rank test. Factors associated with RFS and OS were determined using the Cox proportional hazards model.
Results
RFS was significantly different based on tumor stage. In contrast, there was no significant difference in OS between patients with stage IA2 and IA3 disease (
p
= 0.794), although there were significant differences in OS between patients with stage IA1 and IA2 disease (
p
= 0.024) and between patients with stage IA1 and IA3 disease (
p
= 0.012). Multivariate analysis demonstrated that SUVmax was independently associated with both RFS and OS among patients with c-stage IA lung adenocarcinoma (RFS,
p
= 0.017; OS,
p
= 0.047). Further, even though there was no significant difference in OS between patients with stage IA2 and IA3 disease (
n
= 410), SUVmax was able to stratify patients with high and low RFS and OS among these patients (RFS,
p
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ISSN: | 1068-9265 1534-4681 |
DOI: | 10.1245/s10434-022-12684-w |