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Letters to the Editor |
a Department of Cardiovascular and Thoracic Surgery, Cliniques universitaires St-Luc-UCL, Brussels, Belgium
b Department of Nuclear Medicine, Cliniques universitaires St-Luc-UCL, Brussels, Belgium
Received 3 July 2008; accepted 14 July 2008.
* Corresponding author. Address: Cardio-Vascular and Thoracic Surgery Unit, U.C.L. Saint Luc Hospital, Université catholique de Louvain, Avenue Hippocrate 10, B-1200 Brussels, Belgium. Tel.: +32 2 7646107; fax: +32 2 7648960. (Email: Poncelet{at}chir.ucl.ac.be).
Key Words: Non-small cell lung cancer PET-FDG SUV Prognosis Thoracic surgery
We very much appreciated the remarks and comments from Chong [1] on our recently published results on the prognostic significance of PET-FDG SUVmax in early stage non-small cell lung cancer [2].
In his letter to the editor, Chong has underlined several potential faults with data presentation and analysis that we would like to answer for the sake of clarity even though a peer reviewed statistical analysis did validate the current published study.
Chong rightly stated that our article did not provide the results of the univariate analysis of pre-defined prognostic factors for survival.
None of the following variables reached the level of significance and therefore, were not mentioned in the final revised manuscript: grade of differentiation (HR 2.06; 95%CI [0.98–4.3]), histology (HR 0.53; 95%CI [0.27–1.04]), N status (HR 1.6; 95%CI [0.8–3.24]), sex (HR 1.2; 95%CI [0.57–2.4]).
As suggested by Chong, a multivariate analysis including all variables with a level of significance < or =0.10 was conducted. Again, SUVmax greater than 7.8 was the only significant (p = 0.009) variable with an HR 2.6 (95%CI [1.3–5.4]).
The median survival time was chosen for differentiating groups, but obviously, all Kaplan–Meier survival curves were generated at the same time. The overall survival (OS) at five-year for the SUVlow and the SUVhigh groups were 82.2% and 50.2% (log-rank p = 0.001).
The disease-free survival (DFS) at five-year for the SUVlow and the SUVhigh groups were 77% and 60.7%, respectively (log-rank p = 0.019).
No cancer-related deaths were present in both SUV groups and we thought this would not bias the analysis. However, as suggested, we here have excluded from all analysis the patients who died of a cancer-unrelated death during the follow-up (n = 21). For this selected subgroup, OS at five-year for the SUVlow and the SUVhigh groups were 88.3% and 65.7% (log-rank p = 0.001) and DFS at five-year for the SUVlow and the SUVhigh groups were 81.7% and 55%, respectively (log-rank p = 0.007).
We further dichotomised our patients based on the median age (65.3 years old) and did not find significant differences in survival (log-rank p = 0.22).
Finally, we can only disagree with Chong's conclusion stating that SUV does not provide additional clinically relevant information compare to pTNM staging alone as several contemporary studies on lung cancers have supported our conclusions [3,4]. In the Sloan-Memorial series [5], Downey et al. included all stage I to stage IV patients for statistical analysis and the subanalysis on early stage tumors was performed with a SUVmax cut-off (4.3) calculated from the entire cohort of patients which might have been misleading or brought different conclusions.
References
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