[18F]fluorodeoxyglucose uptake by positron emission tomography predicts outcome of non-small-cell lung cancer

Ryohei Sasaki, Ritsuko Komaki, Homer Macapinlac, Jeremy Erasmus, Pamela Allen, Kenneth Forster, Joe B. Putnam, Roy S. Herbst, Cesar A. Moran, Donald A. Podoloff, Jack A. Roth, James D. Cox

Research output: Contribution to journalArticlepeer-review

270 Scopus citations

Abstract

Purpose: To determine whether the standardized uptake value (SUV) of [ 18F]fluorodeoxyglucose uptake by positron emission tomography could be a prognostic factor for non-small-cell lung cancer (NSCLC). Patients and Methods: One hundred sixty-two patients with stage I to IIIb NSCLC were analyzed. Overall survival (OS), disease-free survival (DFS), distant metastasis-free survival (DMFS), and local-regional control (LRC) were calculated by the Kaplan-Meier method and evaluated with the log-rank test. The prognostic significance was assessed by univariate and multivariate analyses. Results: There were 93 patients treated with surgery and 69 patients treated with radiotherapy. A cutoff of 5 for the SUV for the primary tumor showed the best discriminative value. The SUV for the primary tumor was a significant predictor of OS (P = .02) in both groups. Low SUVs (< 5.0) showed significantly better DFS rates than those with high SUVs (> 5.0; surgery group, P = .02; radiotherapy group, P = .0005). Low SUVs (≤ 5.0) indicated a significantly better DFS than those with high SUVs (> 5.0; stage I or II, P = .02; stage IIIa or IIIb, P = .004). However, using the same cutoff point of 5, the SUV for regional lymph nodes was not a significant indicator for DFS (P = .19), LRC (P = .97), or DMFS (P = .17). The multivariate analysis showed that the SUV for the primary tumor was a significant prognostic factor for OS (P = .03) and DFS (P = .001). Conclusion: The SUV of the primary tumor was the strongest prognostic factor among the patients treated by curative surgery or radiotherapy.

Original languageEnglish (US)
Pages (from-to)1136-1143
Number of pages8
JournalJournal of Clinical Oncology
Volume23
Issue number6
DOIs
StatePublished - Feb 20 2005

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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