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J Thorac Cardiovasc Surg 2008;136:205-212
© 2008 The American Association for Thoracic Surgery


General Thoracic Surgery

Lack of fludeoxyglucose F 18 uptake in posttreatment positron emission tomography as a significant predictor of survival after subsequent surgery in multimodality treatment for patients with locally advanced esophageal squamous cell carcinoma

Ichirou Higuchi, MDa, Takushi Yasuda, MDa,*, Masahiko Yano, MDa, Yuichirou Doki, MDa, Hiroshi Miyata, MDa, Mitsuaki Tatsumi, MDb, Hironori Fukunaga, MDa, Shuji Takiguchi, MDa, Yoshiyuki Fujiwara, MDa, Jun Hatazawa, MDb, Morito Monden, MDa

a Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan
b Department of Nuclear Medicine and Tracer Kinetics, Graduate School of Medicine, Osaka University, Osaka, Japan

Received for publication June 19, 2007; revisions received January 25, 2008; accepted for publication February 15, 2008.

* Address for reprints: Takushi Yasuda, MD, Department of Surgery, School of Medicine, Kinki University, 377-2, Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan. (Email: tyasuda{at}surg.med.kindai.ac.jp).

Objective: Patients with advanced esophageal squamous cell carcinoma receive neoadjuvant chemotherapy or chemoradiotherapy to improve survival, but benefits are observed only in those with histologic response. Positron emission tomography with fludeoxyglucose F 18 (INN fludeoxyglucose [18F]) detects accumulation of glucose analog in viable cancer cells. This study investigated the usefulness of positron emission tomography with fludeoxyglucose F 18 in assessment of response of advanced esophageal squamous cell carcinoma to neoadjuvant treatment to establish new criteria to predict postoperative long-term survival.

Methods: Fifty patients with locally advanced esophageal squamous cell carcinoma who received neoadjuvant therapy (chemotherapy 35, chemoradiotherapy 15) underwent positron emission tomography with fludeoxyglucose F 18 before surgical resection in evaluation of posttreatment maximum standardized uptake value, residual tumor size (maximum square area of longitudinal axis), histologic response, and postoperative survival.

Results: After treatment, uptake was not noted in 21 patients (posttreatment maximum standardized uptake value <2.5, negative) but was detected in 29 (≥2.5, positive). Residual tumor size ranged from 0 to 54.0 mm2 for negative results and 55.0 to 676.0 mm2 for positive, clearly distinguishing histologic major response from nonresponse. The negative group demonstrated significantly higher 5-year cause-specific survival (67.7%) and lower hematogenous recurrence (4.8%) than the 36.5% and 37.0% values in the positive group, (P < .0042 and P = .0083, respectively). Univariate Cox regression analyses identified posttreatment maximum standardized uptake value (cutoff 2.5) as the only preoperative prognostic factor (P = .0071).

Conclusion: Posttreatment positron emission tomography with fludeoxyglucose F 18 reliably predicted histologic response and postoperative survival in advanced esophageal squamous cell carcinoma. This tool could potentially be used to tailor optimal treatment according to individual responses.



Abbreviations and Acronyms FDG = fludeoxyglucose F 18; PET = positron emission tomography; SCC = squamous cell carcinoma; SUVmax = maximum standardized uptake value








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