18F-fluorodeoxyglucose positron emission tomography immediately after chemoradiotherapy predicts prognosis in patients with locoregional postoperative recurrent esophageal cancer

被引:23
作者
Jingu, Keiichi [1 ]
Kaneta, Tomohiro [2 ]
Nemoto, Kenji [3 ]
Takeda, Ken [1 ]
Ogawa, Yoshihiro [1 ]
Ariga, Hisanori [1 ]
Koto, Masashi [1 ]
Sakayauchi, Toru [1 ]
Takai, Yoshihiro [1 ]
Takahashi, Shoki [2 ]
Yamada, Shogo [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Radiat Oncol, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Sch Med, Dept Diagnost Radiol, Sendai, Miyagi 9808574, Japan
[3] Yamagata Univ, Sch Med, Dept Radiat Oncol, Yamagata 99023, Japan
关键词
FDG-PET; Recurrent esophageal cancer; Prognosis; Radiotherapy; SUVmax; SQUAMOUS-CELL CARCINOMA; RADIATION-THERAPY; F-18-FDG PET; FDG-PET; RADIOCHEMOTHERAPY; 5-FLUOROURACIL; NEDAPLATIN; DIAGNOSIS; SURVIVAL; IMPACT;
D O I
10.1007/s10147-010-0044-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objectives of this study were to reveal the utility of F-18-fluorodeoxyglucose positron emission tomography (FDG-PET) within 7 days after chemoradiotherapy to predict prognosis in patients with postoperative recurrent esophageal cancer. Patients scheduled to undergo concurrent chemoradiotherapy for postoperative locoregional recurrence of esophageal cancer were recruited. Selection criteria were: (1) locoregional recurrence, (2) no previous radiation therapy, (3) planning treatment with concurrent chemoradiotherapy, (4) FDG-PET performed < 2 weeks before chemoradiotherapy, and (5) no serious diabetes. FDG-PET was performed < 7 days after chemoradiotherapy. No more treatment after chemoradiotherapy was given until disease progression was diagnosed according to the Response Evaluation Criteria in Solid Tumors (RECIST). Correlations of FDG-PET findings with cause-specific survival and local control rates were investigated prospectively. Twenty patients were enrolled. Median observation period of patients who survived was 45.0 months. Median maximum standardized uptake value (SUVmax) after chemoradiotherapy was 2.4, and median SUVmax before chemoradiotherapy was 8.4. Cause-specific survival and local control rates were significantly better for patients with SUVmax a parts per thousand currency sign 2.4 after chemoradiotherapy (log-rank test, P = 0.033 and 0.010, respectively). SUVmax before chemoradiotherapy tended to be correlated only with cause-specific survival rate (log-rank test, P = 0.076). Change in metabolic activity of FDG was significantly correlated with local control rate (log-rank test, P = 0.042). FDG-PET performed even < 7 days after chemoradiotherapy predicts prognosis in patients with postoperative recurrent esophageal cancer.
引用
收藏
页码:184 / 190
页数:7
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