Yuichiro Miki1, Masanori Tokunaga2, Keita Mori3, Norimasa Fukushima4, Kazunari Misawa5, Kazuhiro Nishikawa6, Kazumasa Fujitani7, Masaichi Ohira1, Yutaka Tanizawa8, Etsuro Bando8, Masanori Terashima9. 1. Department of Gastroenterological Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan. 2. Department of Gastrointestinal Surgery, Tokyo Medical and Dental University, Tokyo, Japan. 3. Clinical Trial Coordination Office, Shizuoka Cancer Center, Shizuoka, Japan. 4. Department of Surgery, Yamagata Prefectural Central Hospital, Yamagata, Japan. 5. Department of Gastroenterological Surgery, Aichi Cancer Center Chuo Hospital, Nagoya, Japan. 6. Department of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan. 7. Department of Surgery, Osaka General Medical Center, Osaka, Japan. 8. Division of Gastric Surgery, Shizuoka Cancer Center, Shizuoka, Japan. 9. Division of Gastric Surgery, Shizuoka Cancer Center, Shizuoka, Japan. m.terashima@scchr.jp.
Abstract
INTRODUCTION: After D2 gastrectomy for advanced gastric cancer, patients with a high drainage fluid amylase level (d-AMY) on the first postoperative day (1POD) have an especially high risk of severe abdominal infectious complications (AICs), which could be fatal. On the hypothesis that prolonged antibiotic administration could reduce the incidence of severe AICs, we conducted a randomized phase II study to evaluate the optimal treatment duration of prophylactic antibiotics for patients who underwent D2 gastrectomy and had elevated d-AMY on 1POD. METHODS: Patients whose d-AMY was >3000 IU/L on 1POD after D2 gastrectomy for gastric cancer were randomly assigned to normal prophylactic antibiotic treatment given only on the day of surgery (Group A) or to prolonged antibiotic treatment given for 1 week after surgery (Group B). The primary endpoint was the incidence of severe AICs (Clavien-Dindo grade IIIa or higher). This trial was registered as UMIN000012152. RESULTS: This study was started in December 2013 and stopped in February 2019 because of poor patient accrual. Finally, 35 and 37 patients were assigned to groups A and B, respectively. The incidences of AICs were 22.9% (eight of 35) in group A and 13.5% (five of 37) in group B. One-sided P value of the Fisher exact test was 0.234. No adverse reactions to antibiotic prophylaxis were observed in any of the patients. CONCLUSIONS: Prolonged prophylactic antibiotic administration had a marginal benefit in preventing grade III or higher AICs and caused no treatment-related morbidities.
RCT Entities:
INTRODUCTION: After D2 gastrectomy for advanced gastric cancer, patients with a high drainage fluid amylase level (d-AMY) on the first postoperative day (1POD) have an especially high risk of severe abdominal infectious complications (AICs), which could be fatal. On the hypothesis that prolonged antibiotic administration could reduce the incidence of severe AICs, we conducted a randomized phase II study to evaluate the optimal treatment duration of prophylactic antibiotics for patients who underwent D2 gastrectomy and had elevated d-AMY on 1POD. METHODS:Patients whose d-AMY was >3000 IU/L on 1POD after D2 gastrectomy for gastric cancer were randomly assigned to normal prophylactic antibiotic treatment given only on the day of surgery (Group A) or to prolonged antibiotic treatment given for 1 week after surgery (Group B). The primary endpoint was the incidence of severe AICs (Clavien-Dindo grade IIIa or higher). This trial was registered as UMIN000012152. RESULTS: This study was started in December 2013 and stopped in February 2019 because of poor patient accrual. Finally, 35 and 37 patients were assigned to groups A and B, respectively. The incidences of AICs were 22.9% (eight of 35) in group A and 13.5% (five of 37) in group B. One-sided P value of the Fisher exact test was 0.234. No adverse reactions to antibiotic prophylaxis were observed in any of the patients. CONCLUSIONS: Prolonged prophylactic antibiotic administration had a marginal benefit in preventing grade III or higher AICs and caused no treatment-related morbidities.