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Prospective Multicenter Feasibility Study of Laparoscopic Sentinel Basin Dissection for Organ Preserving Surgery in Gastric Cancer

机译:腹腔镜前哨盆腔清扫术在胃癌器官保存手术中的前瞻性多中心可行性研究

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摘要

The clinical application of sentinel node biopsies in early gastric cancer is still controversial even though it appears promising. This study was conducted as a prerequisite quality control for surgical standardization of laparoscopic sentinel basin dissection (SBD) prior to the initiation of a phase III trial.Laparoscopic SBD was performed in patients with preoperative stage T1-2N0 and tumor size <4 cm in diameter. Intraoperative endoscopic submucosal injection of a standardized dual tracer was administered. All retrieved sentinel basin nodes (SBN) were investigated with intraoperative frozen hematoxylin and eosin (H&E) staining. A strict checklist consisting of 7 essential steps was followed during laparoscopic SBD as the quality control study for a phase III trial. Completion of all essential steps in the checklist for 10 cases was used to define a qualified institution.Seven institutions participated and 112 patients were enrolled in this study. However, 4 patients were excluded owing to screening failure. The mean number of cases required for institutional qualification was 15 cases (range, 13–20 cases). Sentinel basins (SB) were detected and dissected in 100 of the 108 patients (92.6%); the median number of SB and SBN was 2 and 7, respectively. Lymph node metastases were detected in 10 patients by postoperative permanent H&E staining and they were detected by SBD in all 10 patients. Frozen results of SBN were compatible with permanent staining reports.Laparoscopic SBD is feasible and demonstrated improved sensitivity in detecting metastatic lymph nodes compared to the previous study. A future phase III randomized trial comparing laparoscopic SBD with organ-preserving gastrectomy and laparoscopic standard gastrectomy seems promising for qualified institutions.
机译:尽管前哨淋巴结活检在早期胃癌中的临床应用仍存在争议。这项研究是进行III期临床试验之前进行腹腔镜前哨纵隔盆地剥离术(SBD)手术标准化的必要质量控制。术前T1-2N0且肿瘤直径<4 cm的患者进行了腹腔镜SBD 。术中内镜下粘膜下注射标准化的双重示踪剂。所有术前冰冻苏木和曙红(H&E)染色调查了所有取下的前哨盆地结节(SBN)。腹腔镜SBD期间遵循严格的清单,包括7个基本步骤,作为III期临床试验的质量控制研究。通过检查清单中10例患者的所有基本步骤的完成来定义合格的机构。该机构参加了7家机构的112名患者。然而,由于筛查失败,有4名患者被排除在外。获得机构资格所需的平均病例数为15例(范围13–20例)。在108名患者中有100名(92.6%)发现并解剖了前哨盆(SB)。 SB和SBN的中位数分别为2和7。术后永久H&E染色检测10例患者的淋巴结转移,所有10例患者均通过SBD检测。 SBN的冷冻结果与永久性染色报告相符。与以前的研究相比,腹腔镜SBD是可行的,并证明了在检测转移性淋巴结方面的灵敏度更高。一项将腹腔镜SBD与保留器官的胃切除术和腹腔镜标准胃切除术进行比较的未来III期随机试验对于合格的机构来说似乎很有希望。

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