Department of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Key Laboratory of Ministry of Education of Gastrointestinal Cancer, Fujian Medical University, Fuzhou, China.
JAMA Surg. 2024 Jul 1;159(7):747-755. doi: 10.1001/jamasurg.2024.1023.
Splenic hilar lymphadenectomy has been recommended for locally advanced proximal gastric cancer (APGC) involving the greater curvature. However, it is unclear whether laparoscopic spleen-preserving splenic hilar lymphadenectomy (LSPSHL) is associated with a long-term survival benefit for APGC without greater curvature invasion.
To present the 5-year follow-up data from a randomized clinical trial that compared laparoscopic total gastrectomy (D2 group) with D2 plus LSPSHL (D2 + No. 10 group) among patients with resectable APGC.
DESIGN, SETTING, AND PARTICIPANTS: This is a post hoc secondary analysis of a randomized clinical trial that enrolled 536 patients with potentially resectable APGC (cT2-4a, N0 or N+, and M0) without greater curvature invasion from January 5, 2015, to October 10, 2018. All patients were tracked for at least 5 years. The final follow-up was on October 30, 2023.
Patients were randomly assigned in a 1:1 ratio to the D2 + No. 10 or D2 groups.
The 5-year disease-free survival (DFS) and overall survival (OS) rates were measured. Recurrence patterns and causes of death were compared.
A total of 526 patients (392 men [74.5%]; mean [SD] age, 60.6 [9.6] years) were included in the modified intent-to-treat analysis, with 263 patients in each group. The 5-year DFS rate was 63.9% (95% CI, 58.1%-69.7%) for the D2 + No. 10 group and 55.1% (95% CI, 49.1%-61.1%) for the D2 group (log-rank P = .04). A statistically significant difference was observed in the 5-year OS between the D2 + No. 10 group and the D2 group (66.2% [95% CI, 60.4%-71.9%] vs 57.4% [95% CI, 51.4%-63.4%]; log-rank P = .03). The No. 10 lymph node exhibited a therapeutic value index (TVI) of 6.5, surpassing that of Nos. 8a (TVI, 3.0), 11 (TVI, 5.8), and 12a (TVI, 0.8). A total of 86 patients in the D2 + No. 10 group (cumulative incidence, 32.7%) and 111 patients in the D2 group (cumulative incidence, 42.2%) experienced recurrence (hazard ratio, 0.72; 95% CI, 0.54-0.95; P = .02). The multivariable competing risk regression model demonstrated that D2 + No. 10 remained an independent protective factor for a lower 5-year cumulative recurrence rate after surgery (hazard ratio, 0.75; 95% CI, 0.56-1.00; P = .05). There was a significant difference in the 5-year cumulative recurrence rate at the No. 10 lymph node area between the 2 groups (D2 + No. 10 group vs D2 group: 0% vs 2.3% [n = 6]; P = .01).
This post hoc secondary analysis of a randomized clinical trial found that laparoscopic total gastrectomy with LSPSHL can improve the prognosis and reduce recurrence for APGC without greater curvature invasion. Future multicenter studies are warranted to validate these findings.
ClinicalTrials.gov Identifier: NCT02333721.
重要性:对于累及胃大弯的局部进展期近端胃癌(APGC),已推荐行脾门淋巴结清扫术。然而,对于无胃大弯侵犯的 APGC,腹腔镜保留脾脏的脾门淋巴结清扫术(LSPSHL)是否与长期生存获益相关尚不清楚。
目的:报告一项比较可切除 APGC 患者行腹腔镜全胃切除术(D2 组)与 D2 联合 LSPSHL(D2+No.10 组)的随机临床试验的 5 年随访数据。
设计、地点和参与者:这是一项随机临床试验的事后二次分析,纳入了 2015 年 1 月 5 日至 2018 年 10 月 10 日期间来自无胃大弯侵犯的潜在可切除 APGC(cT2-4a、N0 或 N+、M0)患者 536 例。所有患者至少随访 5 年。最终随访日期为 2023 年 10 月 30 日。
干预措施:患者按 1:1 比例随机分配至 D2+No.10 组或 D2 组。
主要结局和测量指标:测量 5 年无病生存率(DFS)和总生存率(OS)。比较复发模式和死因。
结果:共有 526 例患者(392 例男性[74.5%];平均[SD]年龄 60.6[9.6]岁)纳入改良意向治疗分析,每组 263 例。D2+No.10 组 5 年 DFS 率为 63.9%(95%CI,58.1%-69.7%),D2 组为 55.1%(95%CI,49.1%-61.1%)(对数秩 P=0.04)。D2+No.10 组与 D2 组的 5 年 OS 存在统计学显著差异(66.2%[95%CI,60.4%-71.9%]比 57.4%[95%CI,51.4%-63.4%];对数秩 P=0.03)。No.10 淋巴结的治疗价值指数(TVI)为 6.5,超过 No.8a(TVI,3.0)、No.11(TVI,5.8)和 No.12a(TVI,0.8)。D2+No.10 组 86 例患者(累积发病率 32.7%)和 D2 组 111 例患者(累积发病率 42.2%)发生复发(风险比,0.72;95%CI,0.54-0.95;P=0.02)。多变量竞争风险回归模型表明,D2+No.10 仍是术后较低 5 年累积复发率的独立保护因素(风险比,0.75;95%CI,0.56-1.00;P=0.05)。两组间第 10 淋巴结区域的 5 年累积复发率存在显著差异(D2+No.10 组比 D2 组:0%比 2.3%[n=6];P=0.01)。
结论:这项随机临床试验的事后二次分析发现,对于无胃大弯侵犯的 APGC,腹腔镜全胃切除术联合 LSPSHL 可改善预后并降低复发率。需要进一步的多中心研究来验证这些发现。
试验注册:ClinicalTrials.gov 标识符:NCT02333721。