Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi, Japan.
Department of Biostatistics, School of Medicine, Yokohama City University, Kanagawa, Japan.
J Gynecol Oncol. 2024 Jul;35(4):e37. doi: 10.3802/jgo.2024.35.e37. Epub 2024 Jan 1.
In Japan, perioperative prophylaxis of pulmonary embolism (PE) in gynecologic cancer patients with preoperative asymptomatic venous thromboembolism (VTE) has not been well established yet. The GOTIC-VTE trial was a prospective, multi-center, single-arm clinical trial to investigate the prevention of postoperative symptomatic PE onset by seamless anticoagulant therapy from the preoperative period to 4 weeks after surgery instead of using intermittent pneumatic compression.
Anticoagulant therapy was started immediately after asymptomatic VTE diagnosis and stopped preoperatively according to the rules of each institution. Unfractionated heparin administration was resumed within 12 hours postoperatively, and this was followed by the switch to low-molecular-weight heparin and subsequently, edoxaban; this cycle was continued for 28 days. Primary outcome was the occurrence of symptomatic PE in 28 days postoperatively. Secondary outcomes were the incidence of VTE-related events in 28 days and 6 months postoperatively and protocol-related adverse events.
Between February 2018 and September 2020, 99 patients were enrolled; of these, 82 patients were assessed as the full analysis set, including 58 for ovarian cancer, fallopian tube, or peritoneal cancer; 21 for endometrial cancer; and 3 for cervical cancer. No symptomatic PE was observed within 28 days postoperatively; two patients had bleeding events (major bleeding and clinically relevant nonmajor bleeding) and three had grade 3 adverse events (increased alanine transaminase, aspartate aminotransferase, or gamma-glutamyl transferase).
The multifaceted perioperative management for gynecologic malignancies with asymptomatic VTE effectively prevented postoperative symptomatic PE.
JRCT Identifier: jRCTs031180124.
在日本,对于术前无症状静脉血栓栓塞症(VTE)的妇科癌症患者,其围手术期肺栓塞(PE)预防措施尚未得到充分确立。GOTIC-VTE 试验是一项前瞻性、多中心、单臂临床试验,旨在通过从术前到术后 4 周不间断抗凝治疗,而非使用间歇充气压迫来预防术后有症状的 PE 发作。
在诊断出无症状 VTE 后立即开始抗凝治疗,并根据各机构的规定在术前停药。术后 12 小时内恢复普通肝素给药,随后转为低分子肝素,再转为依度沙班;此周期持续 28 天。主要结局为术后 28 天内发生有症状的 PE。次要结局为术后 28 天和 6 个月时的 VTE 相关事件发生率以及与方案相关的不良事件。
2018 年 2 月至 2020 年 9 月,共纳入 99 例患者;其中 82 例患者被评估为全分析集,包括卵巢癌、输卵管或腹膜癌 58 例,子宫内膜癌 21 例,宫颈癌 3 例。术后 28 天内未观察到有症状的 PE;2 例患者发生出血事件(主要出血和临床相关非重大出血),3 例患者发生 3 级不良事件(丙氨酸氨基转移酶、天冬氨酸氨基转移酶或γ-谷氨酰转移酶升高)。
针对无症状 VTE 的妇科恶性肿瘤的多方面围手术期管理可有效预防术后有症状的 PE。
日本临床试验注册编号:jRCTs031180124。