氟尿嘧啶联合紫杉醇、奥沙利铂治疗晚期胃印戒细胞癌的疗效观察。

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Mi Liu, Bei Feng, Na He, Rong Yan, Jie Qin
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引用次数: 0

摘要

背景:胃印戒细胞癌(GSRC)是一种独特的胃癌类型。它是一种粘液分泌腺癌,早期可发展为远处转移。由于分化差、侵袭性强、进展快等高危特点,应优先进行早期手术干预。目的:探讨氟尿嘧啶(5-FU)联合紫杉醇、奥沙利铂治疗晚期GSRC的临床疗效。方法:选择2020年1月至2021年6月期间共85例晚期GSRC患者,随机分为对照组(n = 42,接受标准化疗)和治疗组(n = 43,接受奥沙利铂、5-FU和紫杉醇单药治疗)。治疗组患者给予紫杉醇135 mg/m2输注3小时,叶酸钙400 mg/m2输注(或左叶酸钙200 mg/m2) 2小时,奥沙利铂85 mg/m2输注2小时。随后使用便携式泵连续静脉滴注2200-2400 mg/m2 5-FU 46小时。结果:治疗组患者中位生存时间为11.7个月,客观缓解率(ORR)为32.5%,显著高于对照组(P < 0.05)。血清癌胚抗原(CEA)、碳水化合物抗原19-9 (CA19-9)、白蛋白水平与晚期GSRC治疗效果相关(P < 0.01),而血清总蛋白与晚期GSRC治疗效果无相关性(P < 0.05)。对所有患者进行安全性和生存率评估。66例患者进行了短期疗效评估,疾病控制率为89.4%,ORR为48.5%。中位无进展生存期为7.0个月(95%可信区间[CI]: 6.85-7.15),中位总生存期为10.6个月(95%CI: 9.86-11.3)。初级III/IV级不良事件包括中性粒细胞减少(22.1%)和周围神经毒性(10.3%)。结论:该治疗方案对晚期GSRC患者更有效。血清CEA、CA19-9和白蛋白水平预测化疗疗效,而总蛋白浓度相关性最小且不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of fluorouracil combined with paclitaxel and oxaliplatin for the treatment of advanced gastric signet ring cell carcinoma.

Background: Gastric signet ring cell carcinoma (GSRC) is a distinctive type of gastric cancer. It is a mucus-secreting adenocarcinoma that may progress to distant metastasis at an early stage. Because of poor differentiation, aggressive invasion, rapid progression, and other high-risk characteristics, early surgical intervention should be prioritized.

Aim: To explore the clinical efficacy of fluorouracil (5-FU) combined with paclitaxel and oxaliplatin for the treatment of advanced GSRC.

Methods: A total of 85 patients with advanced GSRC were selected between January 2020 and June 2021 and randomly divided into a control group (n = 42, receiving standard chemotherapy) and a treatment group (n = 43, receiving monotherapy with oxaliplatin, 5-FU, and paclitaxel). Patients in the treatment group received a 135 mg/m2 infusion of paclitaxel for 3 hours, a 400 mg/m2 infusion of calcium folate (or 200 mg/m2 of levocalcium folate) for 2 hours, and an 85 mg/m2 infusion of oxaliplatin for 2 hours. This was followed by a continuous intravenous infusion of 2200-2400 mg/m2 5-FU for 46 hours using a portable pump.

Results: The treatment group showed a median survival time of 11.7 months and an objective response rate (ORR) of 32.5%, significantly higher than the control group (P < 0.05). Serum carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), and albumin levels were correlated with treatment effectiveness in advanced GSRC (P < 0.01), but total serum protein was not correlated (P > 0.05). Safety and survival were assessed in all patients. Short-term efficacy was evaluated in 66 patients, with a disease control rate of 89.4% and an ORR of 48.5%. Median progression-free survival was 7.0 months (95% confidence interval [CI]: 6.85-7.15), and median overall survival was 10.6 months (95%CI: 9.86-11.3). Primary grade III/IV adverse events included neutropenia (22.1%) and peripheral neurotoxicity (10.3%).

Conclusion: This treatment regimen is more effective for patients with advanced GSRC. Serum levels of CEA, CA19-9, and albumin predicted chemotherapy efficacy, while total protein concentration correlated minimally and insignificantly.

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