首页|奥沙利铂联合腹腔热灌注化疗在进展期胃癌根治术后早期应用的安全性和疗效评估

奥沙利铂联合腹腔热灌注化疗在进展期胃癌根治术后早期应用的安全性和疗效评估

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目的 以术后 1 年、3 年腹膜复发转移及围手术期并发症为主要研究终点指标,以术后 1年、3年远处转移为次要研究终点指标,探讨奥沙利铂联合腹腔热灌注化疗在局部进展期胃癌根治性手术后早期应用的安全性及临床疗效。方 法 回顾性分析江汉大学附属医院 2018年1月-2020年 1月收治的 100例局部进展期胃癌且行肿瘤根治性手术患者的临床资料,其中 55例于胃癌根治术后早期行腹腔热灌注化疗(HIPEC)治疗定义为观察组,同时收集患者热灌注化疗前后腹腔灌洗液,并行脱落细胞学检测,45例仅行胃癌根治手术治疗定义为对照组。所有患者术后均按替吉奥+奥沙利铂方案行6~8周期的全身化疗。结 果 两组胃癌患者的一般临床资料比较(性别、年龄、T分期、肿瘤部位、淋巴结转移)差异无统计学意义,资料具有可比性;两组围手术期术后严重并发症比较差异无统计学意义(P>0。05),两组术后骨髓抑制不良反应的比较差异有统计学意义(P<0。05),HIPEC治疗会增加骨髓抑制;腹腔热灌注化疗组共有 11例患者术前脱落细胞学检测到癌细胞,脱落细胞阳性率为 20%(11/55),腹腔热灌注化疗后腹腔脱落细胞学检测均未检测到癌细胞。两组术后 1 年、3 年远处复发转移比较差异无统计学意义(P>0。05),但腹腔热灌注化疗组术后 1年、3年腹膜复发转移明显小于对照组,两组比较差异有统计学意义(P<0。05)。结 论 奥沙利铂联合腹腔热灌注化疗能明显降低胃癌患者术后 1年、3年腹膜复发转移率,同时不增加围手术期术后并发症,可以作为胃癌患者的重要辅助治疗方法,改善患者的预后。
Evaluation of Safety and Efficacy of Oxaliplatin Combined with Hy-perthermic Intraperitoneal Chemotherapy in Early Application After Radical Resection of Advanced Gastric Cancer
Objective We took peritoneal recurrence and metastasis at 1 and 3 years after operation and perioperative complications as the main endpoint,and distant metastasis at 1 and 3 years after operation as the secondary endpoint,to explore the safety and clinical efficacy of oxaliplatin combined with hyperthermic intraperitoneal chemotherapy(HIPEC)in the early application after radical surgery for locally advanced gastric cancer.Methods Retrospective analysis of the clinical data of 100 patients with locally advanced gastric cancer who underwent radical surgery in Affiliated Hospital of Jianghan University,from January 2018 to January 2020.Among them,55 patients were treated with hyperthermic intraperitoneal chemotherapy at the early stage after radical surgery for gastric cancer,which was defined as the observation group.At the same time,the peritoneal lavage fluid of the patients before and after the thermal perfusion chemotherapy was collected,and exfoliative cytology was performed.45 cases who only underwent radical resection of gastric cancer were defined as the control group.All patients were treated with 6-8 cycles of systemic chemotherapy according to the tegio + oxaliplatin regimen.Results The difference in general clinical data(gender,age,T stage,tumor site,lymph node metastasis)of the two groups of gastric cancer patients was no statistically significant,and the data were comparable.There was no statistically significant difference between the two groups in postoperative serious complications during the perioperative period(P>0.05),but there was statistically significant difference in the adverse reactions of bone marrow suppression between the two groups(P<0.05).HIPEC treatment would increase bone marrow suppression.A total of 11 patients in the hyperthermic intraperitoneal chemotherapy group had cancer cells detected by exfoliative cytology before the operation,and the positive rate of exfoliative cells was 20%(11/55).No cancer cells were detected by exfoliative cytology after hyperthermic intraperitoneal chemotherapy.The difference in distant recurrence and metastasis between the two groups at 1 and 3 years after operation was not statistically significant(P>0.05),but the peritoneal recurrence and metastasis in the hyperthermic intraperitoneal chemotherapy group at 1 and 3 years after operation was significantly smaller than that in the control group,and the difference between the two groups was statistically significant(P<0.05).Conclusion Oxaliplatin combined with hyperthermic intraperitoneal chemotherapy can significantly reduce the rate of peritoneal recurrence and metastasis in patients with gastric cancer at 1 and 3 years after operation without increasing postoperative complications in the perioperative period.It can be used as an important adjuvant treatment for patients with gastric cancer and improve the prognosis of patients.

gastric cancerhyperthermic intraperitoneal chemotherapyoxaliplatinabdominal detachment of cancer cells

蔡高平、余阳

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江汉大学 医学部,湖北 武汉 430056

江汉大学 附属医院胃肠外科,湖北 武汉 430015

胃癌 腹腔热灌注化疗 奥沙利铂 腹腔脱落癌细胞

2024

江汉大学学报(自然科学版)
江汉大学

江汉大学学报(自然科学版)

影响因子:0.413
ISSN:1673-0143
年,卷(期):2024.52(1)
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