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腹腔内注射紫杉醇治疗结直肠癌伴腹膜转移的疗效。

Efficacy of intraperitoneally administered paclitaxel for colorectal cancer with peritoneal metastases.

机构信息

Division of Surgical Oncology, Department of Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.

Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Aichi, 464-0021, Japan.

出版信息

Int J Colorectal Dis. 2020 Oct;35(10):1945-1949. doi: 10.1007/s00384-020-03649-0. Epub 2020 Jun 3.

Abstract

PURPOSE

Prognosis after peritoneal metastases in colorectal cancer is worse than that after lung or liver metastases. Previously, we demonstrated the safety of intraperitoneal (ip) administration of paclitaxel (PTX) combined with mFOLFOX6/CapeOX plus bevacizumab for colorectal cancer with peritoneal metastasis in a phase-I trial. Here, we evaluated the efficacy of this chemotherapy.

METHODS

We enrolled six patients with histologically confirmed peritoneal metastases secondary to colorectal cancer. PTX was administered through a peritoneal access port, in combination with oxaliplatin-based systematic chemotherapy. Response rate, progression-free survival, 1-year survival rate, frequency of improvement in peritoneal cancer index (PCI), and cytology in peritoneal lavage were evaluated. This study was registered in the University Hospital Medical Information Network Clinical Trial Registry on July 1, 2016 (UNIN000022924).

RESULTS

Three patients received the mFOLFOX6-bevacizumab regimen, whereas the other three received the CapeOX-bevacizumab regimen. The response rate was 25%. PCI score improved in 50% of the cases. Peritoneal lavage cytology that was positive in five patients before initiating the chemotherapy turned negative during chemotherapy in all patients. One-year survival rate was 100%, progression-free survival was 8.8 months (range, 6.8-12 months), and median survival time was 29.3 months.

CONCLUSION

The ip administration of PTX with systemic chemotherapy can potentially control peritoneal metastases in colorectal cancer.

摘要

目的

结直肠癌腹膜转移的预后比肺或肝转移差。此前,我们在一项 I 期试验中证明了腹腔内(ip)给予紫杉醇(PTX)联合 mFOLFOX6/CapeOX 加贝伐单抗治疗结直肠癌伴腹膜转移的安全性。在此,我们评估了这种化疗的疗效。

方法

我们招募了 6 名经组织学证实的结直肠癌继发腹膜转移的患者。PTX 通过腹膜进入端口给药,与奥沙利铂为基础的系统化疗联合使用。评估了反应率、无进展生存期、1 年生存率、腹膜癌指数(PCI)改善频率和腹膜灌洗细胞学。本研究于 2016 年 7 月 1 日在大学医院医疗信息网临床试验注册中心注册(UNIN000022924)。

结果

3 名患者接受 mFOLFOX6-贝伐单抗方案,另 3 名患者接受 CapeOX-贝伐单抗方案。反应率为 25%。50%的病例 PCI 评分得到改善。在开始化疗前,5 名患者的腹膜灌洗细胞学为阳性,所有患者在化疗期间均转为阴性。1 年生存率为 100%,无进展生存期为 8.8 个月(6.8-12 个月),中位生存时间为 29.3 个月。

结论

系统化疗联合腹腔内 PTX 给药可能有助于控制结直肠癌的腹膜转移。

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