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从临床肿瘤学家角度看4型胃癌的治疗策略

[Therapeutic strategy for type 4 gastric cancer from the clinical oncologist standpoint].

作者信息

Sasaki Tohru, Koizumi Wasaburo, Higuchi Katsuhiko, Ishido Kenji, Ae Takako, Nakatani Kento, Katada Chikatoshi, Tanabe Satoshi, Saigenji Katsunori

机构信息

Dept. of Gastroenterology, Kitasato University East Hospital.

出版信息

Gan To Kagaku Ryoho. 2007 Jul;34(7):988-92.

Abstract

Type 4 gastric cancer has a poor prognosis compared with other types of advanced gastric cancer because of the high incidence of peritoneal metastasis which causes intestinal obstruction, hydronephrosis, or obstructive jaundice. Surgical treatment is often only palliative, and systematic chemotherapy is considered to be important for long survival. S-1 showed a higher response rate for undifferentiated-type adenocarcinoma, and S-1 alone or its combination regimens demonstrated greater anti-tumor effects and longer survival time for gastric linitis plastica compared with conventional 5-FU regimens in our historical control study (response rate: S-1/non S-1 57.9%/27.9%, p<0.01; MST: S-1/non S-1 402 days/213 days, p<0.01). S-1 regimens may also improve the survival in patients with type 4 gastric cancer in neoadjuvant or adjuvant settings, but further prospective studies are warranted to prove its significance. Paclitaxel also has a high response rate for undifferentiated-type adenocarcinoma, and can be expected to show high efficacy for peritoneal dissemination. Irinotecan should not be administered in case of intestinal obstruction because its toxicity may be increased. However,survival of patients with type 4 gastric cancer may improve with the availability of active agents like S-1, taxanes, irinotecan as reported in colorectal cancer. Therefore,irinotecan should be administered carefully before intestinal obstruction occurs.

摘要

与其他类型的进展期胃癌相比,4型胃癌预后较差,因为腹膜转移发生率高,可导致肠梗阻、肾积水或梗阻性黄疸。手术治疗往往仅为姑息性,全身化疗被认为对延长生存期很重要。S-1对未分化型腺癌显示出更高的缓解率,在我们的历史对照研究中,与传统的5-氟尿嘧啶方案相比,单独使用S-1或其联合方案对皮革胃显示出更大的抗肿瘤作用和更长的生存期(缓解率:S-1/非S-1 57.9%/27.9%,p<0.01;中位生存期:S-1/非S-1 402天/213天,p<0.01)。S-1方案在新辅助或辅助治疗中也可能改善4型胃癌患者的生存期,但需要进一步的前瞻性研究来证明其意义。紫杉醇对未分化型腺癌也有较高的缓解率,有望对腹膜播散显示出高效。如果发生肠梗阻则不应给予伊立替康,因为其毒性可能会增加。然而,如在结直肠癌中报道的那样,像S-1、紫杉烷、伊立替康等活性药物的应用可能会改善4型胃癌患者的生存期。因此,应在肠梗阻发生前谨慎给予伊立替康。

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