Eguchi Teruo, Fujii Masashi, Wakabayashi Kazuhiko, Aisaki Kazuo, Tsuneda Yutaka, Kochi Mitsugu, Takayama Tadatoshi
Third Department of Surgery, Nihon University School of Medicine, 30-1 Oyaguchikami machi, Itabashi-ku, Tokyo 173-8610, Japan.
Hepatogastroenterology. 2003 Sep-Oct;50(53):1735-8.
BACKGROUND/AIMS: There are few reports on chemotherapy for poor prognosis terminal patients with peritoneal dissemination of gastric cancer, especially in those with renal dysfunction, because of the possibility of severe toxicity. We conducted a study of the combination of docetaxel and 5-fluorouracil for the treatment of these patients to improve quality of life because of its low toxicity.
Five patients were treated in this study. All patients had a large volume of carcinomatous fluid in the abdomen, without liver or distant metastasis. The respective doses of docetaxel and 5-fluorouracil were 60 mg/m2 on day 1 and 370 mg/m2 on days 1 to 5 by intravenous infusion. Patients received this treatment 2-7 times every 2-3 weeks.
Grade III/IV toxicity occurred, consisting of neutropenia (100%) and diarrhea (40%). No patients developed renal dysfunction. Carcinomatous fluid volume diminished for 15-96 days. Quality of life questionnaire score and performance status scale was significantly improved from 75-86 to 51-61 (p = 0.041) and 3-4 to 0-1 (p = 0.039), respectively. All patients were able to leave hospital after this treatment. Four of five patients died and median survival time was 223 days. Two of five patients achieved partial response and three patients showed no response (response rate 40%).
This new combination therapy had benefit for terminal patients with peritoneal dissemination of gastric cancer.
背景/目的:关于预后较差的晚期胃癌腹膜播散患者的化疗报道较少,尤其是肾功能不全的患者,因为可能会出现严重毒性。我们开展了一项多西他赛与5-氟尿嘧啶联合治疗这些患者的研究,因其毒性低,有望改善生活质量。
本研究纳入5例患者。所有患者腹腔内均有大量癌性积液,无肝转移或远处转移。多西他赛和5-氟尿嘧啶的各自剂量分别为第1天静脉输注60mg/m²和第1至5天静脉输注370mg/m²。患者每2 - 3周接受2 - 7次该治疗。
出现了III/IV级毒性反应,包括中性粒细胞减少(100%)和腹泻(40%)。无患者出现肾功能不全。癌性积液量在15 - 96天内减少。生活质量问卷评分和体能状态量表评分分别从75 - 86显著提高至51 - 61(p = 0.041)和从3 - 4显著提高至0 - 1(p = 0.039)。所有患者经此治疗后均能出院。5例患者中有4例死亡,中位生存时间为223天。5例患者中有2例达到部分缓解,3例患者无反应(缓解率40%)。
这种新的联合疗法对晚期胃癌腹膜播散患者有益。