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Comparative Study of Gemcitabine Plus Cisplatin and Gemcitabine Plus Fluorouracil in the Treatment of Advanced Pancreatic Cancer

机译:吉西他滨联合顺铂与吉西他滨联合氟尿嘧啶治疗晚期胰腺癌的对比研究

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OBJECTIVE To compare the efficacy and toxicity of gemcitabine plus cis-platin and gemcitabine plus fluorouracil in the treatment of advanced pancreatic cancer. METHODS Sixty patients with advanced pancreatic cancer were randomly divided into a GP group (gemcitabine + cisplatin, 30 cases) and a GF group (gemcitabine + fluorouracil, 30 cases). All patients were treated with gemcitabine at a dose of 1.000mg/m~2 (diluted in 100ml saline solution over 30 min) once a week for 3 consecutive weeks. The GP Group was followed by 40mg cisplatin via intravenous drip on days 15,16,17. Group GF was followed by 500mg/m~2 5-Fu (diluted in 5% glucose-saline (GS) 500ml, intravenously, over 6 hr) every day for five subsequent days. RESULTS In the GP group, eight cases (32.0%) were PR and MR, the median survival time was 8.7 months, the Clinical Beneficial Rate (CBR) was 57.7%, and the CA19-9 decreased by over 50% in 13cases (48.1%). In the GF group, 11 cases (45.8%) were PR and MR, the survival time was 10.1 months, the CBR was 82.1%, and CA19-9 decreased by over 50% in 15 cases(53.6%). There was a significant difference in the CBR between the two groups (P<0.05). The main toxicities in both groups were leucopenia and thrombocytopenia with no significant difference. CONCLUSIONS The treatment given to either the GP or GF group is a feasible and well -tolerated chemotherapy regimen for treating advanced pancreatic cancer with improved therapeutic efficacy and few side effects. The median survival period is long and the CBR is high, especially with the GF regimen.
机译:目的比较吉西他滨联合顺铂和吉西他滨联合氟尿嘧啶治疗晚期胰腺癌的疗效和毒性。方法将60例晚期胰腺癌患者随机分为GP组(吉西他滨+顺铂30例)和GF组(吉西他滨+氟尿嘧啶30例)。所有患者均连续3周每周以1.000mg / m〜2的剂量(在30分钟内用100ml盐溶液稀释)接受吉西他滨治疗。 GP组之后在第15、16、17天通过静脉滴注40mg顺铂。 GF组随后每天连续五天每天服用500mg / m〜2 5-Fu(用5%葡萄糖盐水(GS)500ml稀释,经6小时静脉注射)。结果GP组中PR和MR占8例(32.0%),中位生存期8.7个月,临床受益率(CBR)为57.7%,CA19-9下降13%(48.1)。 %)。 GF组PR和MR的11例(45.8%),生存时间为10.1个月,CBR为82.1%,CA19-9下降了50%以上(15.6%)。两组之间的CBR有显着差异(P <0.05)。两组的主要毒性为白细胞减少症和血小板减少症,无显着差异。结论GP或GF组的治疗都是可行且耐受性良好的化疗方案,可用于治疗晚期胰腺癌,且具有更高的治疗效果,且副作用很少。中位生存期长且CBR高,尤其是GF方案。

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