Department of Internal Medicine, College of Medicine, Hanyang University, Seoul, Korea.
Cancer Res Treat. 2004 Jun;36(3):182-6. doi: 10.4143/crt.2004.36.3.182. Epub 2004 Jun 30.
To evaluate the efficacy and toxicity of heptaplatin, paclitaxel, and 5-fluorouracil combination chemotherapy in patients with advanced gastric cancer.
Between July 2002 and September 2003, nineteen patients were enrolled in this study. Paclitaxel 135 mg/m(2) iv on day 1, heptaplatin 400 mg/m(2) iv on day 2 and 5-fluorouracil 800 mg/m(2) on day 2 approximately 4 were administered and the regimen was repeated every 3 weeks.
The median age of the patients was 60 years (range: 32 approximately 74) and the most common sites of metastasis were liver and lymph nodes. In the 16 evaluated patients, the overall response rate was 43.8%, but this was without any complete response. The median time to disease progression was 3.93 months (range: 0.26 approximately 8.1) and the median response duration for the 7 responding patients was 3.83 months (range: 1.48 approximately 6.07). The median overall survival for 19 patients was 7.01 months (range: 0.26 approximately 17.44). A median of 3 cycles (range: 1 approximately 7) and a total of 65 cycles were administered and evaluated for toxicity. The most common hematologic toxicities were NCI grade I/II anemia (47.7%), neutropenia (9.2%) and thrombocytopenia (6.2%). The most common non-hematologic toxicities more than grade II were nausea/vomiting (30.8%/9.2%). One elderly patient with ECOG 2 had a life-threatening complication of pneumonia.
The combination of heptaplatin, paclitaxel, and 5-fluorouracil showed significant activity and favorable toxicity profiles in patients with advanced gastric cancer. However, one elderly patient who had poor performance experienced a life-threatening toxicity/complication. Our results suggest that the efficacy of this combination chemotherapy can be maximized when administered to the patients with good performance status. Further studies with large numbers of patients and long-term follow-up study will be needed.
评估奥沙利铂、紫杉醇和氟尿嘧啶联合化疗治疗晚期胃癌的疗效和毒性。
2002 年 7 月至 2003 年 9 月,共纳入 19 例患者。紫杉醇 135mg/m²,静脉滴注,第 1 天;顺铂 400mg/m²,静脉滴注,第 2 天;氟尿嘧啶 800mg/m²,静脉滴注,第 2 天,每 3 周重复一次。
患者的中位年龄为 60 岁(范围:32-74 岁),最常见的转移部位是肝脏和淋巴结。在 16 例可评估的患者中,总缓解率为 43.8%,但没有完全缓解。疾病进展的中位时间为 3.93 个月(范围:0.26-8.1),7 例缓解患者的中位缓解持续时间为 3.83 个月(范围:1.48-6.07)。19 例患者的中位总生存期为 7.01 个月(范围:0.26-17.44)。中位 3 个周期(范围:1-7 个),共 65 个周期用于评估毒性。最常见的血液学毒性为 NCI 分级 I/II 级贫血(47.7%)、中性粒细胞减少症(9.2%)和血小板减少症(6.2%)。高于 II 级的最常见非血液学毒性为恶心/呕吐(30.8%/9.2%)。1 例 ECOG 评分为 2 的老年患者发生了危及生命的肺炎并发症。
奥沙利铂、紫杉醇和氟尿嘧啶联合方案治疗晚期胃癌具有显著的疗效和良好的毒性特征。然而,1 例体力状态差的老年患者发生了危及生命的毒性/并发症。我们的结果表明,当给予体力状态良好的患者时,这种联合化疗的疗效可以最大化。需要进一步进行更大规模的患者和长期随访研究。