Huisman C, Giaccone G, van Groeningen C J, Sutedja G, Postmus P E, Smit E F
Department of Pulmonary Diseases, University Hospital Vrije Universiteit, Amsterdam, The Netherlands.
Lung Cancer. 2001 Aug-Sep;33(2-3):267-75. doi: 10.1016/s0169-5002(01)00187-8.
Many regimens of gemcitabine-cisplatin chemotherapy have proven activity in patients with advanced non-small cell lung cancer (NSCLC). However, the optimal dose and schedule still have to be established.
We conducted a phase II study with administration of cisplatin 50 mg/m(2) on days 1 and 8 and gemcitabine 800 mg/m(2) on days 2, 9 and 15. This schedule was selected to optimise the synergism between the two drugs and reduce toxicity due to high dose cisplatin.
Thirty-six chemo-naive patients with stage IIIA, IIIB or IV NSCLC entered the study (26 men, 10 women; median age 58 years, range 29-74). Twenty patients achieved a partial response: 7 out of 10 stage IIIA patients, 7 out of 13 stage IIIB patients and 6 out of 13 stage IV patients. On intent-to-treat basis, the overall response rate (RR) was 58% (95% confidence interval, 42-74%). Ninety percent of stage IIIA patients and 46% of stage IIIB patients received adjuvant surgery or radiotherapy. Overall median duration of response was 28 weeks (range 6-147 weeks). For stage IIIA, IIIB and IV patients, these numbers were 91, 13 and 23 weeks, respectively. One-year survival was 49% with 90%, 23% and 42% for stage IIIA, IIIB and IV patients, respectively. The main toxicity was myelosuppression. WHO grades 3 and 4 leukopenia occurred in 67% of patients, whereas 61% experienced grade 3 or 4 thrombocytopenia. Although hematological toxicity was clinically tolerable, it frequently led to omission of gemcitabine administration on day 15. The incidence of non-hematological toxicity was very low.
This regimen of cisplatin on days 1 and 8 and gemcitabine on days 2, 9 and 15 induced a high RR in patients with advanced NCSLC. Frequent omission of gemcitabine day 15 is a limitation of this schedule. This should be an important factor in a practical approach to decide on the most optimal schedule of the cisplatin plus gemcitabine combination.
许多吉西他滨 - 顺铂化疗方案已被证明对晚期非小细胞肺癌(NSCLC)患者有活性。然而,最佳剂量和给药方案仍有待确定。
我们进行了一项II期研究,在第1天和第8天给予顺铂50mg/m²,在第2天、第9天和第15天给予吉西他滨800mg/m²。选择该给药方案是为了优化两种药物之间的协同作用,并降低高剂量顺铂所致的毒性。
36例初治的IIIA期、IIIB期或IV期NSCLC患者进入研究(26例男性,10例女性;中位年龄58岁,范围29 - 74岁)。20例患者达到部分缓解:10例IIIA期患者中的7例,13例IIIB期患者中的7例,13例IV期患者中的6例。在意向性分析的基础上,总缓解率(RR)为58%(95%置信区间,42 - 74%)。90%的IIIA期患者和46%的IIIB期患者接受了辅助手术或放疗。总体中位缓解持续时间为28周(范围6 - 147周)。对于IIIA期、IIIB期和IV期患者,这些数字分别为91周、13周和23周。1年生存率为49%,IIIA期、IIIB期和IV期患者分别为90%、23%和42%。主要毒性为骨髓抑制。67%的患者发生WHO 3级和4级白细胞减少,而61%的患者经历3级或4级血小板减少。尽管血液学毒性在临床上可耐受,但它经常导致第15天吉西他滨给药的遗漏。非血液学毒性的发生率非常低。
这种在第1天和第8天给予顺铂、在第2天、第9天和第15天给予吉西他滨的方案在晚期NCSLC患者中诱导了高RR。第15天经常遗漏吉西他滨给药是该给药方案的一个局限性。这应该是在实际应用中决定顺铂加吉西他滨联合方案最优化给药方案时的一个重要因素。