Groen H J, van der Leest A H, de Vries E G, Uges D R, Szabó B G, Mulder N H
Department of Pulmonary Diseases, University Hospital Groningen, The Netherlands.
Br J Cancer. 1995 Oct;72(4):992-7. doi: 10.1038/bjc.1995.448.
A phase I study was performed in 21 patients with previously untreated, locally inoperable, non-small-cell lung cancer (NSCLC) with ambulatory continuous carboplatin infusion together with continuous thoracic irradiation over 6 weeks. A dose range for carboplatin of 15 mg m-2 day-1 during the last 21 days (first level), during the last 31 days (second level), or during 6 weeks of the radiation period (third level) and thereafter 20 or 25 mg m-2 day-1 during 6 weeks of radiation (fourth and fifth level) was used. The total radiation dose was 60 Gy given as 2 Gy day-1 for 5 days week-1. The first three patients received radiotherapy without carboplatin. WHO grade III/IV leucopenia and thrombocytopenia occurred in the last two dose levels in two out of six and one out of six patients with 20 mg m-2 day-1 respectively, and in all three patients with 25 mg m-2 day-1 (dose-limiting toxicity). One local infection around the port and a subclavian vein thrombosis occurred. Radiation toxicity of the lung and oesophagus did not seem to be influenced by carboplatin treatment. Out of 21 patients one had a complete response (CR), ten partial response (PR), six stable disease (SD) and four progressive disease (PD). Total (TPt) and ultrafilterable plasma platinum (UPt) were measured in the last three dose levels with atomic absorption spectrophotometry with Zeeman correction. The mean (s.d.) level for TPt for 6 weeks at 15, 20 and 25 mg m-2 day-1 was 0.76 (0.15), 0.78 (0.19) and 0.90 (0.22) mg l-1 for UPt 0.10 (0.03), 0.12 (0.02) and 0.20 (0.03) mg l-1 respectively. TPt concentration levelled off after 3 weeks. The mean (s.d.) CLTB for UPt was 281 +/- 21 ml min-1 and correlated with glomerular filtration rate (r = 0.61, P = 0.03). As estimated with the sigmoid Emax model defined by the Hill equation the percentage reduction in platelets correlated with the area under the curve for UPt (r = 0.77). The maximum tolerable dose of carboplatin with concomitant continuous 60 Gy radiotherapy is 25 mg m-2 day-1; the recommended dose for phase II or III studies is 20 mg m-2 day-1 day for 6 weeks.
对21例先前未接受过治疗、局部无法手术切除的非小细胞肺癌(NSCLC)患者进行了一项I期研究,采用门诊持续卡铂输注联合连续6周胸部放疗。卡铂的剂量范围为在最后21天(第一水平)、最后31天(第二水平)或放疗期的6周内(第三水平)为15mg/m²/天,之后在放疗的6周内为20或25mg/m²/天(第四和第五水平)。总放疗剂量为60Gy,每周5天,每天2Gy。前3例患者仅接受放疗,未使用卡铂。在最后两个剂量水平,接受20mg/m²/天的6例患者中有2例、接受25mg/m²/天的6例患者中有1例发生了WHO III/IV级白细胞减少和血小板减少(剂量限制性毒性),接受25mg/m²/天的3例患者均发生了上述情况。发生了1例端口周围局部感染和1例锁骨下静脉血栓形成。卡铂治疗似乎未影响肺部和食管的放疗毒性。21例患者中,1例完全缓解(CR),10例部分缓解(PR),6例病情稳定(SD),4例病情进展(PD)。在最后三个剂量水平,采用带塞曼校正的原子吸收分光光度法测量了总铂(TPt)和可超滤血浆铂(UPt)。在15、20和25mg/m²/天剂量水平下,6周内TPt的平均(标准差)水平分别为0.76(0.15)、0.78(0.19)和0.90(0.22)mg/L,UPt分别为0.10(0.03)、0.12(0.02)和0.20(0.03)mg/L。3周后TPt浓度趋于平稳。UPt的平均(标准差)CLTB为281±21ml/min,与肾小球滤过率相关(r=0.61,P=0.03)。根据希尔方程定义的S型Emax模型估计,血小板减少的百分比与UPt曲线下面积相关(r=0.77)。卡铂与连续60Gy放疗联合使用时的最大耐受剂量为25mg/m²/天;II期或III期研究的推荐剂量为20mg/m²/天,持续6周。