Laurence V M, Ward R, Dennis I F, Bleehen N M
MRC Unit, Addenbrookes Hospital, Cambridge, UK.
Br J Cancer. 1995 Jul;72(1):198-205. doi: 10.1038/bjc.1995.303.
Nicotinamide and carbogen breathing are both effective radiosensitisers in experimental tumour models and are even more effective in combination. This study was to investigate the feasibility of using the agents in combination in patients and to measure their effect on tumour oxygenation. Twelve patients with advanced malignant disease were treated with 4-6 g of oral nicotinamide (NCT) in tablet formulation. Ten of these 12 patients breathed carbogen (95% oxygen, 5% carbon dioxide) for up to 20 min at presumed peak plasma NCT concentration (Cpeak) and had tumour oxygen partial pressure (pO2) measured using the Eppendorf pO2) histograph. The mean Cpeak values were 82, 115 and 150 micrograms ml-1 for NCT doses of 4, 5 and 6 g respectively and were dose dependent. The time of Cpeak was independent of dose with an overall mean of 2.4 h (range 0.7-4 h). NCT toxicity occurred in 9 out of 12 patients and was mild in all but one; carbogen was well tolerated in all patients. Following NCT only two patients had significant rises (P < 0.05) in tumour median pO2. During carbogen breathing, eight out of ten patients had early highly significant rises in pO2 (P < 0.0001), of which six continued to rise or remained in plateau until completion of gas breathing. Six patients had hypoxic pretreatment values less than 5 mmHg, which were completely abolished in three and reduced in two during carbogen breathing. In conclusion, the combination of NCT and carbogen breathing was generally well tolerated and gave rise to substantial rises in tumour pO2 which were maintained throughout gas breathing. These results should encourage further study of this potentially useful combination of agents as radiosensitisers in the clinic.
烟酰胺和卡波金呼吸在实验性肿瘤模型中均为有效的放射增敏剂,二者联合使用时效果更佳。本研究旨在探讨在患者中联合使用这两种药物的可行性,并测定它们对肿瘤氧合的影响。12例晚期恶性疾病患者接受了口服片剂形式的4 - 6克烟酰胺(NCT)治疗。这12例患者中有10例在假定的血浆NCT浓度峰值(Cpeak)时呼吸卡波金(95%氧气,5%二氧化碳)长达20分钟,并使用Eppendorf pO2组织分析仪测量肿瘤氧分压(pO2)。NCT剂量为4克、5克和6克时,Cpeak的平均值分别为82、115和150微克/毫升,且呈剂量依赖性。Cpeak出现的时间与剂量无关,总体平均值为2.4小时(范围为0.7 - 4小时)。12例患者中有9例出现NCT毒性,除1例以外均为轻度;所有患者对卡波金的耐受性良好。仅使用NCT后,只有2例患者的肿瘤中位pO2有显著升高(P < 0.05)。在呼吸卡波金期间,10例患者中有8例的pO2早期有高度显著升高(P < 0.0001),其中6例在气体呼吸结束前持续升高或保持在平台期。6例患者预处理时的低氧值低于5 mmHg,在呼吸卡波金期间,3例患者的该值完全消除,2例患者的值降低。总之,NCT与卡波金呼吸联合使用总体耐受性良好,可使肿瘤pO2大幅升高,并在整个气体呼吸过程中保持。这些结果应促使进一步研究这种可能有用的联合药物作为临床放射增敏剂的应用。