Barone Raffaella, Pauwels Stanislas, De Camps Joëlle, Krenning Eric P, Kvols Larry K, Smith M Charles, Bouterfa Hakim, Devuyst Olivier, Jamar François
Center of Nuclear Medicine, University of Louvain Medical School, UCL 54.30, Avenue Hippocrate, 54, B-1200 Brussels, Belgium.
Nephrol Dial Transplant. 2004 Sep;19(9):2275-81. doi: 10.1093/ndt/gfh362. Epub 2004 Jul 13.
Infusion of amino acids (AAs) can reduce renal uptake of radiolabelled somatostatin analogues resulting in a lower kidney exposure during peptide radiotherapy of patients with neuroendocrine tumours. In this study, we investigated the metabolic effects related to the infusion of large amounts of amino acids in patients undergoing positron emission tomography (PET) studies with [(86)Y]DOTA(0)-D-Phe(1)-Tyr(3)-octreotide.
Twenty-four patients, in four consecutive groups of six, received a 4 h infusion of 120 g of mixed AAs and, in addition, either a 4 h infusion of 50 g of L-lysine (n = 6), a 10 h infusion of 240 g of mixed AAs (n = 6), a 4 h infusion of 50 g of L-lysine + L-arginine (Lys-Arg; n = 6) or no infusion (control; n = 6) in randomly ordered crossover studies. A number of clinical and biochemical parameters in blood and urine were measured over 24 h, including calculation of creatinine clearance, tubular reabsorption of inorganic phosphate (TRP) and fractional urate excretion.
No clinical side effects occurred during the infusions except for nausea and vomiting under mixed AAs. Patients in the latter group showed an increase in serum urea, whereas patients receiving L-lysine showed an increase in serum potassium and chloride. Inorganic phosphate levels dropped at 2.5 h in all groups except controls, and a significant decrease in TRP was observed with mixed AAs but not with L-lysine or Lys-Arg.
Although infusion of AA solutions can improve the effect of therapy by allowing the administration of higher doses of radiolabelled somatostatin analogues, each preparation has specific sides effects that should be taken into account with this type of therapy.
输注氨基酸(AAs)可减少放射性标记的生长抑素类似物的肾脏摄取,从而在神经内分泌肿瘤患者的肽类放射治疗期间降低肾脏暴露量。在本研究中,我们调查了接受[(86)Y]DOTA(0)-D-Phe(1)-Tyr(3)-奥曲肽正电子发射断层扫描(PET)研究的患者中,与输注大量氨基酸相关的代谢效应。
24名患者分为连续4组,每组6人,接受4小时输注120克混合氨基酸,此外,在随机顺序交叉研究中,分别接受4小时输注50克L-赖氨酸(n = 6)、10小时输注240克混合氨基酸(n = 6)、4小时输注50克L-赖氨酸 + L-精氨酸(Lys-Arg;n = 6)或不输注(对照组;n = 6)。在24小时内测量血液和尿液中的一些临床和生化参数,包括计算肌酐清除率、无机磷酸盐的肾小管重吸收(TRP)和尿酸排泄分数。
输注期间除混合氨基酸组出现恶心和呕吐外,未发生临床副作用。后一组患者的血清尿素升高,而接受L-赖氨酸的患者血清钾和氯升高。除对照组外,所有组在2.5小时时无机磷酸盐水平均下降,混合氨基酸组观察到TRP显著降低,而L-赖氨酸或Lys-Arg组未观察到。
尽管输注氨基酸溶液可通过允许给予更高剂量的放射性标记生长抑素类似物来改善治疗效果,但每种制剂都有特定的副作用,在这类治疗中应予以考虑。