Armstrong Jonathan K, Hempel Georg, Koling Susanne, Chan Linda S, Fisher Timothy, Meiselman Herbert J, Garratty George
Department of Physiology and Biophysics, Keck School of Medicine, University of Southern California, Los Angeles, California 90033, USA.
Cancer. 2007 Jul 1;110(1):103-11. doi: 10.1002/cncr.22739.
Rapid clearance of poly(ethylene glycol)-asparaginase (PEG-ASNase) has been reported for up to one-third of patients treated for acute lymphoblastic leukemia (ALL), potentially rendering their treatment ineffective. A 25% occurrence of an antibody against PEG (anti-PEG) was previously reported in healthy blood donors. The objective of the study was to determine whether anti-PEG was associated with rapid clearance PEG-ASNase.
The investigation reanalyzed stored sera from pediatric patients enrolled in the ALL Berlin-Frankfurt-Muenster 2000 studies. Twenty-eight samples were selected to include 15 subjects with undetectable ASNase activity after receiving PEG-ASNase. Sixteen subjects treated with unmodified ASNase were also included, 8 with low ASNase activity. Sera were tested for anti-PEG using 2 techniques: 1) serology, by agglutination of PEG-coated red blood cells; 2) flow cytometry, by analysis of 10 microm PEG beads stained for bound immunoglobulins. RESULTS. Of the 15 sera from PEG-ASNase-treated patients with undetectable ASNase activity, anti-PEG was detected in 9 by serology and in 12 by flow cytometry. Anti-PEG was detected in 1 PEG-ASNase-treated patient with lower ASNase activity (123 U/L). No relation was observed between anti-PEG and serum ASNase activity for patients treated with unmodified ASNase.
The presence of anti-PEG was very closely associated with rapid clearance of PEG-ASNase. Further comprehensive studies are warranted to fully elucidate the effect of anti-PEG on PEG-conjugated agents. Screening and monitoring for anti-PEG may allow identification of patients for whom a modified dosing strategy or use of a non-PEGylated drug would be appropriate.
据报道,高达三分之一的急性淋巴细胞白血病(ALL)患者接受聚乙二醇天冬酰胺酶(PEG-ASNase)治疗后,该酶会迅速清除,这可能导致治疗无效。此前有报道称,健康献血者中抗聚乙二醇(anti-PEG)抗体的出现率为25%。本研究的目的是确定anti-PEG是否与PEG-ASNase的快速清除有关。
该调查重新分析了参与ALL柏林-法兰克福-明斯特2000研究的儿科患者的储存血清。选择了28个样本,其中包括15名接受PEG-ASNase治疗后天冬酰胺酶活性检测不到的受试者。还纳入了16名接受未修饰天冬酰胺酶治疗的受试者,其中8名天冬酰胺酶活性较低。使用两种技术检测血清中的anti-PEG:1)血清学方法,通过聚乙二醇包被的红细胞凝集反应;2)流式细胞术,通过分析标记有结合免疫球蛋白的10微米聚乙二醇微珠。结果。在15名接受PEG-ASNase治疗且天冬酰胺酶活性检测不到的患者的血清中,通过血清学方法在9份血清中检测到anti-PEG,通过流式细胞术在12份血清中检测到anti-PEG。在1名接受PEG-ASNase治疗且天冬酰胺酶活性较低(123 U/L)的患者中检测到anti-PEG。对于接受未修饰天冬酰胺酶治疗的患者,未观察到anti-PEG与血清天冬酰胺酶活性之间的关系。
anti-PEG的存在与PEG-ASNase的快速清除密切相关。有必要进行进一步的全面研究,以充分阐明anti-PEG对聚乙二醇偶联剂的影响。对抗PEG进行筛查和监测可能有助于识别适合采用调整剂量策略或使用非聚乙二醇化药物的患者。