| Literature DB >> 19768519 |
Shizuka Watanabe1,2,3, Kumiko Miyake1,3, Chitose Ogawa1, Haruna Matsumoto1,3, Kenichi Yoshida1, Shinsuke Hirabayashi1, Daisuke Hasegawa1, Tadao Inoue4, Junko Kizu3, Reiko Machida5, Akira Ohara5, Ryota Hosoya1, Atsushi Manabe6.
Abstract
Patients with acute lymphoblastic leukemia (ALL), who develop antiasparaginase antibodies without clinical allergic reactions ("silent inactivation") during L: -asparaginase (L: -Asp) treatment, have poor outcomes. Ammonia is produced by hydrolysis of asparagine by L: -Asp. We postulated that plasma ammonia level might reflect the biological activity of L: -Asp. Five children with ALL treated according to the Tokyo Children's Cancer Study Group (TCCSG) protocol were enrolled. Plasma ammonia levels were analyzed immediately and 1 h after incubation at room temperature and "ex vivo ammonia production" was defined as increase in ammonia concentration. Ex vivo ammonia production well correlated with L: -Asp activity (r = 0.882, P < 0.01, n = 23). It always exceeded 170 microg/dL (170-345 microg/dL) in induction therapy. We found 3 patients whose ammonia production was negligible during later phases of therapy. Antiasparaginase antibody was detected and L: -Asp activity decreased in these patients. Ex vivo ammonia production is a surrogate marker of L: -Asp biological activity.Entities:
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Year: 2009 PMID: 19768519 DOI: 10.1007/s12185-009-0419-x
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490