Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia

被引:18
|
作者
Larsen, Rikke Hebo [1 ]
Rank, Cecilie Utke [1 ,2 ]
Grell, Kathrine [1 ,3 ]
Moller, Lisbeth Norgaard [1 ]
Overgaard, Ulrik Malthe [2 ]
Kampmann, Peter [2 ]
Nersting, Jacob [1 ]
Degn, Matilda [1 ]
Nielsen, Stine Nygaard [1 ]
Holst, Helle [1 ]
Albertsen, Birgitte Klug [4 ,5 ]
Wehner, Peder Skov [6 ]
Callesen, Michael Thude [6 ]
Kanerva, Jukka [7 ]
Frandsen, Thomas Leth [1 ]
Als-Nielsen, Bodil [1 ]
Hjalgrim, Lisa Lyngsie [1 ]
Schmiegelow, Kjeld [1 ,8 ]
机构
[1] Univ Copenhagen, Rigshosp, Dept Pediat & Adolescent Med, Copenhagen, Denmark
[2] Univ Copenhagen, Rigshosp, Dept Hematol, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Publ Hlth, Sect Biostat, Copenhagen, Denmark
[4] Aarhus Univ, Dept Pediat & Adolescent Med, Aarhus, Denmark
[5] Aarhus Univ, Dept Clin Med, Aarhus, Denmark
[6] Odense Univ Hosp, HC Andersen Childrens Hosp, Dept Pediat Hematol & Oncol, Odense, Denmark
[7] Univ Helsinki, Helsinki Univ Hosp, New Childrens Hosp, HUS, Helsinki, Finland
[8] Univ Copenhagen, Fac Med, Inst Clin Med, Copenhagen, Denmark
关键词
FASTING HYPOGLYCEMIA; NOPHO ALL2008; CHILDHOOD; CHILDREN; 6-THIOGUANINE; RELAPSE; RISK; 6-MERCAPTOPURINE; INTENSIFICATION; MERCAPTOPURINE;
D O I
10.3324/haematol.2020.278166
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maintenance therapy containing methotrexate and 6-mercaptopurine is essential to cure acute lymphoblastic leukemia (ALL). Cytotoxicity is elicited by incorporation of thioguanine nucleotides into DNA (DNA-TG), and higher leukocyte DNA-TG is associated with increased relapse-free survival. As 6-thioguanine provides 6-fold higher cytosolic levels of thioguanine nucleotides than does 6-mercaptopurine, we added low-dose 6-thioguanine to methotrexate/6-mercaptopurine maintenance therapy to explore if this combination results in significantly higher DNA-TG. The target population of the "Thiopurine Enhanced ALL Maintenance therapy" (TEAM) study was 30 patients with non-high-risk ALL, aged 1-45 years on methotrexate/6-mercaptopurine maintenance therapy receiving no other systemic chemotherapy. Incremental doses of 6-thioguanine were added to methotrexate/6-mercaptopurine maintenance therapy (starting 6-thioguanine dose: 2.5 mg/m(2)/day, maximum: 12.5 mg/m(2)/day). The primary endpoint was DNA-TG increments. Thirty-four patients were included, and 30 patients completed maintenance therapy according to the TEAM strategy. Of these 30 patients, 26 (87%) tolerated 10.0-12.5 mg/m(2)/day as the maximum 6-thioguanine dose. TEAM resulted in significantly higher DNA-TG levels compared to those in both TEAM patients before their inclusion in TEAM (on average 251 fmol/mu g DNA higher [95% confidence interval: 160-341; P<0.0001]), and with historical patients receiving standard methotrexate/6-mercaptopurine maintenance therapy (on average 272 fmol/mu g DNA higher [95% confidence interval: 147 398; P<0.0001]). TEAM did not increase myelotoxicity or hepatotoxicity. In conclusion, TEAM is an innovative and feasible approach to improve maintenance therapy and results in higher DNA-TG levels without inducing additional toxicity. It may therefore be an effective strategy to reduce the risk of ALL relapse through increased DNA-TG. This will be tested in a randomized ALLTogether-1 substudy.
引用
收藏
页码:2824 / 2833
页数:10
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