Allopurinol Add‐on 6‐Mercaptopurine Strategy Improves Efficacy and Reduces Toxicity in Pediatric Patients With Acute Lymphoblastic Leukemia
The short-term efficacy of allopurinol add-on thiopurine therapy has been well documented; however, the long-term effects and dose recommendations are poorly detailed. This study aimed to elucidate the long-term implications of this combination therapy and to develop initial dose applying pharmacokinetic modeling. Forty-two pediatric patients with acute lymphoblastic leukemia, treated with 6-mercaptopurine (6-MP) and allopurinol, were enrolled in this prospective before-after pharmacokinetic study. Metabolite levels (6-thioguanine nucleotides (6-TGNs), methyl mercaptopurine nucleotides (6-MMPN), DNA-thioguanine (DNA-TG)), thiopurine methyltransferase (TPMT) activity were measured pre- and post-combination. Another retrospective cohort of 40 patients receiving 6-MP monotherapy was taken as controls. Compared with the control group, the combination therapy showed a similar myelosuppression effect ((P = 0.060, adjusted Hazard Rates, aHR = 0.94 (0.89-1.00)), while markedly reducing the cumulative hazard of severe neutropenia (P = 0.009, aHR = 0.49 (0.28-0.83)) and hepatotoxicity (P < 0.001, aHR = 0.54 (0.40-0.73)). Allopurinol combination led to a fourfold reduction in TPMT activity, the 6-MMPN:6-TGNs ratios, and 6-MMPN: DNA-TG ratios. This metabolic adjustment improved control of white blood cell (WBC) counts, neutrophil counts (ANC), and aminotransferase levels. LOESS regression estimates indicated significant fluctuations in WBC, ANC, and 6-MP/allopurinol dosage ratios following 3 months of combination therapy (P < 0.001), reflecting the need for close monitoring and frequent dose adjustments. Pharmacokinetic analysis further reinforces the benefits of allopurinol add-on 6-MP strategy, and suggested that, for patients with normal or high TPMT activity, an initial 6-MP dose of 20-30 mg/m<sup>2</sup>/day is recommended for those with BSA ≤ 1 m<sup>2</sup>, and 15-20 mg/m<sup>2</sup>/day for those with BSA > 1 m<sup>2</sup>, when co-administered with allopurinol (50 mg/m<sup>2</sup>/day).
Authors
- Xue‐Qun Luo (ORCID: https://orcid.org/0000-0001-8473-5343)
- Xueding Wang (ORCID: https://orcid.org/0000-0002-3580-9155)
- X. Zhang (ORCID: https://orcid.org/0009-0001-6819-023X)
- Yanping Guan (ORCID: https://orcid.org/0000-0002-4658-4318)
- Libin Huang (ORCID: https://orcid.org/0000-0001-8123-0235)
- Zhong Zuo (ORCID: https://orcid.org/0000-0002-6976-6157)
- Min Huang (ORCID: https://orcid.org/0000-0002-2844-5680)
- Ting Yang (ORCID: https://orcid.org/0000-0001-5875-5906)
- Dun‐hua Zhou (ORCID: https://orcid.org/0000-0002-8173-4924)
- S C Su (ORCID: https://orcid.org/0009-0001-6507-6933)
- Sumyuet Chan (ORCID: https://orcid.org/0009-0009-7697-7989)
- Qiaolan Xuan
Institutions
- Sun Yat-sen University (CN)
- Chinese University of Hong Kong (HK)
- Sun Yat-sen Memorial Hospital (CN)
- ShenZhen People’s Hospital (CN)
- Zero to Three (US)
- The First Affiliated Hospital, Sun Yat-sen University (CN)
Publication Details
- Journal
- Clinical Pharmacology & Therapeutics
- Published
- 2025-11-14
- DOI
- https://doi.org/10.1002/cpt.70123
- Primary Topic
- Acute Lymphoblastic Leukemia research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Guangdong Province
- Guangdong Provincial Key Laboratory of Construction Foundation
- National Key Research and Development Program of China