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Population Pharmacokinetic Analyses and Exposure-Efficacy Relationships of Venetoclax in Chinese Pediatric Patients with Hematological Malignancy in a Real-World Setting.

1/5 보강
Drug design, development and therapy 📖 저널 OA 100% 2022: 1/1 OA 2023: 1/1 OA 2024: 2/2 OA 2025: 40/40 OA 2026: 37/37 OA 2022~2026 2026 Vol.20() p. 583847 OA
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
96 patients using nonlinear mixed-effects (NLME) modeling in Phoenix NLME software.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] This study establishes the first real-world population pharmacokinetic model of venetoclax in Chinese pediatric patients and demonstrates a clinically meaningful exposure-response relationship. The positive association between VEN exposure and MRD negativity supports the use of therapeutic drug monitoring and PPK-guided dosing to optimize treatment in pediatric AML.

Zhao Y, Song X, Zhang L, Zhu Y, Chen J, Gong Y

📝 환자 설명용 한 줄

[BACKGROUND] Venetoclax (VEN), a selective B-cell lymphoma 2 (BCL-2) inhibitor, is used in pediatric hematologic malignancies.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p < 0.05

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↓ .bib ↓ .ris
APA Zhao Y, Song X, et al. (2026). Population Pharmacokinetic Analyses and Exposure-Efficacy Relationships of Venetoclax in Chinese Pediatric Patients with Hematological Malignancy in a Real-World Setting.. Drug design, development and therapy, 20, 583847. https://doi.org/10.2147/DDDT.S583847
MLA Zhao Y, et al.. "Population Pharmacokinetic Analyses and Exposure-Efficacy Relationships of Venetoclax in Chinese Pediatric Patients with Hematological Malignancy in a Real-World Setting.." Drug design, development and therapy, vol. 20, 2026, pp. 583847.
PMID 41884469 ↗

Abstract

[BACKGROUND] Venetoclax (VEN), a selective B-cell lymphoma 2 (BCL-2) inhibitor, is used in pediatric hematologic malignancies. Research on individualized VEN therapy in Chinese pediatric patients remains limited. This study aimed to develop a population pharmacokinetic (PPK) model in Chinese pediatric patients, identify covariates influencing pharmacokinetics, support personalized dosing, and explore exposure-efficacy relationships in pediatric acute myeloid leukemia (AML).

[METHODS] PPK modeling was based on 225 plasma concentrations from 96 patients using nonlinear mixed-effects (NLME) modeling in Phoenix NLME software. A retrospective cohort of 52 AML patients receiving VEN with hypomethylating agents was analyzed, grouped as newly diagnosed or relapsed/refractory (R/R). Minimal residual disease (MRD) negativity was the primary endpoint. Mann-Whitney -tests and logistic regression assessed associations between trough concentration (C) and 6-hour post-dose concentration (C) levels and MRD status.

[RESULTS] A one-compartment model best described the pharmacokinetics of VEN. Body surface area (BSA) and the use of triazole drugs significantly influenced apparent clearance (CL/F), while total protein (TP) had a significant impact on apparent volume of distribution (V/F). The final model estimates were: ka = 0.15 h (fixed), V/F = 124.7 L, CL/F = 4.8 L⋅h. In both newly diagnosed and R/R AML patients, C and C concentrations were significantly higher in the MRD-negative group than in the MRD-positive group (all p < 0.05). Exposure-response analyses demonstrated a consistent positive association between higher VEN exposure and MRD negativity. Logistic regression further confirmed that both C and C were independent predictors of achieving MRD negativity. Notably, in the R/R cohort, higher C exposure quartiles were significantly associated with increased MRD-negative rates.

[CONCLUSION] This study establishes the first real-world population pharmacokinetic model of venetoclax in Chinese pediatric patients and demonstrates a clinically meaningful exposure-response relationship. The positive association between VEN exposure and MRD negativity supports the use of therapeutic drug monitoring and PPK-guided dosing to optimize treatment in pediatric AML.

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