Population Pharmacokinetic Analyses and Exposure-Efficacy Relationships of Venetoclax in Chinese Pediatric Patients with Hematological Malignancy in a Real-World Setting.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · 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.
[BACKGROUND] Venetoclax (VEN), a selective B-cell lymphoma 2 (BCL-2) inhibitor, is used in pediatric hematologic malignancies.
- p-value p < 0.05
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 한글 요약
[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.
[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.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Sulfonamides
- Male
- Female
- Retrospective Studies
- Child
- Preschool
- Bridged Bicyclo Compounds
- Heterocyclic
- Antineoplastic Agents
- Infant
- Leukemia
- Myeloid
- Acute
- Adolescent
- Hematologic Neoplasms
- Dose-Response Relationship
- Drug
- China
- East Asian People
- hematological malignancy
- pediatric
- population pharmacokinetics
- venetoclax
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