Open Access
The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan
Y. ‐Y. Su
,
N J Chiang
,
J.S. Chang
,
Y. W. Wang
,
Bo Shen
,
Y. J. Li
,
D Y Hwang
,
Yan Shan
,
Li-Tzong Chen
Publication type: Journal Article
Publication date: 2023-02-01
PubMed ID:
36527823
Cancer Research
Oncology
Abstract
Initial dose adjustment is recommended for patients with known UGT1A1∗28 homozygosity for both conventional irinotecan and liposomal irinotecan (nal-IRI). A recent population pharmacokinetic (PK) study showed that Asian patients had a lower prevalence of UGT1A1∗28 homozygosity but a significantly higher maximum blood concentration of SN-38 (SN-38 Cmax) and a higher incidence of grade ≥3 neutropenia after nal-IRI administration than Caucasian patients. The current study investigated the association of UGT1A1 polymorphisms, including the Asian prevalent UGT1A1∗6, PK and toxicities of nal-IRI-based therapy in the Asian population.A total of 162 patients with nal-IRI-based therapy and available UGT1A1∗6 and UGT1A1∗28 genotyping were included, with 82 Asian patients from six previous phase I or II studies of nal-IRI (cohort 1) and another 80 patients with nal-IRI + 5-fluorouracil/leucovorin every 2 weeks as real-world practice in a single institute in Taiwan (cohort 2).The frequency of UGT1A1∗6 or UGT1A1∗28 homozygosity/compound heterozygosity was 9.3%, with UGT1A1∗6/∗6 in 2.5%, UGT1A1∗28/∗28 in 1.9% and UGT1A1∗6/∗28 in 4.9%. Among the 53 patients in cohort 1 with available PK data, all 7 patients with homozygosity/compound heterozygosity harbored UGT1A1∗6 and had a significantly higher level of median dose-normalized area under the concentration-time curve (AUC) and Cmax of SN-38 than those with single heterozygosity/wild type. Of the entire study population, the incidence of grade ≥3 neutropenia and diarrhea was significantly higher in patients with homozygosity/compound heterozygosity than in those with single heterozygosity/wild type, 73.3% versus 38.1% (P = 0.012, Fisher's exact test) and 33.3% versus 9.5% (P = 0.018, Fisher's exact test), respectively.The results suggest that the recommendation of a lower starting dose of nal-IRI for patients with UGT1A1∗28 homozygosity should be extended to include patients with UGT1A1∗6 homozygosity/compound heterozygosity.
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GOST
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Su Y. ‐. et al. The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan // ESMO Open. 2023. Vol. 8. No. 1. p. 100746.
GOST all authors (up to 50)
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Su Y. ‐., Chiang N. J., Chang J., Wang Y., Shen B., Li Y. J., Hwang D. Y., Shan Y., Chen L. The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan // ESMO Open. 2023. Vol. 8. No. 1. p. 100746.
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RIS
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TY - JOUR
DO - 10.1016/j.esmoop.2022.100746
UR - https://doi.org/10.1016/j.esmoop.2022.100746
TI - The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan
T2 - ESMO Open
AU - Su, Y. ‐Y.
AU - Chiang, N J
AU - Chang, J.S.
AU - Wang, Y. W.
AU - Shen, Bo
AU - Li, Y. J.
AU - Hwang, D Y
AU - Shan, Yan
AU - Chen, Li-Tzong
PY - 2023
DA - 2023/02/01
PB - Elsevier
SP - 100746
IS - 1
VL - 8
PMID - 36527823
SN - 2059-7029
ER -
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BibTex (up to 50 authors)
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@article{2023_Su,
author = {Y. ‐Y. Su and N J Chiang and J.S. Chang and Y. W. Wang and Bo Shen and Y. J. Li and D Y Hwang and Yan Shan and Li-Tzong Chen},
title = {The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan},
journal = {ESMO Open},
year = {2023},
volume = {8},
publisher = {Elsevier},
month = {feb},
url = {https://doi.org/10.1016/j.esmoop.2022.100746},
number = {1},
pages = {100746},
doi = {10.1016/j.esmoop.2022.100746}
}
Cite this
MLA
Copy
Su, Y. ‐Y., et al. “The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan.” ESMO Open, vol. 8, no. 1, Feb. 2023, p. 100746. https://doi.org/10.1016/j.esmoop.2022.100746.
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