Prediction Model for Severe Thrombocytopenia Induced by Gemcitabine Plus Cisplatin Combination Therapy in Patients with Urothelial Cancer
| dc.contributor.author | Matsumoto, Noriaki | |
| dc.contributor.author | Mizuno, Tomohiro | |
| dc.contributor.author | Ando, Yosuke | |
| dc.contributor.author | Kato, Koki | |
| dc.contributor.author | Nakanishi, Masanori | |
| dc.contributor.author | Nakai, Tsuyoshi | |
| dc.contributor.author | Lee, Jeannie K. | |
| dc.contributor.author | Kameya, Yoshitaka | |
| dc.contributor.author | Nakamura, Wataru | |
| dc.contributor.author | Takahara, Kiyoshi | |
| dc.contributor.author | Shiroki, Ryoichi | |
| dc.contributor.author | Yamada, Shigeki | |
| dc.date.accessioned | 2024-06-05T19:11:19Z | |
| dc.date.available | 2024-06-05T19:11:19Z | |
| dc.date.issued | 2024-04-29 | |
| dc.identifier.citation | Matsumoto, N., Mizuno, T., Ando, Y. et al. Prediction Model for Severe Thrombocytopenia Induced by Gemcitabine Plus Cisplatin Combination Therapy in Patients with Urothelial Cancer. Clin Drug Investig 44, 357–366 (2024). https://doi.org/10.1007/s40261-024-01361-3 | en_US |
| dc.identifier.issn | 1173-2563 | |
| dc.identifier.doi | 10.1007/s40261-024-01361-3 | |
| dc.identifier.uri | http://hdl.handle.net/10150/672487 | |
| dc.description.abstract | Background: Chemotherapy-induced thrombocytopenia is often a use-limiting adverse reaction to gemcitabine and cisplatin (GC) combination chemotherapy, reducing therapeutic intensity, and, in some cases, requiring platelet transfusion. Objective: A retrospective cohort study was conducted on patients with urothelial cancer at the initiation of GC combination therapy and the objective was to develop a prediction model for the incidence of severe thrombocytopenia using machine learning. Methods: We performed receiver operating characteristic analysis to determine the cut-off values of the associated factors. Multivariate analyses were conducted to identify risk factors associated with the occurrence of severe thrombocytopenia. The prediction model was constructed from an ensemble model and gradient-boosted decision trees to estimate the risk of an outcome using the risk factors associated with the occurrence of severe thrombocytopenia. Results: Of 186 patients included in this study, 46 (25%) experienced severe thrombocytopenia induced by GC therapy. Multivariate analyses revealed that platelet count ≤ 21.4 (×104/µL) [odds ratio 7.19, p < 0.01], hemoglobin ≤ 12.1 (g/dL) [odds ratio 2.41, p = 0.03], lymphocyte count ≤ 1.458 (×103/µL) [odds ratio 2.47, p = 0.02], and dose of gemcitabine ≥ 775.245 (mg/m2) [odds ratio 4.00, p < 0.01] were risk factors of severe thrombocytopenia. The performance of the prediction model using these associated factors was high (area under the curve 0.76, accuracy 0.82, precision 0.68, recall 0.50, and F-measure 0.58). Conclusions: Platelet count, hemoglobin level, lymphocyte count, and gemcitabine dose contributed to the development of a novel prediction model to identify the incidence of GC-induced severe thrombocytopenia. | en_US |
| dc.description.sponsorship | Japan Society for the Promotion of Science | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer Science and Business Media LLC | en_US |
| dc.rights | © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024. | en_US |
| dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en_US |
| dc.title | Prediction Model for Severe Thrombocytopenia Induced by Gemcitabine Plus Cisplatin Combination Therapy in Patients with Urothelial Cancer | en_US |
| dc.type | Article | en_US |
| dc.identifier.eissn | 1179-1918 | |
| dc.contributor.department | Department of Pharmacy Practice and Science, R. Ken Coit College of Pharmacy, The University of Arizona | en_US |
| dc.identifier.journal | Clinical Drug Investigation | en_US |
| dc.description.note | 12 month embargo; first published 29 April 2024 | en_US |
| dc.description.collectioninformation | This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu. | en_US |
| dc.eprint.version | Final accepted manuscript | en_US |
| dc.identifier.pii | 1361 | |
| dc.source.journaltitle | Clinical Drug Investigation | |
| dc.source.volume | 44 | |
| dc.source.issue | 5 | |
| dc.source.beginpage | 357 | |
| dc.source.endpage | 366 |
