Clinical implications of the Drug-Drug Interaction in Cancer Patients treated with innovative oncological treatments

被引:2
作者
Santamaria, Fiorenza [1 ,2 ]
Roberto, Michela [2 ]
Buccilli, Dorelsa [2 ,3 ]
Di Civita, Mattia Alberto [1 ,2 ,3 ]
Giancontieri, Paola [2 ,3 ]
Maltese, Giulia [2 ,3 ]
Nicolella, Francesco [2 ,3 ]
Torchia, Andrea [2 ,4 ]
Scagnoli, Simone [1 ,2 ]
Pisegna, Simona [1 ,2 ]
Barchiesi, Giacomo [2 ]
Speranza, Iolanda [2 ]
Botticelli, Andrea [2 ,3 ]
Santini, Daniele [2 ,5 ]
机构
[1] Sapienza Univ Rome, Dept Expt Med, Rome, Italy
[2] AOU Policlin Umberto 1, Dept Hematol Oncol & Dermatol, Med Oncol A, Rome, Italy
[3] Sapienza Univ Rome, Dept Radiol Oncol & Pathol Anat Sci, Rome, Italy
[4] Sapienza Univ Rome, Clin & Mol Med, Rome, Italy
[5] Sapienza Univ Rome, Dept Med Surg Sci & Biotechnol, Rome, Italy
关键词
Drug-Drug-Interactions; DDI; Cancer; Polypharmacy; Targeted therapy; Immunotherapy; PROTON PUMP INHIBITORS; BREAST; PHARMACOKINETICS; ABIRATERONE; OUTCOMES; PARP; PALBOCICLIB; MECHANISMS; THERAPY;
D O I
10.1016/j.critrevonc.2024.104405
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the last two-decades, innovative drugs have revolutionized cancer treatments, demonstrating a significant improvement in overall survival. These drugs may present several pharmacokinetics interactions with nononcological drugs, and vice versa, and, non-oncological drugs can modify oncological treatment outcome both with pharmacokinetic interaction and with an "off-target impact" on the tumor microenvironment or on the peripheral immune response. It's supposed that the presence of a drug-drug interaction (DDI) is associated with an increased risk of reduced anti-tumor effects or severe toxicities. However, clinical evidence that correlate the DDI presence with outcome are few, and results are difficult to compare because of difference in data collection and heterogeneous population. This review reports all the clinical evidence about DDI to provide an easy-to-use guide for DDI management and dose adjustment in solid tumors treated with inhibitors of the cyclin-dependent kinases CDK4-6, Antibody-drug conjugates, Poly ADPribose polymerase inhibitors, androgen-receptor targeted agents, or immunecheckpoints inhibitors.
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页数:16
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