Arruebo M, Vilaboa N, Sáez-Gutierrez B, Lambea J, Tres A, Valladares M et al. Assessment of the evolution of cancer treatment therapies. Cancers (Basel). 2011;3(3):3279-330. doi:10.3390/cancers3033279.
Gerber DE. Targeted therapies: a new generation of cancer treatments. American Family Physician. 2008;77(3):311-9.
Bhullar KS, Lagarón NO, McGowan EM, Parmar I, Jha A, Hubbard BP et al. Kinase-targeted cancer therapies: progress, challenges and future directions. Mol Cancer. 2018;17(1):48-. doi:10.1186/s12943-018-0804-2.
van Erp NP, Gelderblom H, Guchelaar H-J. Clinical pharmacokinetics of tyrosine kinase inhibitors. Cancer Treatment Reviews. 2009;35(8):692-706. doi:https://doi.org/10.1016/j.ctrv.2009.08.004.
Roninson IB. The role of the MDR1 (p-glycoprotein) gene in multidrug resistance in vitro and in vivo. Biochemical Pharmacology. 1992;43(1):95-102. doi:https://doi.org/10.1016/0006-2952(92)90666-7.
Nakanishi T, Ross DD. Breast cancer resistance protein (BCRP/ABCG2): its role in multidrug resistance and regulation of its gene expression. Chin J Cancer. 2012;31(2):73-99. doi:10.5732/cjc.011.10320.
Li W, Sparidans RW, Wang Y, Lebre MC, Beijnen JH, Schinkel AH. Oral coadministration of elacridar and ritonavir enhances brain accumulation and oral availability of the novel ALK/ROS1 inhibitor lorlatinib. European Journal of Pharmaceutics and Biopharmaceutics. 2019;136:120-30. doi:https://doi.org/10.1016/j.ejpb.2019.01.016.
Lheureux S, Denoyelle C, Ohashi PS, De Bono JS, Mottaghy FM. Molecularly targeted therapies in cancer: a guide for the nuclear medicine physician. Eur J Nucl Med Mol Imaging. 2017;44(Suppl 1):41-54. doi:10.1007/s00259-017-3695-3.
Weisberg E, Manley PW, Cowan-Jacob SW, Hochhaus A, Griffin JD. Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia. Nature Reviews Cancer. 2007;7:345. doi:10.1038/nrc2126.
Della Corte CM, Viscardi G, Di Liello R, Fasano M, Martinelli E, Troiani T et al. Role and targeting of anaplastic lymphoma kinase in cancer. Mol Cancer. 2018;17(1):30-. doi:10.1186/s12943-018-0776-2.
Huang H. Anaplastic Lymphoma Kinase (ALK) Receptor Tyrosine Kinase: A Catalytic Receptor with Many Faces. Int J Mol Sci. 2018;19(11):3448. doi:10.3390/ijms19113448.
Wu J, Savooji J, Liu D. Second- and third-generation ALK inhibitors for non-small cell lung cancer. Journal of Hematology & Oncology. 2016;9(1):19. doi:10.1186/s13045-016-0251-8.
Muller IB, de Langen AJ, Giovannetti E, Peters GJ. Anaplastic lymphoma kinase inhibition in metastatic non-small cell lung cancer: clinical impact of alectinib. Onco Targets Ther. 2017;10:4535-41. doi:10.2147/OTT.S109493.
Pfizer Labs. FULL PRESCRIBING INFORMATION. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/202570s021lbl.pdf: Reference ID: 4127887; 2017.
Novartis Pharma GmbH. SUMMARY OF PRODUCT CHARACTERISTICS. https://www.ema.europa.eu/en/documents/product-information/zykadia-epar-product-information_en.pdf 2017.
Rothenstein JM, Letarte N. Managing treatment-related adverse events associated with Alk inhibitors. Curr Oncol. 2014;21(1):19-26. doi:10.3747/co.21.1740.
Nix NM, Brown KS. Ceritinib for ALK-Rearrangement-Positive Non-Small Cell Lung Cancer. J Adv Pract Oncol. 2015;6(2):156-60.
Takeda Pharma A/S. SUMMARY OF PRODUCT CHARACTERISTICS. https://www.ema.europa.eu/en/documents/product-information/alunbrig-epar-product-information_en.pdf 2018.
Pfizer Labs. FULL PRESCRIBING INFORMATION https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210868s000lbl.pdf Reference ID: 4344940; 2018.
Roche Pharma AG. SUMMARY OF PRODUCT CHARACTERISTICS. https://www.ema.europa.eu/en/documents/product-information/alecensa-epar-product-information_en.pdf 2017.
Hirota T, Muraki S, Ieiri I. Clinical Pharmacokinetics of Anaplastic Lymphoma Kinase Inhibitors in Non-Small-Cell Lung Cancer. Clinical Pharmacokinetics. 2019;58(4):403-20. doi:10.1007/s40262-018-0689-7.
Katayama R. Drug resistance in anaplastic lymphoma kinase-rearranged lung cancer. Cancer Science. 2018;109(3):572-80. doi:10.1111/cas.13504.
Drilon A, Nagasubramanian R, Blake JF, Ku N, Tuch BB, Ebata K et al. A Next-Generation TRK Kinase Inhibitor Overcomes Acquired Resistance to Prior TRK Kinase Inhibition in Patients with TRK Fusion-Positive Solid Tumors. Cancer Discov. 2017;7(9):963-72. doi:10.1158/2159-8290.CD-17-0507.
Khotskaya YB, Holla VR, Farago AF, Mills Shaw KR, Meric-Bernstam F, Hong DS. Targeting TRK family proteins in cancer. Pharmacology & Therapeutics. 2017;173:58-66. doi:https://doi.org/10.1016/j.pharmthera.2017.02.006.
Ricciuti B, Genova C, Crinò L, Libra M, Leonardi GC. Antitumor activity of larotrectinib in tumors harboring NTRK gene fusions: a short review on the current evidence. Onco Targets Ther. 2019;12:3171-9. doi:10.2147/OTT.S177051.
Loxo Oncology. FULL PRESCRIBING INFORMATION. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/210861Orig1s000_21171Orig1s000Lbl.pdf: Reference ID: 4354324; 11.2018.
Akamine T, Toyokawa G, Tagawa T, Yamazaki K, Seto T, Takeo S et al. Lorlatinib for the treatment of patients with non-small cell lung cancer. Drugs of Today. 2019;55:107. doi:10.1358/dot.2019.55.2.2927983.
Sparidans RW, Li W, Schinkel AH, Beijnen JH. Bioanalytical assay for the novel TRK inhibitor selitrectinib in mouse plasma and tissue homogenates using liquid chromatography-tandem mass spectrometry. Journal of Chromatography B. 2019;1122-1123:78-82. doi:https://doi.org/10.1016/j.jchromb.2019.05.026.
Herbst RS. Review of epidermal growth factor receptor biology. International Journal of Radiation Oncology*Biology*Physics. 2004;59(2, Supplement):S21-S6. doi:https://doi.org/10.1016/j.ijrobp.2003.11.041.
Seshacharyulu P, Ponnusamy MP, Haridas D, Jain M, Ganti AK, Batra SK. Targeting the EGFR signaling pathway in cancer therapy. Expert Opin Ther Targets. 2012;16(1):15-31. doi:10.1517/14728222.2011.648617.
Oda K, Matsuoka Y, Funahashi A, Kitano H. A comprehensive pathway map of epidermal growth factor receptor signaling. Mol Syst Biol. 2005;1:2005.0010-2005.0010. doi:10.1038/msb4100014.
Takeda M, Nakagawa K. First- and Second-Generation EGFR-TKIs Are All Replaced to Osimertinib in Chemo-Naive EGFR Mutation-Positive Non-Small Cell Lung Cancer? Int J Mol Sci. 2019;20(1):146. doi:10.3390/ijms20010146.
OSI Pharmaceuticals Inc. FULL PRESCRIBING INFORMATION https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021743s14s16lbl.pdf2010.
AstraZeneca Pharmaceuticals LP. FULL PRESCRIBING INFORMATION https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/206995s003lbl.pdf Reference ID: 4310729 2018.
AstraZeneca Pharmaceuticals. FULL PRESCRIBING INFORMATION. https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/208065s008lbl.pdf 2018.
Smith J. Erlotinib: Small-molecule targeted therapy in the treatmentof non-small-cell lung cancer. Clinical Therapeutics. 2005;27(10):1513-34. doi:https://doi.org/10.1016/j.clinthera.2005.10.014.
Kucharczuk CR, Ganetsky A, Vozniak JM. Drug-Drug Interactions, Safety, and Pharmacokinetics of EGFR Tyrosine Kinase Inhibitors for the Treatment of Non-Small Cell Lung Cancer. J Adv Pract Oncol. 2018;9(2):189-200.
Pfizer Europe MA EEIG. FULL PRESCRIBING INFORMATION https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/211288s000lbl.pdf Reference ID: 4327054 2018.
Peters S, Zimmermann S, Adjei AA. Oral epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of non-small cell lung cancer: Comparative pharmacokinetics and drug–drug interactions. Cancer Treatment Reviews. 2014;40(8):917-26. doi:https://doi.org/10.1016/j.ctrv.2014.06.010.
Gao X, Le X, Costa DB. The safety and efficacy of osimertinib for the treatment of EGFR T790M mutation positive non-small-cell lung cancer. Expert Rev Anticancer Ther. 2016;16(4):383-90. doi:10.1586/14737140.2016.1162103.
Wind S, Schnell D, Ebner T, Freiwald M, Stopfer P. Clinical Pharmacokinetics and Pharmacodynamics of Afatinib. Clinical pharmacokinetics. 2017;56(3):235-50. doi:10.1007/s40262-016-0440-1.
Getov I, Grigorov E, Naseva E, Kojnov K. Model Pharmacoeconomic Study on Iressa® (Gefitinib) as a First Line Treatment of Non-Small Cell Lung Cancer at Stage IIIB/IV in EGFR Mutation Positive Bulgarian Patients. Biotechnol & Biotechnol Eq. 2013;27(1):3586-94. doi:10.5504/bbeq.2012.0050. .
Murtuza A, Bulbul A, Shen JP, Keshavarzian P, Woodward BD, Lopez-Diaz FJ et al. Novel Third-Generation EGFR Tyrosine Kinase Inhibitors and Strategies to Overcome Therapeutic Resistance in Lung Cancer. Cancer Research. 2019;79(4):689. doi:10.1158/0008-5472.CAN-18-1281.
Dai S, Zhou Z, Chen Z, Xu G, Chen Y. Fibroblast Growth Factor Receptors (FGFRs): Structures and Small Molecule Inhibitors. Cells. 2019;8(6):614. doi:10.3390/cells8060614.
Ornitz DM, Itoh N. The Fibroblast Growth Factor signaling pathway. Wiley Interdiscip Rev Dev Biol. 2015;4(3):215-66. doi:10.1002/wdev.176.
Janssen Pharmaceutical. FULL PRESCRIBING INFORMATION https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212018s000lbl.pdf Reference ID: 4418725; 2019.