Difference between revisions of "Lenvatinib (Lenvima)"

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==History of changes in Health Canada indication==
 
==History of changes in Health Canada indication==
 
*2019-09-20: Notice of compliance with conditions in combination with pembrolizumab, for the treatment of adult patients with advanced [[Endometrial cancer|endometrial carcinoma]] that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR), who have disease progression following prior platinum-based systemic therapy, and are not candidates for curative surgery or radiation.
 
*2019-09-20: Notice of compliance with conditions in combination with pembrolizumab, for the treatment of adult patients with advanced [[Endometrial cancer|endometrial carcinoma]] that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR), who have disease progression following prior platinum-based systemic therapy, and are not candidates for curative surgery or radiation.
 
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==History of changes in PMDA indication==
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*2021-12-24: new indication and a new dosage for the treatment of unresectable advanced or recurrent [[Endometrial cancer|endometrial carcinoma]] that has progressed after cancer chemotherapy.
 
==Also known as==
 
==Also known as==
 
*'''Code name:''' E7080
 
*'''Code name:''' E7080

Revision as of 20:54, 6 June 2023

General information

Class/mechanism: Tyrosine kinase inhibitor of multiple receptor tyrosine kinases (RTKs), including: vascular endothelial growth factor (VEGF) receptors VEGFR1 (FLT1), VEGFR2 (KDR), and VEGFR3 (FLT4); fibroblast growth factor (FGF) receptors FGFR1, FGFR2, FGFR3, and FGFR4; platelet derived growth factor receptor alpha (PDGFRα), KIT, and RET. Inhibition of these receptor tyrosine kinases interferes with cancer cells' proliferation and pathogenic angiogenesis.[1][2][3]
Route: PO
Extravasation: n/a

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the package insert.[1]

Diseases for which it is established

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Differentiated thyroid cancer

  • 2015-02-13: Approved for the treatment of patients with locally recurrent or metastatic, progressive, radioactive iodine-refractory differentiated thyroid cancer. (Initial approval; based on SELECT)

Endometrial cancer

  • 2019-09-17: Accelerated approval in combination with Pembrolizumab (Keytruda) for the treatment of patients with advanced endometrial carcinoma that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) and who have disease progression following prior systemic therapy but are not candidates for curative surgery or radiation. (Based on KEYNOTE-146)
    • 2021-07-21: Converted to regular approval in combination with Pembrolizumab (Keytruda) for the treatment of patients with advanced endometrial carcinoma that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) and who have disease progression following prior systemic therapy but are not candidates for curative surgery or radiation. (Based on KEYNOTE-775)

Hepatocellular carcinoma

Renal cell carcinoma

History of changes in EMA indication

  • 2015-05-28: Initial authorization as Lenvima
  • 2016-08-25: Initial authorization as Kisplyx

Differentiated thyroid cancer

Hepatocellular carcinoma

  • Lenvima is indicated as monotherapy for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (HCC) who have received no prior systemic therapy.

History of changes in Health Canada indication

  • 2019-09-20: Notice of compliance with conditions in combination with pembrolizumab, for the treatment of adult patients with advanced endometrial carcinoma that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR), who have disease progression following prior platinum-based systemic therapy, and are not candidates for curative surgery or radiation.

History of changes in PMDA indication

  • 2021-12-24: new indication and a new dosage for the treatment of unresectable advanced or recurrent endometrial carcinoma that has progressed after cancer chemotherapy.

Also known as

  • Code name: E7080
  • Brand name: Kisplyx, Lenvima

References