Difference between revisions of "Ramucirumab (Cyramza)"
Warner-admin (talk | contribs) m (Text replacement - "[http://online.lexi.com/ Lexicomp]" to "Lexicomp") |
|||
(38 intermediate revisions by 3 users not shown) | |||
Line 1: | Line 1: | ||
==General information== | ==General information== | ||
− | Class/mechanism: Recombinant human IgG1 monoclonal antibody, VEGFR2 (vascular endothelial growth factor receptor 2) antagonist. Ramucirumab binds VEGFR2 and blocks VEGFR ligands, VEGF-A, VEGF-C, and VEGF-D, which inhibits angiogenesis.<ref name=insert>[http://pi.lilly.com/us/cyramza-pi.pdf Ramucirumab (Cyramza) package insert]</ref><ref>[[ | + | Class/mechanism: Recombinant human IgG1 monoclonal antibody, VEGFR2 (vascular endothelial growth factor receptor 2) antagonist. Ramucirumab binds VEGFR2 and blocks VEGFR ligands, VEGF-A, VEGF-C, and VEGF-D, which inhibits angiogenesis.<ref name=insert>[http://pi.lilly.com/us/cyramza-pi.pdf Ramucirumab (Cyramza) package insert]</ref><ref>[[:File:Ramucirumab.pdf | Ramucirumab (Cyramza) package insert (locally hosted backup)]]</ref><ref>[http://www.cyramzahcp.com/ Cyramza manufacturer's website]</ref> |
<br>Route: IV | <br>Route: IV | ||
<br>Extravasation: no information | <br>Extravasation: no information | ||
− | 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. | + | 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, [http://www.utdol.com/online/content/search.do UpToDate (courtesy of Lexicomp)], or the prescribing information.<ref name="insert"></ref> |
− | ==Diseases for which it is | + | ==Diseases for which it is established ''(work in progress)''== |
− | *[[ | + | *[[Colorectal cancer]] |
*[[Gastric cancer]] | *[[Gastric cancer]] | ||
+ | *[[Hepatocellular carcinoma]] | ||
*[[Non-small cell lung cancer]] | *[[Non-small cell lung cancer]] | ||
+ | |||
+ | ==Diseases for which it is used== | ||
+ | *[[Esophageal adenocarcinoma]] | ||
+ | *[[Urothelial carcinoma]] | ||
==Patient drug information== | ==Patient drug information== | ||
− | *[ | + | *[https://chemocare.com/druginfo/ramucirumab.aspx Ramucirumab (Cyramza) patient drug information (Chemocare)]<ref>[https://chemocare.com/druginfo/ramucirumab.aspx Ramucirumab (Cyramza) patient drug information (Chemocare)]</ref> |
*[http://pi.lilly.com/us/cyramza-pi.pdf Ramucirumab (Cyramza) package insert]<ref name="insert"></ref> | *[http://pi.lilly.com/us/cyramza-pi.pdf Ramucirumab (Cyramza) package insert]<ref name="insert"></ref> | ||
*[http://www.uptodate.com/contents/ramucirumab-patient-drug-information Ramucirumab (Cyramza) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/ramucirumab-patient-drug-information Ramucirumab (Cyramza) patient drug information (UpToDate)]</ref> | *[http://www.uptodate.com/contents/ramucirumab-patient-drug-information Ramucirumab (Cyramza) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/ramucirumab-patient-drug-information Ramucirumab (Cyramza) patient drug information (UpToDate)]</ref> | ||
==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
− | * | + | ===[[Colorectal cancer]]=== |
− | * 11 | + | * 2015-04-24: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm444496.htm Approved] in combination with [[Colon_cancer#FOLFIRI_.26_Ramucirumab|FOLFIRI]], for the treatment of metastatic [[colorectal cancer]] with disease progression on or after prior therapy with [[Bevacizumab (Avastin)|bevacizumab]], [[Oxaliplatin (Eloxatin)|oxaliplatin]], and a fluoropyrimidine. ''(New disease entity; based on RAISE)'' |
− | * 12 | + | |
− | * | + | ===[[Gastric cancer]]=== |
+ | * 2014-04-21: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm394260.htm Initial approval] for the treatment of patients with advanced or metastatic, [[Gastric cancer | gastric or gastroesophageal junction (GEJ) adenocarcinoma]] with disease progression on or after prior treatment with [[Regimen_classes#Fluoropyrimidine-based_regimen|fluoropyrimidine-]] or [[Regimen_classes#Platinum-based_regimen|platinum-]] containing chemotherapy. ''(Based on REGARD)'' | ||
+ | * 2014-11-05: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm421930.htm Approval and indication expanded] for use in combination with [[Paclitaxel (Taxol) | paclitaxel]] for the treatment of patients with advanced [[Gastric cancer | gastric or gastroesophageal junction (GEJ) adenocarcinoma]]. ''(Requirement for prior lines of treatment removed; based on RAINBOW)'' | ||
+ | |||
+ | ===[[Hepatocellular carcinoma]]=== | ||
+ | * 2019-05-10: Approved as a single agent for [[Hepatocellular carcinoma|hepatocellular carcinoma (HCC)]] in patients who have an [[Biomarkers#AFP|alpha fetoprotein (AFP)]] of at least 400 ng/mL and have been previously treated with sorafenib. ''(New disease entity; based on REACH-2)'' | ||
+ | |||
+ | ===[[Non-small cell lung cancer]]=== | ||
+ | * 2014-12-12: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm426735.htm Approved] for use in combination with [[Docetaxel (Taxotere)|docetaxel]] for the treatment of patients with metastatic [[Non-small cell lung cancer | non-small cell lung cancer (NSCLC)]] with disease progression on or after [[Regimen_classes#Platinum-based_regimen|platinum-based chemotherapy]]. ''(New disease entity; based on REVEL)'' | ||
+ | * 2020-05-29: Approved in combination with erlotinib for first-line treatment of metastatic [[Non-small cell lung cancer | non-small cell lung cancer (NSCLC)]] with [[Biomarkers#EGFR|epidermal growth factor receptor (EGFR)]] [[Biomarkers#Exon_19|exon 19]] [[#Biomarkers_Structural Variant|deletions]] or [[Biomarkers#L858R|exon 21 (L858R) mutations]]. ''(Approval expanded to first-line setting in EGFR+ NSCLC; based on RELAY)'' | ||
+ | |||
+ | ==History of changes in EMA indication== | ||
+ | *2014-12-16: Initial marketing authorization as Cyramza. | ||
+ | |||
+ | ==History of changes in Health Canada indication== | ||
+ | *2015-07-16: Initial notice of compliance as a single agent for the treatment of patients with advanced or metastatic [[gastric cancer]] or gastro-esophageal junction adenocarcinoma with disease progression on or after prior platinum and fluoropyrimidine chemotherapy. | ||
+ | *2015-07-16: Initial notice of compliance in combination with paclitaxel for the treatment of patients with advanced or metastatic [[gastric cancer]] or gastro-esophageal junction adenocarcinoma with disease progression on or after prior platinum and fluoropyrimidine chemotherapy. | ||
+ | ==History of changes in PMDA indication== | ||
+ | *2015-03-26: Initial approval for the treatment of unresectable advanced or recurrent [[gastric cancer]]. | ||
+ | *2016-05-23: New additional indication and a new dosage for the treatment of unresectable advanced or recurrent [[colorectal cancer]]. | ||
+ | *2016-06-20: New additional indication and a new dosage for the treatment of unresectable advanced/relapsed [[non-small cell lung cancer]]. | ||
+ | *2019-06-18: New indication for the treatment of patients with unresectable [[hepatocellular carcinoma]] whose serum AFP level is greater than 400 ng/mL and conditions have progressed after cancer chemotherapy. | ||
==Also known as== | ==Also known as== | ||
− | IMC-1121B | + | *'''Code names:''' IMC-1121B, LY-3009806 |
+ | *'''Brand name:''' Cyramza | ||
==References== | ==References== | ||
<references/> | <references/> | ||
− | [[Category: | + | [[Category:Drugs]] |
− | [[Category: | + | [[Category:Intravenous medications]] |
− | [[Category: | + | [[Category:Mutation-specific medications]] |
+ | [[Category:Protein expression-specific medications]] | ||
− | + | [[Category:Anti-VEGFR antibodies]] | |
− | [[Category:Anti- | + | [[Category:VEGFR inhibitors]] |
− | [[Category: | ||
− | [[Category: | + | [[Category:Colorectal cancer medications]] |
+ | [[Category:Esophageal adenocarcinoma medications]] | ||
[[Category:Gastric cancer medications]] | [[Category:Gastric cancer medications]] | ||
+ | [[Category:Hepatocellular carcinoma medications]] | ||
[[Category:Non-small cell lung cancer medications]] | [[Category:Non-small cell lung cancer medications]] | ||
− | [[Category: | + | [[Category:Urothelial carcinoma medications]] |
+ | |||
+ | [[Category:EMA approved in 2014]] | ||
+ | [[Category:FDA approved in 2014]] | ||
+ | [[Category:Health Canada approved in 2015]] | ||
+ | [[Category:PMDA approved in 2015]] |
Latest revision as of 12:08, 29 June 2024
General information
Class/mechanism: Recombinant human IgG1 monoclonal antibody, VEGFR2 (vascular endothelial growth factor receptor 2) antagonist. Ramucirumab binds VEGFR2 and blocks VEGFR ligands, VEGF-A, VEGF-C, and VEGF-D, which inhibits angiogenesis.[1][2][3]
Route: IV
Extravasation: no information
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 prescribing information.[1]
Diseases for which it is established (work in progress)
Diseases for which it is used
Patient drug information
- Ramucirumab (Cyramza) patient drug information (Chemocare)[4]
- Ramucirumab (Cyramza) package insert[1]
- Ramucirumab (Cyramza) patient drug information (UpToDate)[5]
History of changes in FDA indication
Colorectal cancer
- 2015-04-24: Approved in combination with FOLFIRI, for the treatment of metastatic colorectal cancer with disease progression on or after prior therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine. (New disease entity; based on RAISE)
Gastric cancer
- 2014-04-21: Initial approval for the treatment of patients with advanced or metastatic, gastric or gastroesophageal junction (GEJ) adenocarcinoma with disease progression on or after prior treatment with fluoropyrimidine- or platinum- containing chemotherapy. (Based on REGARD)
- 2014-11-05: Approval and indication expanded for use in combination with paclitaxel for the treatment of patients with advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma. (Requirement for prior lines of treatment removed; based on RAINBOW)
Hepatocellular carcinoma
- 2019-05-10: Approved as a single agent for hepatocellular carcinoma (HCC) in patients who have an alpha fetoprotein (AFP) of at least 400 ng/mL and have been previously treated with sorafenib. (New disease entity; based on REACH-2)
Non-small cell lung cancer
- 2014-12-12: Approved for use in combination with docetaxel for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) with disease progression on or after platinum-based chemotherapy. (New disease entity; based on REVEL)
- 2020-05-29: Approved in combination with erlotinib for first-line treatment of metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) mutations. (Approval expanded to first-line setting in EGFR+ NSCLC; based on RELAY)
History of changes in EMA indication
- 2014-12-16: Initial marketing authorization as Cyramza.
History of changes in Health Canada indication
- 2015-07-16: Initial notice of compliance as a single agent for the treatment of patients with advanced or metastatic gastric cancer or gastro-esophageal junction adenocarcinoma with disease progression on or after prior platinum and fluoropyrimidine chemotherapy.
- 2015-07-16: Initial notice of compliance in combination with paclitaxel for the treatment of patients with advanced or metastatic gastric cancer or gastro-esophageal junction adenocarcinoma with disease progression on or after prior platinum and fluoropyrimidine chemotherapy.
History of changes in PMDA indication
- 2015-03-26: Initial approval for the treatment of unresectable advanced or recurrent gastric cancer.
- 2016-05-23: New additional indication and a new dosage for the treatment of unresectable advanced or recurrent colorectal cancer.
- 2016-06-20: New additional indication and a new dosage for the treatment of unresectable advanced/relapsed non-small cell lung cancer.
- 2019-06-18: New indication for the treatment of patients with unresectable hepatocellular carcinoma whose serum AFP level is greater than 400 ng/mL and conditions have progressed after cancer chemotherapy.
Also known as
- Code names: IMC-1121B, LY-3009806
- Brand name: Cyramza
References
- Drugs
- Intravenous medications
- Mutation-specific medications
- Protein expression-specific medications
- Anti-VEGFR antibodies
- VEGFR inhibitors
- Colorectal cancer medications
- Esophageal adenocarcinoma medications
- Gastric cancer medications
- Hepatocellular carcinoma medications
- Non-small cell lung cancer medications
- Urothelial carcinoma medications
- EMA approved in 2014
- FDA approved in 2014
- Health Canada approved in 2015
- PMDA approved in 2015