Difference between revisions of "Sipuleucel-T (Provenge)"
m |
Warner-admin (talk | contribs) m (Text replacement - "[http://www.utdol.com/online/content/search.do UpToDate (courtesy of Lexicomp)], or" to "or") |
||
(5 intermediate revisions by 2 users not shown) | |||
Line 4: | Line 4: | ||
<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. Instead, for the most current information, please refer to your preferred pharmacopeias such as | + | 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, or the prescribing information.<ref name="insert"></ref> |
==Diseases for which it is used== | ==Diseases for which it is used== | ||
Line 11: | Line 11: | ||
==Patient drug information== | ==Patient drug information== | ||
*[http://www.provenge.com/Portals/_default/Skins/ProvengeDTC/downloads/PRV.0039.USA.18-%20Provenge%20Prescribing%20Information.pdf Sipuleucel-T (Provenge) package insert]<ref name="insert"></ref> | *[http://www.provenge.com/Portals/_default/Skins/ProvengeDTC/downloads/PRV.0039.USA.18-%20Provenge%20Prescribing%20Information.pdf Sipuleucel-T (Provenge) package insert]<ref name="insert"></ref> | ||
− | *[https://chemocare.com/ | + | *[https://chemocare.com/druginfo/provenge Sipuleucel-T (Provenge) patient drug information (Chemocare)]<ref>[https://chemocare.com/druginfo/provenge Sipuleucel-T (Provenge) patient drug information (Chemocare)]</ref> |
*[http://www.uptodate.com/contents/sipuleucel-t-patient-drug-information Sipuleucel-T (Provenge) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/sipuleucel-t-patient-drug-information Sipuleucel-T (Provenge) patient drug information (UpToDate)]</ref> | *[http://www.uptodate.com/contents/sipuleucel-t-patient-drug-information Sipuleucel-T (Provenge) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/sipuleucel-t-patient-drug-information Sipuleucel-T (Provenge) patient drug information (UpToDate)]</ref> | ||
Line 17: | Line 17: | ||
*2010-04-29: [http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm210174.htm Initial FDA approval] for the treatment of asymptomatic or minimally symptomatic metastatic castrate-resistant (hormone-refractory) [[prostate cancer]]. ''(Based on D9901 and IMPACT<sub>prostate</sub>)'' | *2010-04-29: [http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm210174.htm Initial FDA approval] for the treatment of asymptomatic or minimally symptomatic metastatic castrate-resistant (hormone-refractory) [[prostate cancer]]. ''(Based on D9901 and IMPACT<sub>prostate</sub>)'' | ||
==History of changes in EMA indication== | ==History of changes in EMA indication== | ||
− | *2013-09-06: Initial authorization for treating men with asymptomatic or minimally symptomatic metastatic (non-visceral) castrate-resistant prostate cancer in whom chemotherapy is not yet clinically indicated. | + | *2013-09-06: Initial authorization for treating men with asymptomatic or minimally symptomatic metastatic (non-visceral) castrate-resistant [[prostate cancer]] in whom chemotherapy is not yet clinically indicated. |
*2015-05-06: Authorization withdrawn at the request of the manufacturer, for commercial reasons | *2015-05-06: Authorization withdrawn at the request of the manufacturer, for commercial reasons | ||
+ | |||
==Also known as== | ==Also known as== | ||
− | *'''Code name:''' | + | *'''Code name:''' APC-8015 |
*'''Brand name:''' Provenge | *'''Brand name:''' Provenge | ||
Latest revision as of 00:06, 6 July 2024
General information
Class/mechanism: Autologous cellular immunotherapy, with each dose containing a minimum of 50 million autologous CD54+ cells activated with PAP-GM-CSF. Autologous peripheral blood mononuclear cells, which include antigen presenting cells (APCs), are obtained via leukapheresis. They are then activated in vitro with prostatic acid phosphatase (PAP), an antigen expressed in prostate cancer tissue, linked to granulocyte-macrophage colony-stimulating factor (GM-CSF), and reinfused into the patient. The reinfused cells are then hypothesized to mediate immune reactions against prostate cancer cells.[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, or the prescribing information.[1]
Diseases for which it is used
Patient drug information
- Sipuleucel-T (Provenge) package insert[1]
- Sipuleucel-T (Provenge) patient drug information (Chemocare)[4]
- Sipuleucel-T (Provenge) patient drug information (UpToDate)[5]
History of changes in FDA indication
- 2010-04-29: Initial FDA approval for the treatment of asymptomatic or minimally symptomatic metastatic castrate-resistant (hormone-refractory) prostate cancer. (Based on D9901 and IMPACTprostate)
History of changes in EMA indication
- 2013-09-06: Initial authorization for treating men with asymptomatic or minimally symptomatic metastatic (non-visceral) castrate-resistant prostate cancer in whom chemotherapy is not yet clinically indicated.
- 2015-05-06: Authorization withdrawn at the request of the manufacturer, for commercial reasons
Also known as
- Code name: APC-8015
- Brand name: Provenge