Difference between revisions of "Alemtuzumab (Campath)"
Warner-admin (talk | contribs) m (Text replacement - "Category:Intravenous chemotherapy" to "Category:Intravenous medications") |
Warner-admin (talk | contribs) m (Text replacement - "Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL)" to "Chronic lymphocytic leukemia (CLL/SLL)") |
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*[[Adult T-cell leukemia-lymphoma]] | *[[Adult T-cell leukemia-lymphoma]] | ||
*[[Autoimmune cytopenias]] | *[[Autoimmune cytopenias]] | ||
− | *[[Chronic lymphocytic leukemia (CLL | + | *[[Chronic lymphocytic leukemia (CLL/SLL)]] |
*[[Cutaneous T-cell lymphoma]] | *[[Cutaneous T-cell lymphoma]] | ||
*[[Hypereosinophilic syndrome]] | *[[Hypereosinophilic syndrome]] | ||
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
− | *5/7/2001: Initial approval "for the treatment of patients with [[Chronic lymphocytic leukemia (CLL | + | *5/7/2001: Initial approval "for the treatment of patients with [[Chronic lymphocytic leukemia (CLL/SLL) | B-cell chronic lymphocytic leukemia]] who have been treated with [[:Category:Alkylating_agents|alkylating agents]] and who have failed [[Fludarabine (Fludara) | fludarabine]] therapy."<ref>[http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2001/alemmil050701L.htm FDA approval letter dated May 7th, 2001]</ref> |
− | *9/19/2007: Indication expanded "to include use as a single agent for treatment of [[Chronic lymphocytic leukemia (CLL | + | *9/19/2007: Indication expanded "to include use as a single agent for treatment of [[Chronic lymphocytic leukemia (CLL/SLL) | B-cell chronic lymphocytic leukemia (B-CLL)]]" |
*October 2012: Genzyme withdraws drug from USA and EU (still available for B-CLL patients, however). See Lancet editorial.<ref>[http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)61776-0/fulltext Alemtuzumab for multiple sclerosis]</ref> | *October 2012: Genzyme withdraws drug from USA and EU (still available for B-CLL patients, however). See Lancet editorial.<ref>[http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)61776-0/fulltext Alemtuzumab for multiple sclerosis]</ref> | ||
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[[Category:Adult T-cell leukemia-lymphoma medications]] | [[Category:Adult T-cell leukemia-lymphoma medications]] | ||
[[Category:Autoimmune cytopenia medications]] | [[Category:Autoimmune cytopenia medications]] | ||
− | [[Category:Chronic lymphocytic leukemia (CLL | + | [[Category:Chronic lymphocytic leukemia (CLL/SLL) medications]] |
[[Category:Cutaneous T-cell lymphoma medications]] | [[Category:Cutaneous T-cell lymphoma medications]] | ||
[[Category:Hypereosinophilic syndrome medications]] | [[Category:Hypereosinophilic syndrome medications]] |
Revision as of 14:58, 14 October 2017
General information
Class/mechanism: Anti-CD52 antibody that is believed to cause antibody-dependent cell-mediated cytotoxicity of cells that express the CD52 antigen on their surface: B and T lymphocytes, most monocytes, macrophages, natural killer (NK) cells, and a subpopulation of granulocytes.[1][2][3]
Route: IV
Extravasation: neutral
- Use of alemtuzumab (Lemtrada) requires participation in the Lemtrada REMS program.
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, Medscape, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]
Diseases for which it is used
- Adult T-cell leukemia-lymphoma
- Autoimmune cytopenias
- Chronic lymphocytic leukemia (CLL/SLL)
- Cutaneous T-cell lymphoma
- Hypereosinophilic syndrome
- Myelodysplastic syndrome
- Peripheral T-cell lymphoma
- Waldenström macroglobulinemia
Patient drug information
- Alemtuzumab (Campath) patient drug information (Chemocare)[4]
- Brief patient counseling information can be found at the end of page 2 of the Alemtuzumab (Campath) package insert[1]
- Alemtuzumab (Campath) patient drug information (UpToDate)[5]
History of changes in FDA indication
- 5/7/2001: Initial approval "for the treatment of patients with B-cell chronic lymphocytic leukemia who have been treated with alkylating agents and who have failed fludarabine therapy."[6]
- 9/19/2007: Indication expanded "to include use as a single agent for treatment of B-cell chronic lymphocytic leukemia (B-CLL)"
- October 2012: Genzyme withdraws drug from USA and EU (still available for B-CLL patients, however). See Lancet editorial.[7]
Also known as
Precise Name: alemtuzumab (RXCUI 117055)
Campath, Campath-1H, Lemtrada, Mabcampath
References
- ↑ 1.0 1.1 1.2 Alemtuzumab (Campath) package insert
- ↑ Alemtuzumab (Campath) package insert (locally hosted backup)
- ↑ Campath manufacturer's website
- ↑ Alemtuzumab (Campath) patient drug information (Chemocare)
- ↑ Alemtuzumab (Campath) patient drug information (UpToDate)
- ↑ FDA approval letter dated May 7th, 2001
- ↑ Alemtuzumab for multiple sclerosis
- Drug index
- Chemotherapy
- Intravenous medications
- Neutral chemotherapy
- Immunotherapy
- Antibody medications
- Anti-CD52 antibodies
- Adult T-cell leukemia-lymphoma medications
- Autoimmune cytopenia medications
- Chronic lymphocytic leukemia (CLL/SLL) medications
- Cutaneous T-cell lymphoma medications
- Hypereosinophilic syndrome medications
- Myelodysplastic syndrome medications
- Peripheral T-cell lymphoma medications
- Waldenström macroglobulinemia medications
- REMS program
- Drugs FDA approved in 2001