Common side effects include low blood cell counts, fever, nausea, diarrhea, loss of appetite, cough, and rash.[3] Other severe side effects include allergic reactions and increased risk of infection.[3] Use in pregnancy is known to harm the baby.[3] Bendamustine is in the alkylating agents family of medication.[3] It works by interfering with the function of DNA and RNA.[3]
One combination for stage III/IV relapsed or refractory indolent lymphomas and mantle cell lymphoma (MCL), with or without prior rituximab-containing chemoimmunotherapy treatment, is bendamustine with mitoxantrone and rituximab.[7] In Germany in 2012 it has become the first line treatment of choice for indolent lymphoma.[8] After trial results released in June 2012 showed that it more than doubled disease progression-free survival when given along with rituximab. The combination also left patients with fewer side effects than the older R-CHOP treatment.[9]
Adverse effects
Common adverse reactions are typical for the class of nitrogen mustards, and include nausea, fatigue, vomiting, diarrhea, fever, constipation, loss of appetite, cough, headache, unintentional weight loss, difficulty breathing, rashes, and stomatitis, as well as immunosuppression, anemia, and low platelet counts.
Notably, this drug has a low incidence of hair loss (alopecia) unlike most other chemotherapy drugs.[10]
Pharmacology
Bendamustine is a white, water-soluble microcrystalline powder with amphoteric properties. It acts as an alkylating agent causing intra-strand and inter-strand cross-links between DNA bases.
After intravenous infusion it is extensively metabolised in the liver by cytochrome p450. More than 95% of the drug is bound to protein – primarily albumin. Only free bendamustine is active. Elimination is biphasic with a half-life of 6–10 minutes and a terminal half-life of approximately 30 minutes. It is eliminated primarily through the kidneys.
Bendamustine received its first marketing approval in Germany, where it is marketed under the tradename Ribomustin, by Astellas Pharma GmbH's licensee, Mundipharma International Corporation Limited. It is indicated as a single-agent or in combination with other anti-cancer agents for indolent non-Hodgkin's lymphoma, multiple myeloma, and chronic lymphocytic leukemia. SymBio Pharmaceuticals Ltd. holds exclusive rights to develop and market bendamustine HCl in Japan and selected Asia Pacific Rim countries.
In March 2008, Cephalon received approval from the United StatesFood and Drug Administration to market bendamustine in the US, where it is sold under the tradename Treanda, for treatment of chronic lymphocytic leukemia.[12]
In October 2008, the FDA granted further approval to market Treanda for the treatment of indolent B-cell non-Hodgkin's lymphoma that has progressed during or within six months of treatment with rituximab or a rituximab-containing regimen.[13]
Research
It is also being studied for the treatment of sarcoma.[14] It is also being investigated in phase II trials for the non-cancer treatment of AL amyloidosis.[15]
^British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. p. 579. ISBN9780857111562.
^World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
^World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.
^Weide R, Hess G, Köppler H, Heymanns J, Thomalla J, Aldaoud A, et al. (July 2007). "High anti-lymphoma activity of bendamustine/mitoxantrone/rituximab in rituximab pretreated relapsed or refractory indolent lymphomas and mantle cell lymphomas. A multicenter phase II study of the German Low Grade Lymphoma Study Group (GLSG)". Leukemia & Lymphoma. 48 (7): 1299–1306. doi:10.1080/10428190701361828. PMID17613757. S2CID2381354.
^Ozegowski W, Krebs D (June 1963). "Aminosäureantagonisten. III. ω-[Bis-(β-chloräthyl)-amino-benzimidazolyl-(2)]-propion- bzw. -buttersäuren als potentielle Cytostatika". Advanced Synthesis and Catalysis. 20 (3–4): 178–186. doi:10.1002/prac.19630200310.
^Lagos GG, Lentzsch S, Comenzo RL, Zonder JA, Osman K, Gould J, et al. (8 December 2017). "Long Term Follow up of Patients with Relapsed/Refractory Systemic Light Chain (AL) Amyloidosis Treated with Bendamustine and Dexamethasone in a Phase 2 Study". Blood. 130 (supplement 1): 1838.