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Cyclophosphamide

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Cyclophosphamide chemical structure
Cyclophosphamide

N,N-bis(2-chloroethyl)-1,3,2-oxazaphosphinan-2-amine 2-oxide
IUPAC name
CAS number
50-18-0
ATC code

L01AA01

PubChem
2907
DrugBank
APRD00408
Chemical formula {{{chemical_formula}}}
Molecular weight 261.086 g/mol
Bioavailability >75% (oral)
Metabolism Hepatic
Elimination half-life 3-12 hours
Excretion Renal
Pregnancy category
Legal status Rx-only
Routes of administration Oral, intravenous

Cyclophosphamide (the generic name for Endoxan, Cytoxan, Neosar, Procytox, Revimmune), also known as cytophosphane, an antineoplastic drug and is is a nitrogen mustard alkylating agent, from the oxazophorines group. It is used to treat various types of cancer and some autoimmune disorders. It is a "prodrug"; it is converted in the liver to active forms that have chemotherapeutic activity.

Psychologists have studeid its use form a number of points of view.

UsesEdit

The main use of cyclophosphamide is together with other chemotherapy agents in the treatment of lymphomas, some forms of Cancer leukemia[1] and some solid tumors. It is a chemotherapy drug that works by slowing or stopping cell growth. It also works by decreasing the immune system's response to various diseases. Its use is becoming more common in autoimmune diseases where disease-modifying antirheumatic drugs (DMARDs) have been ineffective. Systemic lupus erythematosus (SLE) with severe lupus nephritis, for example, may respond to pulsed cyclophosphamide. In 2005, however, standard treatment for lupus nephritis changed to mycophenolic acid (MMF) from cyclophosphamide.

Cyclophosphamide is also used to treat Minimal Change Disease and rheumatoid arthritis. It is still used for Wegener's granulomatosis, with trade name Cytoxan. For multiple sclerosis the trade name is Revimmune.

Pharmacokinetics/PharmacodynamicsEdit

Cyclophosphamide is converted by mixed function oxidase enzymes in the liver to active metabolites. The main active metabolite is 4-hydroxycyclophosphamide, which exists in equilibrium with its tautomer, aldophosphamide. Most of the aldophosphamide is oxidised by the enzyme aldehyde dehydrogenase (ALDH) to make carboxyphosphamide. A small proportion of aldophosphamide is converted into phosphoramide mustard and acrolein. Acrolein is toxic to the bladder epithelium and can lead to hemorrhagic cystitis. This can be prevented through the use of aggressive hydration and/or Mesna.

Recent clinical studies have shown that cyclophosphamide induce beneficial immunomodulatory effects in the context of adoptive immunotherapy. Although the mechanisms underlying these effects are not fully understood, several mechanisms have been suggested based on potential modulation of the host environment, including[How to reference and link to summary or text]:

  1. Elimination of T regulatory cells (CD4+CD25+ T cells) in naive and tumor-bearing hosts
  2. Induction of T cell growth factors such as type I IFNs, and/or
  3. Enhanced grafting of adoptively transferred tumor-reactive effector T cells by the creation of an immunologic space niche.

Thus, cyclophosphamide pre-conditioning of recipient hosts (for donor T cells) has been used to enhance immunity in naïve hosts, and to enhance adoptive T cell immunotherapy regimens as well as active vaccination strategies, inducing objective anti-tumor immunity.

Mode of actionEdit

The main effect of cyclophosphamide is due to its metabolite phosphoramide mustard. This metabolite is only formed in cells which have low levels of ALDH.

Phosphoramide mustard forms DNA crosslinks between (interstrand crosslinkages) and within (intrastrand crosslinkages) DNA strands at guanine N-7 positions. This leads to cell death.

Cyclophosphamide has relatively little typical chemotherapy toxicity as ALDHs are present in relatively large concentrations in bone marrow stem cells, liver and intestinal epithelium. ALDHs protect these actively proliferating tissues against toxic effects phosphoramide mustard and acrolein by converting aldophosphamide to carboxyphosphamide that does not give rise to the toxic metabolites (phosphoramide mustard and acrolein).

Side-effectsEdit

Many people taking cyclophosphamide do not have serious side effects. Side-effects include chemotherapy-induced nausea and vomiting (CINV), bone marrow suppression, stomach ache, diarrhea, darkening of the skin/nails, alopecia (hair loss) or thinning of hair, changes in color and texture of the hair, and lethargy. Hemorrhagic cystitis is a frequent complication, but this is prevented by adequate fluid intake and Mesna (sodium 2-mercaptoethane sulfonate). Mesna is a sulfhydryl donor and binds acrolein.

Cyclophosphamide is itself carcinogenic, potentially causing transitional cell carcinoma of the bladder as a long-term complication. It can lower the body's ability to fight an infection. It can cause temporary or (rarely) permanent sterility. Although it is used to treat cancer, it may increase the risk of developing another form of cancer, sometimes months to years after treatment.

Other (serious) side effects include:

  • pink/bloody urine,
  • unusual decrease in the amount of urine,
  • mouth sores,
  • unusual tiredness or weakness,
  • joint pain,
  • easy bruising/bleeding,
  • stopping of menstrual periods,
  • infertility
  • existing wounds that are slow healing.

HistoryEdit

Cyclophosphamide and the related nitrogen mustard-derived alkylating agent ifosfamide were developed by Norbert Brock and ASTA (now Baxter Oncology). Brock and his team synthesised and screened more than 1,000 candidate oxazaphosphorine compounds.[2] They converted the base nitrogen mustard into a non-toxic "transport form". This transport form was a pro-drug, subsequently actively transported into the cancer cells. Once in the cells, the pro-drug was enzymatically converted into the active, toxic form. The first clinical trials were published at the end of the 1950s.[3][4][5]

ReferencesEdit

  1. Shanafelt TD, Lin T, Geyer SM, et al (June 2007). Pentostatin, cyclophosphamide, and rituximab regimen in older patients with chronic lymphocytic leukemia. Cancer 109 (11): 2291–8.
  2. Brock N (1996). The history of the oxazaphosphorine cytostatics. Cancer 78 (3): 542–7.
  3. Wilmanns, H. (1958). {{{title}}}. Asta-Forschung und Therapie.
  4. Gross, R., and Wulf, G. (1959). Klinische und experimentelle Erfahrungen mit zyk lischen und nichtzyklischen Phosphamidestern des N-Losl in der Chemotherapie von Tumoren. Strahlentherapie 41 (Sonderband III): 361–367.
  5. Brock N (1989). Oxazaphosphorine cytostatics: past-present-future. Seventh Cain Memorial Award lecture. Cancer Res. 49 (1): 1–7.


References of psychological interestEdit

  • Adams, P. M., Fabricant, J. D., & Legator, M. S. (1982). Active avoidance behavior in the F-sub-1 progeny of male rats exposed to cyclophosphamide prior to fertilization: Neurobehavioral Toxicology & Teratology Vol 4(5) Sep-Oct 1982, 531-534.
  • Auroux, M., & Dulioust, E. (1985). Cyclophosphamide in the male rat: Behavioral effects in the adult offspring: Behavioural Brain Research Vol 16(1) Jul 1985, 25-36.
  • Bovbjerg, D., Kim, Y. T., Siskind, G. W., & Weksler, M. E. (1987). Conditioned suppression of plaque-forming cell responses with cyclophosphamide: The role of taste aversion: Annals of the New York Academy of Sciences Vol 496 May 1987, 588-594.
  • Grota, L. J., Schachtman, T. R., Moynihan, J. A., Cohen, N., & et al. (1989). Voluntary consumption of cyclophosphamide by Mrl mice: Brain, Behavior, and Immunity Vol 3(3) Sep 1989, 263-273.
  • Klosterhalfen, S., & Klosterhalfen, W. (1987). Classically conditioned effects of cyclophosphamide on white blood cell counts in rats: Annals of the New York Academy of Sciences Vol 496 May 1987, 569-577.
  • Landauer, M. R., Balster, R. L., & Harris, L. S. (1985). Attenuation of cyclophosphamide-induced taste aversions in mice by prochlorperazine, !D-9-tetrahydrocannabinol, nabilone and levonantradol: Pharmacology, Biochemistry and Behavior Vol 23(2) Aug 1985, 259-266.
  • Lin, W., Robbins, M., Wei, X., & Li, B. (1997). Dose response comparisons of cyclophosphamide in behavioral and immunological conditioning: Acta Psychologica Sinica Vol 29(Suppl) 1997, 106-109.
  • MacQueen, G. M., Siegel, S., & Landry, J. O. (1990). Acquisition and extinction of conditional immunoenhancement following training with cyclophosphamide: Psychobiology Vol 18(3) Sep 1990, 287-292.
  • O'Reilly, C. A., & Exon, J. H. (1986). Cyclophosphamide-conditioned suppression of the natural killer cell response in rats: Physiology & Behavior Vol 37(5) 1986, 759-764.
  • Patti, F., Cataldi, M. L., Nicoletti, F., Reggio, E., Nicoletti, A., & Reggio, A. (2001). Combination of cyclophosphamide and interferon-beta halts progression in patients with rapidly transitional multiple sclerosis: Journal of Neurology, Neurosurgery & Psychiatry Vol 71(3) Sep 2001, 404-407.
  • Zorzet, S., Perissin, L., Rapozzi, V., & Giraldi, T. (1998). Restraint stress reduces the antitumor efficacy of cyclophosphamide in tumor-bearing mice: Brain, Behavior, and Immunity Vol 12(1) Mar 1998, 23-33.
  • Zorzet, S., Perissin, L., Rapozzi, V., & Giraldi, T. (2002). Seasonal dependency of the effects of rotational stress and cyclophosphamide in mice bearing Lewis lung carcinoma: Brain, Behavior, and Immunity Vol 16(4) Aug 2002, 368-382.

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