Irinotecan

Drugbox
IUPAC_name = ("S")-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-
3,14-dioxo1"H"-pyrano [3’,4’:6,7] -indolizino [1,2-b] quinolin-
9-yl- [1,4’bipiperidine] -1’-carboxylate

---

width = 240
CAS_number=100286-90-6
ATC_prefix=L01
ATC_suffix=XX19
PubChem=3750
DrugBank=APRD00579
C = 33 |H = 38 |N = 4 |O = 6
molecular_weight = 586.678 g/mol
677.185 g/mol (hydrochloride)
bioavailability= NA
metabolism = Hepatic glucuronidation
elimination_half-life= 6 to 12 hours
excretion = Biliary and renal
pregnancy_category = D (Au, U.S.)
legal_status = POM (UK), ℞-only (U.S.)
routes_of_administration= Intravenous

Irinotecan is a chemotherapy agent that is a topoisomerase 1 inhibitor. Chemically, it is a semisynthetic analogue of the natural alkaloid camptothecin.

Its main use is in colon cancer, particularly in combination with other chemotherapy agents. This includes the regimen FOLFIRI which consists of infusional 5-fluorouracil, leucovorin, and irinotecan.

Irinotecan was first introduced in Japan by the Pharmaceutical arm of Yakult Honsha as Campto. In 1994, it received accelerated FDA approval in the United States, where it is now marketed by Pfizer as Camptosar. It is also known as CPT-11.

Mechanism

Irinotecan is activated by hydrolysis to SN-38, an inhibitor of topoisomerase I. This is then inactivated by glucuronidation by uridine diphosphate glucoronosyltransferase 1A1 (UGT1A1). The inhibition of topoisomerase I by the active metabolite SN-38 eventually leads to inhibition of both DNA replication and transcription.

ide effects

The most significant adverse effects of irinotecan are severe diarrhea and extreme suppression of the immune system.

Diarrhea

Irinotecan-associated diarrhea is severe and clinically significant, sometimes leading to severe dehydration requiring hospitalization or intensive care unit admission. This side effect is managed with the aggressive use of antidiarrheals such as loperamide or Lomotil with the first loose bowel movement.

Immunosuppression

The immune system is adversely impacted by irinotecan. This is reflected in dramatically lowered white blood cell counts in the blood, in particular the neutrophils. While the bone marrow, where neutrophils are made, cranks up production to compensate, the patient may experience a period of neutropenia, that is, a clinical lack of neutrophils in the blood.

Pharmacogenomics

Irinotecan is converted by an enzyme into its active metabolite SN-38, which is in turn inactivated by the enzyme UGT1A1 by glucuronidation.

People with variants of the UGT1A1 called TA₇, also known as the *28 variant, express fewer UGT1A1 enzymes in their liver often suffering from Gilbert's syndrome. During chemotherapy, these patients effectively receive a larger than expected dose because their bodies are not able to clear irinotecan as fast as others. In studies this corresponds to higher incidences of severe diarrhea and neutropenia [ Journal of Clinical Oncology, Vol 22, No 8 April 15, 2004: pp. 1382–1388] .

In 2004, a clinical study was performed that both validated prospectively the association of the *28 variant with greater toxicity and the ability of genetic testing in predicting that toxicity before chemotherapy administrationcite journal
url=http://www.jco.org/cgi/content/abstract/22/8/1382
author=Innocenti F et al
journal=Journal of Clinical Oncology
title=Genetic Variants in the UDP-glucuronosyltransferase 1A1 Gene Predict the Risk of Severe Neutropenia of Irinotecan
year = 2004
month = Apr
volume = 22
issue = 8
pages = 1382–88
pmid = 15007088] .

In 2005, the FDA made changes to the labelling of irinotecan to add pharmacogenomics recommendations that patients with polymorphisms in UGT1A1 gene, specifically the *28 variant, should perhaps receive reduced drug doses. Irinotecan is one of the first widely-used chemotherapy agents that is dosed for each patient according to his genotypecite journal
url=http://www.jco.org/cgi/content/full/24/28/4534
author=O'Dwyer PJ, Catalano RP
journal=Journal of Clinical Oncology
title=Uridine Diphosphate Glucuronosyltransferase (UGT) 1A1 and Irinotecan: Practical Pharmacogenomics Arrives in Cancer Therapy
year = 2006
month = Oct
volume = 24
issue = 28
pages = 4534–38
pmid = 17008691] .

ee also

*Camptothecin
*Topotecan (Hycamtin)
*Pharmacogenomics

References

External links

* [http://camptosar.com/products/camptosar.aspx Pfizer website]
* [http://www.pharmgkb.org/do/serve?objId=PA2001&objCls=Pathway Irinotecan Pathway on PharmGKB]