Experimental and Clinical Pharmacology
New drugs for colorectal cancer - mechanisms of action
- Laurent P. Rivory, Clinical Senior Lecturer
- Aust Prescr 2002;25:108-10
- 1 October 2002
- DOI: 10.18773/austprescr.2002.110
Several new drugs have recently been approved for the treatment of advanced colorectal cancer. Raltitrexed is a folate-based inhibitor of thymidylate synthase. Capecitabine is an orally active prodrug of 5-fluorouracil which undergoes some tumour selective activation. Irinotecan is the first registered topoisomerase I poison with activity against this tumour, whereas oxaliplatin is a platinum analogue. The lack of cross-resistance between these drugs has sparked preclinical and clinical studies of a multitude of combination regimens. These regimens may improve the outcomes for patients in the near future.
Colorectal cancer has long been considered as moderately resistant to chemotherapy. Previously 5-fluorouracil (5-FU) was the only proven treatment for this indication, but it has been slowly replaced by other drugs. It is hoped these newly the approved regimens will provide the building blocks for the combination chemotherapy of the future.
Anticancer drugs act by a variety of mechanisms including:
These mechanisms induce acute cell death (necrosis), programmed cell death (apoptosis), growth arrest or differentiation. Many anticancer drugs have multiple actions on the cell. For example, 5-FU is activated to 5-fluorodeoxyuridylate (also known as fluorodeoxyuridine monophosphate), which in the presence of a reduced folate co-factor inhibits the enzyme thymidylate synthase. This blocks the production of thymidine phosphate which is required for DNA synthesis. The 5-fluorodeoxyuridylate may also be fraudulently incorporated into DNA causing a form of DNA damage.
(See Table 1)
Natural folates are vital co-factors for many cellular enzymes, specifically those that catalyse one carbon transfer reactions. Thymidylate synthase is a critical enzyme in the synthesis of the thymidine nucleotides required for DNA synthesis. This enzyme requires a reduced folate co-factor, 5-10-methylene tetrahydrofolate, to act as a carbon donor for the synthesis of thymidylate from deoxyuridylate. Raltitrexed has been specifically developed as a potent mimic of 5-10-methylene tetrahydrofolate and therefore inhibits thymidylate synthase. Many antifolate drugs are polyglutamated within cells. These polyglutamate forms are retained in the cells and, in the case of raltitrexed, this increases its potency and selectivity against thymidylate synthase.
5-FU was until recently the only drug used extensively for advanced colorectal cancer in Australia (usually in combination with leucovorin). There is now some evidence to suggest that 5-FU is most active when given by prolonged intravenous infusion. This is not very convenient for patients because it requires protracted venous access and infusion devices. Oral treatment is not a viable alternative because the absorption of 5-FU from the gastrointestinal tract is low and unpredictable. This problem has led to the development of orally bioavailable 5-FU prodrugs, such as capecitabine.
Oral capecitabine undergoes sequential hydrolysis and deamination reactions in the liver to produce 5'-deoxy-5 fluorouridine. This is converted to 5-FU by thymidine phosphorylase (also known as platelet-derived growth factor). As this enzyme is abundant in tumour tissue there is some tumour specificity in the patient's exposure to 5-FU.
The adverse effects of treatment resemble those of 5-FU when given by protracted infusion. Hand and foot syndrome (plantar-palmar erythroderma) occurs commonly, the mechanism of which is unknown.
Other oral 5-FU prodrugs (e.g. S-1, UFT) have been the subject of extensive clinical trials, particularly in Japan. These are mostly combinations of 5-FU prodrugs with uracil, which is an inhibitor of dihydropyrimidine dehydrogenase, a ubiquitous enzyme that rapidly degrades 5-FU. This results in higher and more sustained concentrations of 5-FU in the tumour tissue. Surprisingly, these drugs do not appear to produce hand and foot syndrome to the same extent as capecitabine.
|Drug||Mechanism of action|
|5-fluorouracil||Inhibition of thymidylate synthase (potentiated by addition of leucovorin)
Incorporation of fraudulent bases into DNA and RNA
|Raltitrexed||Direct inhibitor of thymidylate synthase|
|Capecitabine||As for 5-fluorouracil|
|Irinotecan||Topoisomerase I poison|
|Oxaliplatin||Bifunctional platinum alkylator of DNA|
Irinotecan is a water-soluble camptothecin analogue. Camptothecin was first isolated in extracts of the Chinese Happy Tree (Camptotheca acuminata) in the 1960s, but the mechanism of action and the anticancer potential have only recently been recognised.
Camptothecins function by 'poisoning' a nuclear enzyme, topoisomerase I. Topoisomerase I acts as a 'swivelase' in the cell, relieving topological problems (hence the name) that arise from the torsional strain that is introduced into long strands of DNA during processing (e.g. replication). This enzyme normally introduces a transient nick into one of the two strands of the DNA, which enables strand rotation and relief of the torsional strain. In the presence of camptothecins, the nick is stabilised which is equivalent to a single-strand DNA break (Fig. 1). Collision with a replication fork during DNA replication then leads to the formation of a potentially lethal double-stranded break. These breaks occur at concentrations of camptothecins that are usually much lower than those that inhibit topoisomerase I-mediated DNA relaxation. This is why these drugs are termed poisons and not inhibitors.
The anticancer activity of doxorubicin, mitozantrone, etoposide and amsacrine is partly mediated by a similar action on DNA. These drugs, however, act on topoisomerase II.
Irinotecan is a prodrug and requires activation to the metabolite SN-38. This metabolite is then conjugated in the liver to an inactive glucuronide by the enzyme UDP glucuronosyl transferase 1A1. The activity of this enzyme is deficient in people with Gilbert's disease. It is relatively common (1 in 5) and those individuals so affected have greatly reduced capacity for conjugation of SN-38 so they have an increased risk of severe toxicity when treated with irinotecan. Although Gilbert's disease is not a specific contraindication for irinotecan, affected patients should be treated with great caution.
Irinotecan is also an inhibitor of acetylcholinesterase and patients may experience an acute onset of cholinergic-like symptoms including lacrimation, sweating, abdominal cramping and diarrhoea during or within minutes of the end of infusion. The acute diarrhoea should not be confused with a delayed diarrhoea which can arise 3-10 days after treatment.
Oxaliplatin is a diaminocyclohexane platinum derivative with a broad spectrum of activity which includes colorectal cancer. It undergoes rapid non-enzymatic activation with the displacement of the oxalate ring by two chlorines and subsequent formation of a variety of aquated species. These species react with macromolecules within the cell (Fig. 2). Specifically, the bis-aquated diaminocyclohexane platinum is a bifunctional alkylator capable of reacting with adjacent guanine residues in DNA. This provides either intra- or inter-strand DNA cross-links, which interfere with DNA processing. The lack of cross-resistance with cisplatin in tumour cell models may be due to the retained bulky diaminocyclohexane side chain which projects into the minor groove of the DNA (when intrastrand cross-links are present). This may sterically inhibit the nucleotide excision and mis-match repair machinery that normally removes such adducts.
Treatment with oxaliplatin may lead to a neurotoxicity that is distinct from that caused by cisplatin. There is a transient peripheral neuropathy (paraesthesia and dysaesthesia) of the extremities and perioral regions which can be triggered or aggravated by exposure to cold. New research has suggested that chelation of intracellular calcium by the oxalic acid released during the activation of oxaliplatin may play a role in this unusual adverse effect.
The lack of cross-resistance between the thymidylate synthase inhibitors (5-FU, capecitabine, raltitrexed), oxaliplatin and irinotecan means that they could potentially be combined. Indeed, the clinical data gathered so far indicate a definite role for combination regimens in the treatment of advanced colorectal cancer. Oxaliplatin, for example, is only registered for use in combination with 5-FU and leucovorin.
Recently, several conventional cytotoxic drugs have been registered for use in the management of advanced colorectal cancer. These drugs do not represent a revolution in the treatment of this disease, but they target novel processes (irinotecan), are less prone to deactivation (oxaliplatin), are more selective (raltitrexed) or enable oral therapy (capecitabine). Combining these drugs has additive or synergistic effects in cell culture. These combinations, because of their largely non-overlapping toxicities, are being studied in clinical trials of advanced disease and post-surgical adjuvant treatment.
E-mail: [email protected]
Gunasekara NS, Faulds D. Raltitrexed. A review of its pharmacological properties and clinical efficacy in the management of advanced colorectal cancer [review]. Drugs 1998;55:423-35.
Ishikawa T, Utoh M, Sawada N, Nishida M, Fukase Y, Sekiguchi F, et al. Tumor selective delivery of 5-fluorouracil by capecitabine, a new oral fluoropyrimidine carbamate, in human cancer xenografts. Biochem Pharmacol 1998;55:1091-7.
Misset JL, Bleiberg H, Sutherland W, Bekradda M, Cvitkovic E. Oxaliplatin clinical activity: a review. Crit Rev Oncol Hematol 2000;35:75-93.
Rivory LP, Robert J. Molecular, cellular, and clinical aspects of the pharmacology of 20(S)camptothecin and its derivatives [review]. Pharmacol Ther 1995;68:269-96.
Conflict of interest: none declared
The following statements are either true or false.
1. Capecitabine enables cancer cells to be exposed to 5-fluorouracil without the need for prolonged intravenous infusion
2. Patients may be more prone to the adverse effects of oxaliplatin in cold weather.
Answers to self-test questions
Senior Scientist, Medical Oncology, Sydney Cancer Centre
Department of Pharmacology, University of Sydney, Sydney