Vincristine chemical structure
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Vincristine

Vincristine (OncovinĀ®) is an alkaloid from the Madagascar periwinkle (Catharanthus roseus, formerly Vinca rosea and hence its name). It is used in chemotherapy. more...

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Mode of action

Tubulin is a structural protein which polymerises to form microtubules. The cell cytoskeleton and mitotic spindle, amongst other things, are made of microtubules. Vincristine binds to tubulin dimers causing disassembly of microtubule structures. Disruption of the microtubules arrests mitosis in metaphase. The vinca alkaloids therefore affect all rapidly dividing cell types, including cancer cells but also as intestinal epithelium and bone marrow.

Side effects

The main side-effects of vincristine are peripheral neuropathy and constipation. The latter may require laxatives, while the former can be a reason to reduce the dose of vincristine.

Accidental injection of vinca alkaloids into the spinal canal (intrathecal administration) is highly dangerous, with a mortality rate approaching 100%. The medical literature documents cases of ascending paralysis due to massive encephalopathy and spinal nerve demyelination, accompanied by intractable pain, almost uniformly leading to death; a handful of survivors were left with devastating neurological damage with no hope of recovery.

Uses

Vincristine, injected intravenously only, is used in various types of chemotherapy regimens. Its main uses are in non Hodgkin's lymphoma as part of the chemotherapy regimen CHOP, Hodgkin's lymphoma as part of the Stanford V chemotherapy regimen, and in acute lymphoblastic leukemia.

History

Having been used as a folk remedy for centuries, studies in the 1950s revealed that C. roseus contained 70 alkaloids, many of which biologically active. Vincristine gained FDA approval in July 1963 as Oncovin. The drug was initially marketed by Eli Lilly.

Suppliers

Three generic drug makers supply vincristine in the United States - APP, Mayne, and Sicor.

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Safety and efficacy of topical quinolones
From Ear, Nose & Throat Journal, 10/1/05

Support bacteria--it's the only culture some people have.

--Bumper sticker

Introduction

Dr. Joseph E. Dohar: At the end of the day, infectious diseases are treated with antibiotics to eradicate the bacteria causing the infections. The only caveat we must consider when taking advantage of the fatal attraction between antibiotics and the bacteria that they kill is that the killing must be done safely! "Do no harm," cried Hippocrates. In this article, we examine the evidence on the safety as well as the efficacy of ototopical quinolone therapies.

Ototoxicity

Dr. John Rutka: We think of ototoxicity as primarily involving the inner ear, but middle ear toxicity occurs, as well. We have become aware that not only do systemic agents cause ototoxicity, but topical agents are also implicated (table 1).

If we were to stop using aminoglycosides and cytotoxic agents, we would probably eliminate much of the ototoxicity that occurs in the Western world. However, we have recently learned that many other compounds are ototoxic, as well, depending on the clinical situation (table 2).

For example, the macrolide antibiotic azithromycin can be quite toxic to the inner ear in patients who are undergoing treatment for human immunodeficiency virus (HIV) infection. Vancomycin is probably not toxic to the inner ear on its own, but when it is combined with an aminoglycoside, its effects are potentiated and it is quite possible that it will cause ototoxicity.

In 2004, a consensus panel of the American Academy of Otolaryngology-Head and Neck Surgery published its review of the efficacy and safety of topical antibiotics and made several recommendations (1):

* When possible, topical antibiotic preparations that are free of potential ototoxicity are preferable to those that do have the potential for otologic injury in patients with an open middle ear or mastoid.

* When a potentially ototoxic antibiotic is chosen, it should be used only in infected ears and it should be discontinued shortly after the infection has resolved.

* When a potentially ototoxic antibiotic drop is prescribed for a patient with an open middle ear or mastoid, the patient or parent should be warned of the risk of ototoxicity. The patient or parent should be specifically instructed to call the physician or return to the office if the patient develops: (1) dizziness or vertigo, (2) heating loss or a worsening of hearing if such an impairment was already present, or (3) tinnitus. The treating physician should consider the possibility of ototoxic injury when evaluating these new or exacerbated symptoms.

The panel added that if the tympanic membrane is known to be intact and the middle ear and mastoid are closed, the use of a potentially ototoxic preparation presents no risk of ototoxic injury.

Our role as physicians requires that we protect patients. If our treatment leads to ototoxicity, we have failed the patient, especially if it could have been prevented. Although many patients adapt well to a unilateral sensorineural hearing loss and compensate for a unilateral vestibular loss, such is not the case when bilateral ototoxicity occurs. When bilateral ototoxicity occurs as a result of ototopical therapy, the consequences can be devastating in terms of total deafness and a debilitating balance disorder.

No evidence of quinolone ototoxicity

Dr. Rutka: Systemic quinolones are associated with some significant adverse effects and drug interactions. Among the adverse effects are arthropathy and chondrotoxicity, Achilles tendon rupture in the elderly, photosensitivity, and QTc prolongation. Drug interactions include an increase in the risk of cardiac arrest when a quinolone is used with theophylline, an increase in the anticoagulation properties of warfarin, and an increase in phenytoin levels above their therapeutic range.

But are topical quinolones ototoxic? I performed an Ovid MEDLINE search using ciprofloxacin as the keyword search term, and I found almost 10,000 articles--9,916 to be precise--published from 1966 through the third week of February 2004 (table 3). I then searched for articles on diagnosis that contained deafness as a keyword, and I found 2,101 articles. But when I searched for peer-reviewed articles that contained both ciprofloxacin and deafness as keywords, I did not find a single article. In other words, there has not been a single report in the world literature in which ciprofloxacin has been implicated as a cause of deafness.

Not content with this result, I performed a more focused investigation. I searched for articles with the keywords hair cells, hearing disorders, cochlear, deafness, ototoxicity, or sensorineural hearing loss and found 43,794 articles. Only 25 of these articles included any mention of ciprofloxacin:

* 7 were reports of animal studies; only 1 included any mention of ototoxicity, and it concerned mild inner ear toxicity that had been caused by nalidixic acid, which is a ciprofloxacin precursor.

* 7 articles reported comparisons of the efficacy of systemic ciprofloxacin and aminoglycosides in humans; no case of ciprofloxacin ototoxicity was reported.

* 10 articles included the results of studies of topical ciprofloxacin, and none showed that it was ototoxic.

* 1 was a unique human study in which intratympanic ciprofloxacin drops were instilled into the middle ear space of 10 patients with an acoustic neuroma; the authors found no evidence of measurable absorption of the drug in the labyrinthine fluid, cerebrospinal fluid, or serum, which indicates that the chance of ciprofloxacin toxicity is low. (2)

Chronic suppurative otitis media (CSOM)

Dr. Rutka: In patients with CSOM, randomized controlled trials have shown that antibiotic and antiseptic treatment combined with aural toilet is better than no treatment, but aural toilet alone is not. (3) Also, topical antibiotics and antiseptics are better than systemic antibiotics. Finally, there is no significant difference in effectiveness between a topical antibiotic/antiseptic alone and a combination of a topical and systemic antibiotic.

These studies have also shown that quinolones, taken either topically or systemically, appear to be more effective than other types of antibiotics. A surprising finding is that antiseptics may be just as effective as antibiotics. Topical treatment is associated with negligible or no change in hearing.

Dr. Patrick J. Antonelli: I agree. The literature clearly shows that the ototopical quinolones are efficacious (table 4). (4-12)

References

(1.) Roland PS, Stewart MG, Hannley M, et al. Consensus panel on role of potentially ototoxic antibiotics for topical middle ear use: Introduction, methodology, and recommendations. Otolaryngol Head Neck Surg 2004;130(3 suppl):S51-6.

(2.) Becvarovski Z, Kartush JM, Bojrab DI. Intratympanic ciprofloxacin and the human labyrinthine sampling model. Laryngoscope 2002; 112:686-8.

(3.) Acuin J, SmithA, Mackenzie I. Interventions for chronic suppurative otitis media. Cochrane Database Syst Rev 2000;(2):CD000473, updated Nov. 15, 2004.

(4.) Yuen PW, Lau SK, Chau PY, et al. Ofloxacin eardrop treatment for active chronic suppurative otitis media: Prospective randomized study. Am J Otol 1994;15:670-3.

(5.) Tutkun A, Ozagar A, Koc A, et al. Treatment of chronic ear disease. Topical ciprofloxacin vs topical gentamicin. Arch Otolaryngol Head Neck Surg 1995;121:1414-16.

(6.) Tong MC, Woo JK, van Hasselt CA. A double-blind comparative study of ofioxacin otic drops versus neomycin-polymyxin B-hydrocortisone otic drops in the medical treatment of chronic suppurative otitis media. J Laryngol Otol 1996; 110:309-14.

(7.) Fradis M, BrodskyA, Ben-David J, et al. Chronic otitis media treated topically with ciprofloxacin or tobramycin. Arch Otolaryngol Head Neck Surg 1997;123:1057-60.

(8.) Miro N. Controlled multicenter study on chronic suppurative otitis media treated with topical applications of ciprofloxacin 0.2% solution in single-dose containers or combination of polymyxin B, neomycin, and hydrocortisone suspension. Otolaryngol Head Neck Surg 2000;123:617-23.

(9.) Nawasreh O, Fralhat A. Topical ciprofloxacin versus topical gentamicin for chronic otitis media. East Mediterr Health J 2001;7:2630.

(10.) Couzos S, Lea T, Mueller R, et al. Effectiveness of ototopical antibiotics for chronic suppurative otitis media in Aboriginal children: A community-based, multicentre, double-blind randomised controlled trial. Med J Aust 2003;179:185-90.

(11.) Jaya C, Job A, Mathai E, Antonisamy B. Evaluation of topical povidone-iodine in chronic suppurative otitis media. Arch Otolaryngol Head Neck Surg 2003;129:1098-1100.

(12.) Macfadyen C, Gamble C, Garner P, et al. Topical quinolone vs. antiseptic for treating chronic suppurative otitis media: A randomized controlled trial. Trop Med Int Health 2005;10:190-7.

COPYRIGHT 2005 Medquest Communications, LLC
COPYRIGHT 2006 Gale Group

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