Literature DB >> 2124943

Cyclophosphamide, methotrexate, and 5-fluorouracil (CMF)-induced ocular toxicity.

C L Loprinzi1, R R Love, J A Garrity, M M Ames.   

Abstract

Ocular toxicity is a common, but poorly understood, sequela from CMF chemotherapy. We investigated this toxicity in patients receiving CMF therapy. Detailed interviews in 210 patients revealed that new, unpleasant ocular symptoms developed in 42% of patients receiving CMF, in 39% of subjects receiving other regimens containing 5-fluorouracil (5-FU), and only in 18% of subjects receiving a variety of chemotherapy regimens not containing 5-FU. CMF-associated ocular symptoms usually consisted of mild to marked tearing, ocular pruritus, and/or burning. These toxicities usually began 11-17 days after starting a cycle of CMF and lasted for 10-15 days. 5-FU was detected in the tears of 12 tested patients within several minutes after intravenous 5-FU (peak concentrations as high as 60 micrograms/ml). 5-FU tear concentrations did not correlate with the presence or absence of ocular toxicity. There is no established antidote for this toxicity although some patients have reported subjective benefit from cryotherapy, applied around the period of 5-FU injections, or cromolyn sodium eye drops.

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Year:  1990        PMID: 2124943     DOI: 10.3109/07357909009012068

Source DB:  PubMed          Journal:  Cancer Invest        ISSN: 0735-7907            Impact factor:   2.176


  10 in total

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Review 2.  Supportive cryotherapy: a review from head to toe.

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4.  Predictive factors for ocular complications caused by anticancer drug S-1.

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5.  Ocular surface and tear film abnormalities in women under adjuvant chemotherapy for breast cancer with the 5-Fluorouracil, Epirubicin and Cyclophosphamide (FEC) regimen.

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Review 6.  Breast cancer medications and vision: effects of treatments for early-stage disease.

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8.  Noninvasive direct detection of ocular mucositis by in vivo confocal microscopy in patients treated with S-1.

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  10 in total

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