Literature DB >> 12576935

Severe toxicity related to the 5-fluorouracil/leucovorin combination (the Mayo Clinic regimen): a prospective study in colorectal cancer patients.

Medy Tsalic1, Gil Bar-Sela, Alex Beny, Bella Visel, Nissim Haim.   

Abstract

The Mayo Clinic regimen of leucovorin 20 mg/m followed immediately by 5-fluorouracil 425 mg/m administered for 5 consecutive days every 4 weeks is commonly used in the treatment of colorectal cancer. This study was aimed at prospectively determining the incidence and pattern of severe toxicity associated with this regimen. We evaluated prospectively 243 patients with colorectal cancer treated in our department with the Mayo Clinic regimen for the incidence of severe toxicity (defined as toxicity requiring hospitalization). Of the 243 patients, 32 (13%) were hospitalized for chemotherapy-related toxicity. Major toxicities included neutropenic fever in 21 (9%), grade III/IV mucositis in 25 (10%) and grade III/IV diarrhea in 20 (8%). There were five (2%) treatment-related deaths. Female patients exhibited a higher incidence of severe toxicity (18%) and toxic death (4/105) than did male patients (9% and 1/138, respectively). Elderly patients (> or =70 years) had a higher incidence of severe toxicity than younger patients did (24% versus 7%, < 0.001). Toxic death occurred in 4 of 89 patients aged 70 years or more compared to 1 of 154 in younger patients. Most episodes of severe toxicity (56%) and toxic deaths (4/5) were observed after the first cycle. We conclude that the Mayo Clinic regimen can be associated with severe toxicity, usually occurring after the first cycle. Female gender and advanced age predict severe toxicity; therefore, dose reduction in high-risk patients should be considered, especially during the first cycle.

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Year:  2003        PMID: 12576935     DOI: 10.1097/01.COC.0000017526.55135.6D

Source DB:  PubMed          Journal:  Am J Clin Oncol        ISSN: 0277-3732            Impact factor:   2.339


  14 in total

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2.  Beating the odds: efficacy and toxicity of dihydropyrimidine dehydrogenase-driven adaptive dosing of 5-FU in patients with digestive cancer.

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3.  Adjuvant chemotherapy in elderly patients (>or=75 yr) completely resected for colon cancer stage III compared to younger patients: toxicity and prognosis.

Authors:  Søren Astrup Jensen; Adam Vilmar; Jens Benn Sørensen
Journal:  Med Oncol       Date:  2006       Impact factor: 3.064

4.  Prognostic factors in 165 elderly colorectal cancer patients.

Authors:  Ke-Jun Nan; Hai-Xia Qin; Guang Yang
Journal:  World J Gastroenterol       Date:  2003-10       Impact factor: 5.742

5.  Predicting 5-fluorouracil toxicity in colorectal cancer patients from peripheral blood cell telomere length: a multivariate analysis.

Authors:  M B Garg; L F Lincz; K Adler; F E Scorgie; S P Ackland; J A Sakoff
Journal:  Br J Cancer       Date:  2012-09-18       Impact factor: 7.640

6.  Risk factors for oral mucositis in paediatric oncology patients receiving alkylant chemotherapy.

Authors:  Giulia Fadda; Guglielmo Campus; PierFranca Lugliè
Journal:  BMC Oral Health       Date:  2006-10-18       Impact factor: 2.757

7.  The impact of low-grade toxicity in older people with cancer undergoing chemotherapy.

Authors:  T Kalsi; G Babic-Illman; P Fields; S Hughes; N Maisey; P Ross; Y Wang; D Harari
Journal:  Br J Cancer       Date:  2014-09-30       Impact factor: 7.640

8.  Emergency use of uridine triacetate for the prevention and treatment of life-threatening 5-fluorouracil and capecitabine toxicity.

Authors:  Wen Wee Ma; Muhammad Wasif Saif; Bassel F El-Rayes; Marwan G Fakih; Thomas H Cartwright; James A Posey; Thomas R King; Reid W von Borstel; Michael K Bamat
Journal:  Cancer       Date:  2016-09-13       Impact factor: 6.860

9.  5-FU therapeutic drug monitoring as a valuable option to reduce toxicity in patients with gastrointestinal cancer.

Authors:  Katarzyna Morawska; Françoise Goirand; Laurine Marceau; Madeline Devaux; Adèle Cueff; Aurélie Bertaut; Julie Vincent; Leila Bengrine-Lefevre; François Ghiringhelli; Antonin Schmitt
Journal:  Oncotarget       Date:  2018-01-30

10.  Xanthohumol, a Prenylated Flavonoid from Hops, Induces DNA Damages in Colorectal Cancer Cells and Sensitizes SW480 Cells to the SN38 Chemotherapeutic Agent.

Authors:  Alessandra Scagliarini; Aline Mathey; Virginie Aires; Dominique Delmas
Journal:  Cells       Date:  2020-04-10       Impact factor: 6.600

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