Critically short telomeres and toxicity of chemotherapy in early breast cancer.
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Identifiers
Date
2017
Authors
Quintela-Fandino, Miguel
Soberon, Nora
Lluch, Ana
Manso, Luis
Calvo, Isabel
Cortes, Javier
Moreno-Antón, Fernando
Gil-Gil, Miguel
Martinez-Jánez, Noelia
Gonzalez-Martin, Antonio
Advisors
Journal Title
Journal ISSN
Volume Title
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Abstract
Cumulative toxicity from weekly paclitaxel (myalgia, peripheral neuropathy, fatigue) compromises long-term administration. Preclinical data suggest that the burden of critically short telomeres ( 21.9% CSTs) had 2-fold higher number of neuropathy (P = 0.04) or fatigue (P = 0.019) episodes and >3-fold higher number of myalgia episodes (P = 0.005). The average telomere length was unrelated to the incidence of side effects.The percentage of CSTs, but not the average telomere size, is associated with weekly paclitaxel-derived toxicity.
Description
MeSH Terms
Adult
Aged
Aged, 80 and over
Antineoplastic Agents
Breast Neoplasms
Chemotherapy, Adjuvant
Female
Humans
In Situ Hybridization, Fluorescence
Indoles
Middle Aged
Neoadjuvant Therapy
Paclitaxel
Telomere
Telomere Shortening
Aged
Aged, 80 and over
Antineoplastic Agents
Breast Neoplasms
Chemotherapy, Adjuvant
Female
Humans
In Situ Hybridization, Fluorescence
Indoles
Middle Aged
Neoadjuvant Therapy
Paclitaxel
Telomere
Telomere Shortening
DeCS Terms
CIE Terms
Keywords
breast cancer, critically short telomeres, telomere length, toxicity, weekly paclitaxel