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abstract:
Comorbidities and Risk of Chemotherapy-Induced Peripheral Neuropathy Among Participants 65 Years or Older in Southwest Oncology Group Clinical Trials
June 20, 2016
Background Neuropathy
is a debilitating toxicity associated with various chemotherapy agents.
We evaluated the association between common
comorbid conditions and the development of
peripheral neuropathy in patients treated with taxane-based
chemotherapy.
Methods We examined
the Southwest Oncology Group database to identify phase II and III
trials that included taxane therapy from 1999
to 2011. We linked the Southwest Oncology Group
clinical records to Medicare claims data according to Social Security
number,
sex, and date of birth. The following disease
conditions potentially associated with peripheral neuropathy were
evaluated:
diabetes, hypothyroidism, hypercholesterolemia,
hypertension, varicella zoster, peripheral vascular disease, and
autoimmune
diseases. Multivariate logistic regression was
used to model the odds of experiencing grade 2 to 4 neuropathy.
Results A total of 1,401 patients from 23 studies were included in the analysis. Patients receiving paclitaxel were more likely to
experience grade 2 to 4 neuropathy compared with docetaxel (25% v 12%). The inclusion of a platinum agent was also associated with greater neuropathy (OR, 1.68). For each increase in age of 1 year, the odds of neuropathy increased 4%. Patients with complications from diabetes had more than twice the odds of having neuropathy (OR, 2.13) compared with
patients with no diabetes. In contrast, patients with autoimmune disease
were half as likely to experience
neuropathy (OR, 0.49). The other conditions were not associated with neuropathy.
Conclusion We found
that in addition to drug-related factors, age and history of diabetes
were independent predictors of the development
of chemotherapy-induced peripheral neuropathy.
Interestingly, we also observed that a history of autoimmune disease was
associated
with reduced odds of neuropathy. Patients with
diabetic complications may choose to avoid paclitaxel or taxane plus
platinum
combination therapies if other efficacious
options exist.
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