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Abstract Details

The prevalence, severity and risk factors for chemotherapy induced peripheral neuropathy at 0 and 2 years after the completion of paclitaxel therapy
Neuromuscular and Clinical Neurophysiology (EMG)
P2 - Poster Session 2 (5:30 PM-6:30 PM)
12-012

Determine the prevalence, severity and risk factors for chemotherapy induced peripheral neuropathy (CIPN) at 0 and 2 years after the completion of paclitaxel therapy for breast cancer.

CIPN is a dose limiting side effect of neurotoxic chemotherapy which carries substantial morbidity. CIPN risk factors and natural history are poorly understood.

Retrospective chart review of breast cancer patients treated with paclitaxel monotherapy at the University of Utah between 1999 and 2015. Medical records were reviewed to determine diagnosis of CIPN and assign NCI CTCAE severity (if not documented). Risk factors analysis evaluated by ICD9/10 codes of medical problems prior to chemotherapy.

N=565, mean age 51.9(±12.25). 99.97% female, 57.7% weekly and 42.3% dose dense paclitaxel.  Mean total paclitaxel dose (mg/m2) of those with vs. those without CIPN was 753.7±231 vs. 731.5±.256.0 p=0.343. Only 11.8% of those with documented CIPN had a documented CTCAE neuropathy severity score.

 

At the conclusion of chemotherapy: 73% had CIPN: 32% grade 1, 36% grade 2, 4% grade 3, <1% grade 4 neuropathy.  At 2 years after chemotherapy: 36% had CIPN: 20% grade 1, 15% grade 2, >1% grade 3. 

 

Risk Factor Analysis: Relative risk and confidence interval at completion  and 2 years:  

type 2 diabetes 1.120(.976-1.285) and 1.323(1.056-1.658), idiopathic polyneuropathy 1.350(1.290-1.420) and 2.050(1.88-2.235), alcoholism 0.669(.0334-1.240) and 1.528 (1.015-2.301), hyperlipidemia 1.101(.966-1.256) and 1.349(1.097-1.658), chronic hep C 1.009 (.966-1.256) and 2.038(1.187-2.220), hypocalcemia 1.345(1.283-1.417) and 1.001(.338-2.704), previous neuropathy related to a drug 1.346(1.281-1.412) and 2.026(1.860-2.206), essential hypertension 1.098(.987-1.22) and 1.369(1.153-1.1622).

The prevalence of CIPN after paclitaxel therapy approaches 75% and over 1/3 of patients continue to have CIPN after 2 years. .Amongst other risk factors, the components of metabolic syndrome are associated with increased risk of persistent CIPN. More detailed prospective study is needed to better understand CIPN risk factors.

Authors/Disclosures
Noah A. Kolb, MD (University of Vermont Medical Center)
PRESENTER
Dr. Kolb has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Abalone Medical. Dr. Kolb has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Disarm Therapeutics. Dr. Kolb has received personal compensation in the range of $0-$499 for serving as a Consultant for Eisana corporation. Dr. Kolb has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Alexion Pharmaceuticals. Dr. Kolb has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for NINDS. Dr. Kolb has received personal compensation in the range of $500-$4,999 for serving as a Consultant for UCB. Dr. Kolb has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Locks Law. Dr. Kolb has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for walk up law office . Dr. Kolb has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for ralston, pope, diehl. The institution of Dr. Kolb has received research support from National Cancer Institute.
Summer Karafiath, MD (University of Utah) No disclosure on file
No disclosure on file
J. R. Singleton, MD (University of Utah Department of Neurology) Dr. Singleton has received research support from NIH.
A. Gordon Smith, MD, FAAN (VCU Health System Department of Neurology) Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Alexion. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Argenx. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Merz. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Sangamo. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for US Department of Justice. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Janssen. Dr. Smith has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Eidos. Dr. Smith has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Lexicon. Dr. Smith has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Alexion. The institution of Dr. Smith has received research support from NIH (NINDS, NIDDK). Dr. Smith has received publishing royalties from a publication relating to health care. Dr. Smith has received personal compensation in the range of $0-$499 for serving as a Study Section with NIH.