Please cite this article in press as: Pizzamiglio C, et al. Nerve conduction, circulating osteopontin and
taxane-induced neuropathy in breast cancer patients. Neurophysiologie Clinique/Clinical Neurophysiology (2019),
https://doi.org/10.1016/j.neucli.2019.12.001
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ORIGINAL ARTICLE
Nerve conduction, circulating osteopontin
and taxane-induced neuropathy in breast
cancer patients
Chiara Pizzamiglio
a,1
, Paolo Ripellino
b,1
, Paolo Prandi
c
,
Nausicaa Clemente
d
, Chiara Saggia
e
, Valentina Rossi
e
,
Gionata Strigaro
a,c,*
, Pier Luigi Foglio Bonda
f
,
Cristoforo Comi
a,1
, Roberto Cantello
a,c,1
a
Department of Translational Medicine, Section of Neurology, University of Piemonte-Orientale, Via
Solaroli 17, 28100 Novara, Italy
b
Department of Neurology, Neurocenter of Southern-Switzerland, Via Tesserete 46, 6900 Lugano,
Switzerland
c
Department of Neurology, ‘‘Maggiore della Carità’’ University Hospital, Corso-Mazzini 18, 28100 Novara,
Italy
d
Department of Health Sciences, University of Piemonte Orientale, Via Solaroli 17, 28100 Novara, Italy
e
Medical Oncology, ‘‘Maggiore della Carità’’ University Hospital, Corso-Mazzini 18, 28100 Novara, Italy
f
Department of Translational Medicine, University of Piemonte Orientale, Via Solaroli 17, 28100 Novara,
Italy
Received 22 July 2019; accepted 9 December 2019
KEYWORDS
Polyneuropathy;
Taxanes;
Nerve conduction
studies;
Osteopontin;
Breast cancer
Summary
Objective. — Chemotherapy-induced peripheral neuropathy (CIPN) is a disabling complication
related to taxanes. Underlying mechanisms are not completely understood and no specific
treatment exists. We investigated the role of nerve conduction studies (NCS) and of serum
osteopontin (OPN) measurement as a means to stratify the risk of developing taxane-induced
neuropathy (TIN).
Methods. — We enrolled 50 women with breast cancer treated with taxanes (docetaxel or pacli-
taxel) in a 3-month prospective study. They were evaluated before chemotherapy (time-point
T0) and followed up at 1 (T1) and 3 (T2) months with clinical examinations/scales, quality of
life (QoL) questionnaires, NCS, and serum OPN dosages.
Results. — A reduction of sural and superficial peroneal sensory action potentials was seen
at T1, with a progression at T2 (P < 0.001). In contrast, a significant impact of neu-
ropathic symptoms on QoL only occurred at T2 (P < 0.01). OPN levels at T0 inversely
correlated to axonal loss in the sural nerve (T0—T2, P < 0.01). OPN levels at T0 were
∗
Corresponding author.
E-mail address: gionata.strigaro@gmail.com (G. Strigaro).
1
These authors contributed equally to the present research.
https://doi.org/10.1016/j.neucli.2019.12.001
0987-7053/© 2019 Elsevier Masson SAS. All rights reserved.