Pharmacological treatment of neuropathic cancer pain: a comprehensive review of the current literature.
Pain Pract. 2012 Mar;12(3):219-51.
Source
1st Anaesthesiology Clinic, Pain Relief and Palliative Care Unit, Aretaieion University Hospital, University of Athens, Greece. athinajv@ath.forthnet.grAbstract
Neuropathic
cancer pain (NCP), commonly encountered in clinical practice, may be
cancer-related, namely resulting from nervous system tumor invasion,
surgical nerve damage during tumor removal, radiation-induced nerve
damage and chemotherapy-related neuropathy, or may be of benign origin,
unrelated to cancer. A neuropathic component is evident in about 1/3 of
cancer pain cases. Although from a pathophysiological perspective NCP
may differ from chronic neuropathic pain (NP), such as noncancer-related
pain, clinical practice, and limited publications have shown that these
two pain entities may share some treatment modalities. For example,
co-analgesics have been well integrated into cancer pain-management
strategies and are often used as First-Line options for the treatment of
NCP.
These drugs, including antidepressants and anticonvulsants, are
recommended by evidence-based guidelines, whereas, others such as
lidocaine patch 5%, are supported by randomized, controlled, clinical
data and are included in guidelines for restricted conditions treatment.
The vast majority of these drugs have already been proven useful in the
management of benign NP syndromes.
Treatment decisions for patients
with NP can be difficult.
The intrinsic difficulties in performing
randomized controlled trials in cancer pain have traditionally justified
the acceptance of drugs already known to be effective in benign NP for
the management of malignant NP, despite the lack of relevant high
quality data. Interest in NCP mechanisms and pharmacotherapy has
increased, resulting in significant mechanism-based treatment advances
for the future. In this comprehensive review, we present the latest
knowledge regarding NCP pharmacological management.
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