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Chemotherapy-induced peripheral neurotoxicity: a critical analysis.

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TLDR
This review will address the increasing importance and challenge of chemotherapy‐induced neurotoxicity, with a focus on neuropathy associated with the treatment of breast cancer, colorectal cancer, testicular cancer, and hematological cancers.
Abstract
With a 3-fold increase in the number of cancer survivors noted since the 1970s, there are now over 28 million cancer survivors worldwide. Accordingly, there is a heightened awareness of long-term toxicities and the impact on quality of life following treatment in cancer survivors. This review will address the increasing importance and challenge of chemotherapy-induced neurotoxicity, with a focus on neuropathy associated with the treatment of breast cancer, colorectal cancer, testicular cancer, and hematological cancers. An overview of the diagnosis, symptomatology, and pathophysiology of chemotherapy-induced peripheral neuropathy will be provided, with a critical analysis of assessment strategies, neuroprotective approaches, and potential treatments. The review will concentrate on neuropathy associated with taxanes, platinum compounds, vinca alkaloids, thalidomide, and bortezomib, providing clinical information specific to these chemotherapies. CA Cancer J Clin 2013;63:419-437. ©2013 American Cancer Society, Inc.

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Reactive Oxygen Species (ROS)-Based Nanomedicine.

TL;DR: In this article, the intrinsic biochemical properties of reactive oxygen species (ROS) underlie the mechanisms that regulate various physiological functions of living organisms, and they play an essential role in regulating various physiological function.
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Incidence, prevalence, and predictors of chemotherapy-induced peripheral neuropathy: A systematic review and meta-analysis.

TL;DR: A systematic review of studies reporting the prevalence of Chemotherapy‐induced peripheral neuropathy identified 31 studies with data from 4179 patients and identified a number of genetic and clinical risk factors that require further study.
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Microbiota: a key orchestrator of cancer therapy.

TL;DR: The evidence for the ability of the microbiota to modulate chemotherapy, radiotherapy and immunotherapy is discussed with a focus on the microbial species involved, their mechanism of action and the possibility of targeting the microbiome to improve anticancer efficacy while preventing toxicity.
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Mechanisms of Chemotherapy-Induced Peripheral Neuropathy.

TL;DR: A better understanding of the risk factors and underlying mechanisms of CIPN is needed to develop effective preventive and therapeutic strategies and the neurotoxicity mechanisms of the most common antineoplastic agents are reviewed.
Journal ArticleDOI

Pathophysiology of Chemotherapy-Induced Peripheral Neuropathy

TL;DR: This review focusses on the commonly used antineoplastic substances oxaliplatin, cisPlatin, vincristine, docetaxel, and paclitaxel which interfere with the cancer cell cycle—leading to cell death and tumor degradation—and cause severe acute and chronic peripheral neuropathies.
References
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Journal ArticleDOI

Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.

TL;DR: The authors performed a genome‐wide association analysis of patients with colon cancer who received oxaliplatin‐based chemotherapy to identify potential genetic markers for severe oxaliPlatin‐induced chronic peripheral neuropathy (OXCPN).
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Histology and platinum content of sensory ganglia and sural nerves in patients treated with cisplatin and carboplatin: an autopsy study.

TL;DR: The hypothesis that cisplatin neuropathy is a neuroneopathy rather than a dying‐back axonopathy is supported, at least so in liver, sensory ganglia and sural nerves.
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Erythropoietin protects sensory axons against paclitaxel-induced distal degeneration

TL;DR: In an animal model of paclitaxel-induced distal sensory polyneuropathy, recombinant human erythropoietin protects against distal axonal degeneration and this effect is associated with downregulation of detyrosinated tubulin.
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Limited Access Trial Using Amifostine for Protection Against Cisplatin- and Three-Hour Paclitaxel–Induced Neurotoxicity: A Phase II Study of the Gynecologic Oncology Group

TL;DR: Amifostine's level of activity in this trial was insufficient to warrant further study in a phase III trial, and it would appear that VPT measurements are less sensitive to the development of peripheral neuropathy than the neurotoxicity questionnaire.
Journal ArticleDOI

Follow-up psychophysical studies in bortezomib-related chemoneuropathy patients.

TL;DR: The results of this article indicate a persistent, painful peripheral neuropathy in patients treated with bortezomib and pilot data indicates a loss of nerve fibers innervating the area of pain.
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