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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.

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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.
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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

Neurological toxicity of long-term (>1 yr) thalidomide therapy in patients with multiple myeloma.

TL;DR: The results suggest that long‐term thalidomide therapy in MM may be hampered by the remarkable neurotoxicity of the drug, and that a neurological evaluation should be mandatory prior to thalidmide treatment, in order to identify patients at risk of developing a peripheral neuropathy.
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Chemotherapy-induced peripheral neurotoxicity in the era of pharmacogenomics

TL;DR: Development of advanced and high-throughput methods to study variability in human genes means pharmacogenomic analysis not only to predict response to treatment but also to assess the toxic action of drugs on normal cells (so-called toxicogenomics).
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Overall survival benefit for weekly vs. three-weekly taxanes regimens in advanced breast cancer: A meta-analysis.

TL;DR: The use of weekly paclitaxel regimens is recommended for the treatment of locally advanced/metastatic breast cancer and the observed survival benefit does not seem to stem from an increased potency of the drug with weekly regimens.
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Phase 3 study comparing the use of docetaxel on an every-3-week versus weekly schedule in the treatment of metastatic breast cancer†

TL;DR: A comparison of the 3‐week and weekly docetaxel schedules in patients with metastatic breast cancer to determine which was safer and more efficacious.
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Cisplatin-induced peripheral neurotoxicity is dependent on total-dose intensity and single-dose intensity.

TL;DR: The results suggest that not only the total dose intensity, but also the single‐dose intensity are relevant in the onset of DDP‐induced sensory neuropathy; therefore, the use of less neurotoxic schedules may prevent or reduce sensory nerve damage.
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