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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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The experience of chemotherapy-induced peripheral neuropathy in adult cancer patients: a qualitative thematic synthesis

TL;DR: Qualitative research evidence on the experience of adult cancer patients living with chemotherapy‐induced peripheral neuropathy (CIPN) is systematically identified, appraised and synthesised, and four analytical themes emerged: CIPN is an unclear experience, a less important risk, impact on quality of life and a feature of cancer survivorship.
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Sulforaphane improves chemotherapy efficacy by targeting cancer stem cell-like properties via the miR-124/IL-6R/STAT3 axis.

TL;DR: Co-exposure of SFN and CDDP significantly inhibited the viabilities of gastric cancer cells and suggested a mechanism whereby SFN enhanced the anti-cancer functions of CDDP, which helped to regard SFN as a potential chemotherapeutic factor in Gastric cancer.
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Genetic and Modifiable Risk Factors Contributing to Cisplatin-induced Toxicities

TL;DR: In this paper, a review summarizes the current state of knowledge with regard to specific adverse sequelae following cisplatin-based therapy, with a focus on ototoxicity, neurotoxicity, nephrotoxicity, myelosuppression, and nausea/emesis.
Journal ArticleDOI

Comparative study of the effects of venlafaxine and duloxetine on chemotherapy-induced peripheral neuropathy.

TL;DR: Duloxetine seems to be more effective than venlafaxine in decreasing the symptoms of chemotherapy-induced peripheral neuropathy and neuropathic pain grade.
Journal ArticleDOI

Tumor-Specific Chemotherapy by Nanomedicine-Enabled Differential Stress Sensitization.

TL;DR: Evidence that this engineered nanosystem features largely elevated therapeutic efficacy, mitigated side effects, as well as distinct anti-metastasis function is also evidence that it may greatly benefit future nanomedicine design.
References
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World Cancer Report

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Leucovorin and Fluorouracil With or Without Oxaliplatin as First-Line Treatment in Advanced Colorectal Cancer

TL;DR: The LV5FU2-oxaliplatin combination seems beneficial as first-line therapy in advanced colorectal cancer, demonstrating a prolonged progression-free survival with acceptable tolerability and maintenance of QoL.
Journal ArticleDOI

CTCAE v3.0: development of a comprehensive grading system for the adverse effects of cancer treatment.

TL;DR: Recent progress in the evolution of adverse effects grading systems is updated and the development of CTCAE v3.0 is reviewed, which represents an international collaboration and consensus of the oncology research community.
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