Literature DB >> 24804574

Brief review: chemotherapy-induced painful peripheral neuropathy (CIPPN): current status and future directions.

Robert L Massey1, Hee Kee Kim, Salahadin Abdi.   

Abstract

PURPOSE: Chemotherapy-induced painful peripheral neuropathy (CIPPN) affects up to 90% of cancer patients treated with chemotherapy agents. Despite the fact that it is relatively common, the underlying pathophysiology is still unclear and its treatment remains generic. Mechanisms of CIPPN are multifactorial, dependent on the specific chemotherapeutic agent used, and include multiple patient-related factors, including genetic factors that may predispose patients to either develop or not develop CIPPN. The purpose of this article is to review mechanisms, clinical signs and symptoms, diagnosis, treatment options, and prognosis for patients who develop CIPPN. We also offer research considerations for this complex and unpredictable phenomenon. PRINCIPAL
FINDINGS: Chemotherapeutic agents can damage the peripheral nervous system, including the nerve terminals, axons, cell body, and myelin sheath of sensory nerves. Herein, we describe some of the anatomical and functional changes that are thought to take place at various levels of the nervous system. On a clinical level, patients with CIPPN report multiple symptoms. It is essential to obtain an accurate history from the patient and to perform a thorough physical examination in order to obtain the patient's subjective perspective. Additionally, objective measurements may be needed in order to articulate clearly the effects of this complex syndrome and to ensure an accurate diagnosis, treatment, and prognosis.
CONCLUSIONS: The management of CIPPN remains a clinical challenge for pain practitioners. As more research is being carried out to elucidate its pathophysiology and therapy, the innovative use of several non-traditional categories of drugs seems promising in the management of this complex phenomenon. Studies addressing predictability and possible genetic predisposition are necessary not only for preventive measures but also for targeted treatments.

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Year:  2014        PMID: 24804574     DOI: 10.1007/s12630-014-0171-4

Source DB:  PubMed          Journal:  Can J Anaesth        ISSN: 0832-610X            Impact factor:   5.063


  13 in total

Review 1.  Basic science and clinical management of painful and non-painful chemotherapy-related neuropathy.

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2.  Clinical characteristics of patients with cancer referred for outpatient physical therapy.

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Review 3.  Role of innate immunity in chemotherapy-induced peripheral neuropathy.

Authors:  Megan L Uhelski; Yan Li; Miriam M Fonseca; E Alfonso Romero-Snadoval; Patrick M Dougherty
Journal:  Neurosci Lett       Date:  2021-05-04       Impact factor: 3.197

4.  Drug delivery systems for ovarian cancer treatment: a systematic review and meta-analysis of animal studies.

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5.  Rolipram, a Selective Phosphodiesterase 4 Inhibitor, Ameliorates Mechanical Hyperalgesia in a Rat Model of Chemotherapy-Induced Neuropathic Pain through Inhibition of Inflammatory Cytokines in the Dorsal Root Ganglion.

Authors:  Hee Kee Kim; Seon-Hee Hwang; Elizabeth Oh; Salahadin Abdi
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Review 6.  AAPT Diagnostic Criteria for Chronic Cancer Pain Conditions.

Authors:  Judith A Paice; Matt Mulvey; Michael Bennett; Patrick M Dougherty; John T Farrar; Patrick W Mantyh; Christine Miaskowski; Brian Schmidt; Thomas J Smith
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7.  Blockers of Wnt3a, Wnt10a, or β-Catenin Prevent Chemotherapy-Induced Neuropathic Pain In Vivo.

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8.  Nrf2 activation ameliorates mechanical allodynia in paclitaxel-induced neuropathic pain.

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Journal:  Int J Qual Stud Health Well-being       Date:  2021-12

10.  Circadian regulation of chemotherapy-induced peripheral neuropathic pain and the underlying transcriptomic landscape.

Authors:  Hee Kee Kim; Sun-Yeul Lee; Nobuya Koike; Eunju Kim; Marvin Wirianto; Mark J Burish; Kazuhiro Yagita; Hyun Kyoung Lee; Zheng Chen; Jin Mo Chung; Salahadin Abdi; Seung-Hee Yoo
Journal:  Sci Rep       Date:  2020-08-14       Impact factor: 4.996

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