TY - JOUR
T1 - Management of peripheral neuropathy induced by chemotherapy
AU - Fradkin, Maayan
AU - Batash, Ron
AU - Elmaleh, Shiran
AU - Debi, Ronen
AU - Schaffer, Pamela
AU - Schaffer, Moshe
AU - Asna, Noam
N1 - Publisher Copyright:
© 2019 Bentham Science Publishers.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Background: Chemotherapy-induced peripheral neuropathy (CIPN) is considered a severe side effect of therapeutic agents with limited treatment options. The incidence of CIPN in cancer patients is approximately 3–7% in cytostatic monotherapy and as high as 38% in cases of polychemotherapy. The prevalence of CIPN was found to be 68% within the first month of chemotherapy treatment. In some cases, CIPN can resolve, partially or completely, after completion of the treatment; in other cases, it can remain for a long time and affect the patient's quality of life. Objective: The aim of this study is to present up-to-date data regarding available treatment options for the management of CIPN. Materials and Methods: The up-to-date guidelines of ESMO (European Society for Medical Oncology), ASCO (American Society of Clinical Oncology), ONS (Oncology Nursing Soci-ety), NCI (National Cancer Institute), and NCCN (National Comprehensive Cancer Network) were reviewed and included in the manuscript. Results: The use of tricyclic antidepressant (TCA), selective serotonin norepinephrine reuptake inhibitor (SSNRI), pregabalin, and gabapentin are recommended as first-line treatment. Other treatment options were offered as second and third lines of treatment (lidocaine patches, capsaicin high-concentration patches, tramadol, and strong opioids, respectively); however, lower significance was demonstrated. Inconclusive results were found in the use of cannabi-noids, drug combinations, antiepileptics, antidepressants, and topical drugs. Conclusion: TCA, other antidepressants, and opioids could be recommended as treatment. Yet, we could not recommend an ideal therapeutic agent for the prevention or treatment of CIPN. Therefore, CIPN continues to be a challenge to clinicians and our patients.
AB - Background: Chemotherapy-induced peripheral neuropathy (CIPN) is considered a severe side effect of therapeutic agents with limited treatment options. The incidence of CIPN in cancer patients is approximately 3–7% in cytostatic monotherapy and as high as 38% in cases of polychemotherapy. The prevalence of CIPN was found to be 68% within the first month of chemotherapy treatment. In some cases, CIPN can resolve, partially or completely, after completion of the treatment; in other cases, it can remain for a long time and affect the patient's quality of life. Objective: The aim of this study is to present up-to-date data regarding available treatment options for the management of CIPN. Materials and Methods: The up-to-date guidelines of ESMO (European Society for Medical Oncology), ASCO (American Society of Clinical Oncology), ONS (Oncology Nursing Soci-ety), NCI (National Cancer Institute), and NCCN (National Comprehensive Cancer Network) were reviewed and included in the manuscript. Results: The use of tricyclic antidepressant (TCA), selective serotonin norepinephrine reuptake inhibitor (SSNRI), pregabalin, and gabapentin are recommended as first-line treatment. Other treatment options were offered as second and third lines of treatment (lidocaine patches, capsaicin high-concentration patches, tramadol, and strong opioids, respectively); however, lower significance was demonstrated. Inconclusive results were found in the use of cannabi-noids, drug combinations, antiepileptics, antidepressants, and topical drugs. Conclusion: TCA, other antidepressants, and opioids could be recommended as treatment. Yet, we could not recommend an ideal therapeutic agent for the prevention or treatment of CIPN. Therefore, CIPN continues to be a challenge to clinicians and our patients.
KW - CIPN
KW - Cannabis
KW - Chemotherapy
KW - Neuropathy
KW - Opioid
KW - SSNR1
KW - TCA
UR - http://www.scopus.com/inward/record.url?scp=85066899600&partnerID=8YFLogxK
U2 - 10.2174/0929867326666190107163756
DO - 10.2174/0929867326666190107163756
M3 - Review article
C2 - 30621553
AN - SCOPUS:85066899600
SN - 0929-8673
VL - 26
SP - 4698
EP - 4708
JO - Current Medicinal Chemistry
JF - Current Medicinal Chemistry
IS - 25
ER -