Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline
To provide evidence-based guidance on the optimum prevention and treatment approaches in the management of chemotherapy-induced peripheral neuropathies (CIPN) in adult cancer survivors. A systematic literature search identified relevant, randomized controlled trials (RCTs) for the treatment of CIPN....
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Veröffentlicht in: | Journal of clinical oncology 2014-06, Vol.32 (18), p.1941-1967 |
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container_end_page | 1967 |
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container_issue | 18 |
container_start_page | 1941 |
container_title | Journal of clinical oncology |
container_volume | 32 |
creator | HERSHMAN, Dawn L LACCHETTI, Christina PAICE, Judith SCHNEIDER, Bryan SMITH, Mary Lou SMITH, Tom TERSTRIEP, Shelby WAGNER-JOHNSTON, Nina BAK, Kate LOPRINZI, Charles L DWORKIN, Robert H LAVOIE SMITH, Ellen M BLEEKER, Jonathan CAVALETTI, Guido CHAUHAN, Cynthia GAVIN, Patrick LAVINO, Antoinette LUSTBERG, Maryam B |
description | To provide evidence-based guidance on the optimum prevention and treatment approaches in the management of chemotherapy-induced peripheral neuropathies (CIPN) in adult cancer survivors.
A systematic literature search identified relevant, randomized controlled trials (RCTs) for the treatment of CIPN. Primary outcomes included incidence and severity of neuropathy as measured by neurophysiologic changes, patient-reported outcomes, and quality of life.
A total of 48 RCTs met eligibility criteria and comprise the evidentiary basis for the recommendations. Trials tended to be small and heterogeneous, many with insufficient sample sizes to detect clinically important differences in outcomes. Primary outcomes varied across the trials, and in most cases, studies were not directly comparable because of different outcomes, measurements, and instruments used at different time points. The strength of the recommendations is based on the quality, amount, and consistency of the evidence and the balance between benefits and harms.
On the basis of the paucity of high-quality, consistent evidence, there are no agents recommended for the prevention of CIPN. With regard to the treatment of existing CIPN, the best available data support a moderate recommendation for treatment with duloxetine. Although the CIPN trials are inconclusive regarding tricyclic antidepressants (such as nortriptyline), gabapentin, and a compounded topical gel containing baclofen, amitriptyline HCL, and ketamine, these agents may be offered on the basis of data supporting their utility in other neuropathic pain conditions given the limited other CIPN treatment options. Further research on these agents is warranted. |
doi_str_mv | 10.1200/jco.2013.54.0914 |
format | Article |
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A systematic literature search identified relevant, randomized controlled trials (RCTs) for the treatment of CIPN. Primary outcomes included incidence and severity of neuropathy as measured by neurophysiologic changes, patient-reported outcomes, and quality of life.
A total of 48 RCTs met eligibility criteria and comprise the evidentiary basis for the recommendations. Trials tended to be small and heterogeneous, many with insufficient sample sizes to detect clinically important differences in outcomes. Primary outcomes varied across the trials, and in most cases, studies were not directly comparable because of different outcomes, measurements, and instruments used at different time points. The strength of the recommendations is based on the quality, amount, and consistency of the evidence and the balance between benefits and harms.
On the basis of the paucity of high-quality, consistent evidence, there are no agents recommended for the prevention of CIPN. With regard to the treatment of existing CIPN, the best available data support a moderate recommendation for treatment with duloxetine. Although the CIPN trials are inconclusive regarding tricyclic antidepressants (such as nortriptyline), gabapentin, and a compounded topical gel containing baclofen, amitriptyline HCL, and ketamine, these agents may be offered on the basis of data supporting their utility in other neuropathic pain conditions given the limited other CIPN treatment options. Further research on these agents is warranted.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/jco.2013.54.0914</identifier><identifier>PMID: 24733808</identifier><language>eng</language><publisher>Alexandria, VA: American Society of Clinical Oncology</publisher><subject><![CDATA[Adult ; Amines - therapeutic use ; Amitriptyline - administration & dosage ; Analgesics - therapeutic use ; Anticonvulsants - therapeutic use ; Antidepressive Agents, Tricyclic - therapeutic use ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - adverse effects ; Baclofen - administration & dosage ; Biological and medical sciences ; Comorbidity ; Cyclohexanecarboxylic Acids - therapeutic use ; Drug Therapy, Combination ; Duloxetine Hydrochloride ; Evidence-Based Medicine ; gamma-Aminobutyric Acid - therapeutic use ; Gels ; Humans ; Incidence ; Ketamine - administration & dosage ; Medical sciences ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Neoplasms - drug therapy ; Neuralgia - drug therapy ; Neuralgia - etiology ; Neuralgia - prevention & control ; Peripheral Nervous System Diseases - chemically induced ; Peripheral Nervous System Diseases - complications ; Peripheral Nervous System Diseases - drug therapy ; Peripheral Nervous System Diseases - physiopathology ; Peripheral Nervous System Diseases - prevention & control ; Quality of Life ; Randomized Controlled Trials as Topic ; Severity of Illness Index ; Survivors ; Thiophenes - therapeutic use ; Treatment Outcome ; Tumors ; United States]]></subject><ispartof>Journal of clinical oncology, 2014-06, Vol.32 (18), p.1941-1967</ispartof><rights>2015 INIST-CNRS</rights><rights>2014 by American Society of Clinical Oncology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-85141798b2b83c1f766b4be8dd0eecebbaf011e68d130829eabfc9d8d1ebf26b3</citedby><cites>FETCH-LOGICAL-c509t-85141798b2b83c1f766b4be8dd0eecebbaf011e68d130829eabfc9d8d1ebf26b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28562251$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24733808$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HERSHMAN, Dawn L</creatorcontrib><creatorcontrib>LACCHETTI, Christina</creatorcontrib><creatorcontrib>PAICE, Judith</creatorcontrib><creatorcontrib>SCHNEIDER, Bryan</creatorcontrib><creatorcontrib>SMITH, Mary Lou</creatorcontrib><creatorcontrib>SMITH, Tom</creatorcontrib><creatorcontrib>TERSTRIEP, Shelby</creatorcontrib><creatorcontrib>WAGNER-JOHNSTON, Nina</creatorcontrib><creatorcontrib>BAK, Kate</creatorcontrib><creatorcontrib>LOPRINZI, Charles L</creatorcontrib><creatorcontrib>DWORKIN, Robert H</creatorcontrib><creatorcontrib>LAVOIE SMITH, Ellen M</creatorcontrib><creatorcontrib>BLEEKER, Jonathan</creatorcontrib><creatorcontrib>CAVALETTI, Guido</creatorcontrib><creatorcontrib>CHAUHAN, Cynthia</creatorcontrib><creatorcontrib>GAVIN, Patrick</creatorcontrib><creatorcontrib>LAVINO, Antoinette</creatorcontrib><creatorcontrib>LUSTBERG, Maryam B</creatorcontrib><creatorcontrib>American Society of Clinical Oncology</creatorcontrib><title>Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>To provide evidence-based guidance on the optimum prevention and treatment approaches in the management of chemotherapy-induced peripheral neuropathies (CIPN) in adult cancer survivors.
A systematic literature search identified relevant, randomized controlled trials (RCTs) for the treatment of CIPN. Primary outcomes included incidence and severity of neuropathy as measured by neurophysiologic changes, patient-reported outcomes, and quality of life.
A total of 48 RCTs met eligibility criteria and comprise the evidentiary basis for the recommendations. Trials tended to be small and heterogeneous, many with insufficient sample sizes to detect clinically important differences in outcomes. Primary outcomes varied across the trials, and in most cases, studies were not directly comparable because of different outcomes, measurements, and instruments used at different time points. The strength of the recommendations is based on the quality, amount, and consistency of the evidence and the balance between benefits and harms.
On the basis of the paucity of high-quality, consistent evidence, there are no agents recommended for the prevention of CIPN. With regard to the treatment of existing CIPN, the best available data support a moderate recommendation for treatment with duloxetine. Although the CIPN trials are inconclusive regarding tricyclic antidepressants (such as nortriptyline), gabapentin, and a compounded topical gel containing baclofen, amitriptyline HCL, and ketamine, these agents may be offered on the basis of data supporting their utility in other neuropathic pain conditions given the limited other CIPN treatment options. Further research on these agents is warranted.</description><subject>Adult</subject><subject>Amines - therapeutic use</subject><subject>Amitriptyline - administration & dosage</subject><subject>Analgesics - therapeutic use</subject><subject>Anticonvulsants - therapeutic use</subject><subject>Antidepressive Agents, Tricyclic - therapeutic use</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Baclofen - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Comorbidity</subject><subject>Cyclohexanecarboxylic Acids - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Duloxetine Hydrochloride</subject><subject>Evidence-Based Medicine</subject><subject>gamma-Aminobutyric Acid - therapeutic use</subject><subject>Gels</subject><subject>Humans</subject><subject>Incidence</subject><subject>Ketamine - administration & dosage</subject><subject>Medical sciences</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Neoplasms - drug therapy</subject><subject>Neuralgia - drug therapy</subject><subject>Neuralgia - etiology</subject><subject>Neuralgia - prevention & control</subject><subject>Peripheral Nervous System Diseases - chemically induced</subject><subject>Peripheral Nervous System Diseases - complications</subject><subject>Peripheral Nervous System Diseases - drug therapy</subject><subject>Peripheral Nervous System Diseases - physiopathology</subject><subject>Peripheral Nervous System Diseases - prevention & control</subject><subject>Quality of Life</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Severity of Illness Index</subject><subject>Survivors</subject><subject>Thiophenes - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>United States</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUtv1DAUhS0EokNhzwp5g8Qmgx9x4rAbRVCKCjMSILGL_LjpuEri1E5Gyj_iZ-LQga6u7tF3zpXuQeg1JVvKCHl_Z_yWEcq3It-SiuZP0IYKVmZlKcRTtCElZxmV_NcFehHjHSE0l1w8RxcsLzmXRG7Q70OAEwyT8wNWg8Vf1aBuoU8K9i2uj9D76QhBjUt2PdjZgMUHCG5ctQ5_gzn4UU3HBbsBf5_DyZ18iKt1Z-duwrUaDIT4Ae_65DIqQd44mJa_6Z0bktbh_WB852-XR-UQlJmcAXw1OwtJhZfoWau6CK_O8xL9_PTxR_05u9lfXde7m8wIUk2ZFDSnZSU105Ib2pZFoXMN0loCYEBr1RJKoZCWciJZBUq3prJpBd2yQvNL9O4hdwz-foY4Nb2LBrpODeDn2FDBRcEYpVVCyQNqgo8xQNuMwfUqLA0lzdpP86XeN2s_jcibtZ9keXNOn3UP9r_hXyEJeHsGVEyPaEN6oIuPnFyPC8r_ALcdnLM</recordid><startdate>20140620</startdate><enddate>20140620</enddate><creator>HERSHMAN, Dawn L</creator><creator>LACCHETTI, Christina</creator><creator>PAICE, Judith</creator><creator>SCHNEIDER, Bryan</creator><creator>SMITH, Mary Lou</creator><creator>SMITH, Tom</creator><creator>TERSTRIEP, Shelby</creator><creator>WAGNER-JOHNSTON, Nina</creator><creator>BAK, Kate</creator><creator>LOPRINZI, Charles L</creator><creator>DWORKIN, Robert H</creator><creator>LAVOIE SMITH, Ellen M</creator><creator>BLEEKER, Jonathan</creator><creator>CAVALETTI, Guido</creator><creator>CHAUHAN, Cynthia</creator><creator>GAVIN, Patrick</creator><creator>LAVINO, Antoinette</creator><creator>LUSTBERG, Maryam B</creator><general>American Society of Clinical Oncology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140620</creationdate><title>Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline</title><author>HERSHMAN, Dawn L ; LACCHETTI, Christina ; PAICE, Judith ; SCHNEIDER, Bryan ; SMITH, Mary Lou ; SMITH, Tom ; TERSTRIEP, Shelby ; WAGNER-JOHNSTON, Nina ; BAK, Kate ; LOPRINZI, Charles L ; DWORKIN, Robert H ; LAVOIE SMITH, Ellen M ; BLEEKER, Jonathan ; CAVALETTI, Guido ; CHAUHAN, Cynthia ; GAVIN, Patrick ; LAVINO, Antoinette ; LUSTBERG, Maryam B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-85141798b2b83c1f766b4be8dd0eecebbaf011e68d130829eabfc9d8d1ebf26b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Amines - therapeutic use</topic><topic>Amitriptyline - administration & dosage</topic><topic>Analgesics - therapeutic use</topic><topic>Anticonvulsants - therapeutic use</topic><topic>Antidepressive Agents, Tricyclic - therapeutic use</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Baclofen - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Comorbidity</topic><topic>Cyclohexanecarboxylic Acids - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Duloxetine Hydrochloride</topic><topic>Evidence-Based Medicine</topic><topic>gamma-Aminobutyric Acid - therapeutic use</topic><topic>Gels</topic><topic>Humans</topic><topic>Incidence</topic><topic>Ketamine - administration & dosage</topic><topic>Medical sciences</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Neoplasms - drug therapy</topic><topic>Neuralgia - drug therapy</topic><topic>Neuralgia - etiology</topic><topic>Neuralgia - prevention & control</topic><topic>Peripheral Nervous System Diseases - chemically induced</topic><topic>Peripheral Nervous System Diseases - complications</topic><topic>Peripheral Nervous System Diseases - drug therapy</topic><topic>Peripheral Nervous System Diseases - physiopathology</topic><topic>Peripheral Nervous System Diseases - prevention & control</topic><topic>Quality of Life</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Severity of Illness Index</topic><topic>Survivors</topic><topic>Thiophenes - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HERSHMAN, Dawn L</creatorcontrib><creatorcontrib>LACCHETTI, Christina</creatorcontrib><creatorcontrib>PAICE, Judith</creatorcontrib><creatorcontrib>SCHNEIDER, Bryan</creatorcontrib><creatorcontrib>SMITH, Mary Lou</creatorcontrib><creatorcontrib>SMITH, Tom</creatorcontrib><creatorcontrib>TERSTRIEP, Shelby</creatorcontrib><creatorcontrib>WAGNER-JOHNSTON, Nina</creatorcontrib><creatorcontrib>BAK, Kate</creatorcontrib><creatorcontrib>LOPRINZI, Charles L</creatorcontrib><creatorcontrib>DWORKIN, Robert H</creatorcontrib><creatorcontrib>LAVOIE SMITH, Ellen M</creatorcontrib><creatorcontrib>BLEEKER, Jonathan</creatorcontrib><creatorcontrib>CAVALETTI, Guido</creatorcontrib><creatorcontrib>CHAUHAN, Cynthia</creatorcontrib><creatorcontrib>GAVIN, Patrick</creatorcontrib><creatorcontrib>LAVINO, Antoinette</creatorcontrib><creatorcontrib>LUSTBERG, Maryam B</creatorcontrib><creatorcontrib>American Society of Clinical Oncology</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HERSHMAN, Dawn L</au><au>LACCHETTI, Christina</au><au>PAICE, Judith</au><au>SCHNEIDER, Bryan</au><au>SMITH, Mary Lou</au><au>SMITH, Tom</au><au>TERSTRIEP, Shelby</au><au>WAGNER-JOHNSTON, Nina</au><au>BAK, Kate</au><au>LOPRINZI, Charles L</au><au>DWORKIN, Robert H</au><au>LAVOIE SMITH, Ellen M</au><au>BLEEKER, Jonathan</au><au>CAVALETTI, Guido</au><au>CHAUHAN, Cynthia</au><au>GAVIN, Patrick</au><au>LAVINO, Antoinette</au><au>LUSTBERG, Maryam B</au><aucorp>American Society of Clinical Oncology</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2014-06-20</date><risdate>2014</risdate><volume>32</volume><issue>18</issue><spage>1941</spage><epage>1967</epage><pages>1941-1967</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>To provide evidence-based guidance on the optimum prevention and treatment approaches in the management of chemotherapy-induced peripheral neuropathies (CIPN) in adult cancer survivors.
A systematic literature search identified relevant, randomized controlled trials (RCTs) for the treatment of CIPN. Primary outcomes included incidence and severity of neuropathy as measured by neurophysiologic changes, patient-reported outcomes, and quality of life.
A total of 48 RCTs met eligibility criteria and comprise the evidentiary basis for the recommendations. Trials tended to be small and heterogeneous, many with insufficient sample sizes to detect clinically important differences in outcomes. Primary outcomes varied across the trials, and in most cases, studies were not directly comparable because of different outcomes, measurements, and instruments used at different time points. The strength of the recommendations is based on the quality, amount, and consistency of the evidence and the balance between benefits and harms.
On the basis of the paucity of high-quality, consistent evidence, there are no agents recommended for the prevention of CIPN. With regard to the treatment of existing CIPN, the best available data support a moderate recommendation for treatment with duloxetine. Although the CIPN trials are inconclusive regarding tricyclic antidepressants (such as nortriptyline), gabapentin, and a compounded topical gel containing baclofen, amitriptyline HCL, and ketamine, these agents may be offered on the basis of data supporting their utility in other neuropathic pain conditions given the limited other CIPN treatment options. Further research on these agents is warranted.</abstract><cop>Alexandria, VA</cop><pub>American Society of Clinical Oncology</pub><pmid>24733808</pmid><doi>10.1200/jco.2013.54.0914</doi><tpages>27</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Amines - therapeutic use Amitriptyline - administration & dosage Analgesics - therapeutic use Anticonvulsants - therapeutic use Antidepressive Agents, Tricyclic - therapeutic use Antineoplastic Agents - administration & dosage Antineoplastic Agents - adverse effects Baclofen - administration & dosage Biological and medical sciences Comorbidity Cyclohexanecarboxylic Acids - therapeutic use Drug Therapy, Combination Duloxetine Hydrochloride Evidence-Based Medicine gamma-Aminobutyric Acid - therapeutic use Gels Humans Incidence Ketamine - administration & dosage Medical sciences Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Neoplasms - drug therapy Neuralgia - drug therapy Neuralgia - etiology Neuralgia - prevention & control Peripheral Nervous System Diseases - chemically induced Peripheral Nervous System Diseases - complications Peripheral Nervous System Diseases - drug therapy Peripheral Nervous System Diseases - physiopathology Peripheral Nervous System Diseases - prevention & control Quality of Life Randomized Controlled Trials as Topic Severity of Illness Index Survivors Thiophenes - therapeutic use Treatment Outcome Tumors United States |
title | Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline |
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