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Effectiveness of fentanyl pectin nasal citrate in controlling episodes of breakthrough cancer pain triggered by routine radiotherapy procedures

Purpose The aim of the study was to evaluate the effectiveness of fentanyl pectin nasal spray (FPNS) in controlling procedural breakthrough cancer pain (BTCP) in advanced cancer patients undergoing radiotherapy. Materials and methods This study involved 62 advanced cancer patients, with well-control...

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Published in:Clinical & translational oncology 2019-11, Vol.21 (11), p.1568-1572
Main Authors: Pardo, J., Mena, A., Jiménez, E., Aymar, N., Ortiz, I., Roncero, R., Mestre, F., Vidal, M.
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cited_by cdi_FETCH-LOGICAL-c347t-e63c34804d77aff81eb09a24d3b61b095be3214613fa5a700b954a7a6a3b37be3
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container_end_page 1572
container_issue 11
container_start_page 1568
container_title Clinical & translational oncology
container_volume 21
creator Pardo, J.
Mena, A.
Jiménez, E.
Aymar, N.
Ortiz, I.
Roncero, R.
Mestre, F.
Vidal, M.
description Purpose The aim of the study was to evaluate the effectiveness of fentanyl pectin nasal spray (FPNS) in controlling procedural breakthrough cancer pain (BTCP) in advanced cancer patients undergoing radiotherapy. Materials and methods This study involved 62 advanced cancer patients, with well-controlled background pain, who presented BTCP associated to routine radiotherapy procedures, treated with FPNS according to our protocol of administration. The BPE intensity was measured using a visual analog scale (VAS). Results The BTCP was triggered during the computed tomography simulation (79.3%) or treatment delivery (20.7%). Patients indicated a mean VAS of 8.8 (range 7–10) when attempting the procedure. After 4.5 min (range 2–10) of the first FPNS dose, the majority of patients (85.5%) indicated a VAS of 4.3 (range 2–6). 15.5% of the patients did not respond after 15 min; requiring a second dose. All these patients responded, reporting a mean VAS of 4.2 (range 4–6) after 3.0 min (range 2–5) of the second dose. None of the patients required a third dose, nor reported an AE after the administration of FPNS. Conclusions In our knowledge, our study is the one of highest recruitment, and with the fastest response of BTCP treated with FPNS reported in advanced cancer patients undergoing radiotherapy. FPNS has proven to be highly effective in reducing the intensity of procedural BTCP in a very short period of time.
doi_str_mv 10.1007/s12094-019-02125-8
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Materials and methods This study involved 62 advanced cancer patients, with well-controlled background pain, who presented BTCP associated to routine radiotherapy procedures, treated with FPNS according to our protocol of administration. The BPE intensity was measured using a visual analog scale (VAS). Results The BTCP was triggered during the computed tomography simulation (79.3%) or treatment delivery (20.7%). Patients indicated a mean VAS of 8.8 (range 7–10) when attempting the procedure. After 4.5 min (range 2–10) of the first FPNS dose, the majority of patients (85.5%) indicated a VAS of 4.3 (range 2–6). 15.5% of the patients did not respond after 15 min; requiring a second dose. All these patients responded, reporting a mean VAS of 4.2 (range 4–6) after 3.0 min (range 2–5) of the second dose. None of the patients required a third dose, nor reported an AE after the administration of FPNS. Conclusions In our knowledge, our study is the one of highest recruitment, and with the fastest response of BTCP treated with FPNS reported in advanced cancer patients undergoing radiotherapy. FPNS has proven to be highly effective in reducing the intensity of procedural BTCP in a very short period of time.</description><identifier>ISSN: 1699-048X</identifier><identifier>EISSN: 1699-3055</identifier><identifier>DOI: 10.1007/s12094-019-02125-8</identifier><identifier>PMID: 31093890</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Analgesics, Opioid - administration &amp; dosage ; Breakthrough Pain - drug therapy ; Breakthrough Pain - etiology ; Cancer Pain - drug therapy ; Cancer Pain - etiology ; Female ; Fentanyl - administration &amp; dosage ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Nasal Sprays ; Neoplasms - radiotherapy ; Oncology ; Pain Measurement ; Pain, Procedural - complications ; Pain, Procedural - drug therapy ; Radiotherapy - adverse effects ; Research Article</subject><ispartof>Clinical &amp; translational oncology, 2019-11, Vol.21 (11), p.1568-1572</ispartof><rights>Federación de Sociedades Españolas de Oncología (FESEO) 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-e63c34804d77aff81eb09a24d3b61b095be3214613fa5a700b954a7a6a3b37be3</citedby><cites>FETCH-LOGICAL-c347t-e63c34804d77aff81eb09a24d3b61b095be3214613fa5a700b954a7a6a3b37be3</cites><orcidid>0000-0003-0921-0066</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31093890$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pardo, J.</creatorcontrib><creatorcontrib>Mena, A.</creatorcontrib><creatorcontrib>Jiménez, E.</creatorcontrib><creatorcontrib>Aymar, N.</creatorcontrib><creatorcontrib>Ortiz, I.</creatorcontrib><creatorcontrib>Roncero, R.</creatorcontrib><creatorcontrib>Mestre, F.</creatorcontrib><creatorcontrib>Vidal, M.</creatorcontrib><title>Effectiveness of fentanyl pectin nasal citrate in controlling episodes of breakthrough cancer pain triggered by routine radiotherapy procedures</title><title>Clinical &amp; translational oncology</title><addtitle>Clin Transl Oncol</addtitle><addtitle>Clin Transl Oncol</addtitle><description>Purpose The aim of the study was to evaluate the effectiveness of fentanyl pectin nasal spray (FPNS) in controlling procedural breakthrough cancer pain (BTCP) in advanced cancer patients undergoing radiotherapy. Materials and methods This study involved 62 advanced cancer patients, with well-controlled background pain, who presented BTCP associated to routine radiotherapy procedures, treated with FPNS according to our protocol of administration. The BPE intensity was measured using a visual analog scale (VAS). Results The BTCP was triggered during the computed tomography simulation (79.3%) or treatment delivery (20.7%). Patients indicated a mean VAS of 8.8 (range 7–10) when attempting the procedure. After 4.5 min (range 2–10) of the first FPNS dose, the majority of patients (85.5%) indicated a VAS of 4.3 (range 2–6). 15.5% of the patients did not respond after 15 min; requiring a second dose. All these patients responded, reporting a mean VAS of 4.2 (range 4–6) after 3.0 min (range 2–5) of the second dose. None of the patients required a third dose, nor reported an AE after the administration of FPNS. 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translational oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pardo, J.</au><au>Mena, A.</au><au>Jiménez, E.</au><au>Aymar, N.</au><au>Ortiz, I.</au><au>Roncero, R.</au><au>Mestre, F.</au><au>Vidal, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effectiveness of fentanyl pectin nasal citrate in controlling episodes of breakthrough cancer pain triggered by routine radiotherapy procedures</atitle><jtitle>Clinical &amp; translational oncology</jtitle><stitle>Clin Transl Oncol</stitle><addtitle>Clin Transl Oncol</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>21</volume><issue>11</issue><spage>1568</spage><epage>1572</epage><pages>1568-1572</pages><issn>1699-048X</issn><eissn>1699-3055</eissn><abstract>Purpose The aim of the study was to evaluate the effectiveness of fentanyl pectin nasal spray (FPNS) in controlling procedural breakthrough cancer pain (BTCP) in advanced cancer patients undergoing radiotherapy. 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subjects Adult
Aged
Aged, 80 and over
Analgesics, Opioid - administration & dosage
Breakthrough Pain - drug therapy
Breakthrough Pain - etiology
Cancer Pain - drug therapy
Cancer Pain - etiology
Female
Fentanyl - administration & dosage
Humans
Male
Medicine
Medicine & Public Health
Middle Aged
Nasal Sprays
Neoplasms - radiotherapy
Oncology
Pain Measurement
Pain, Procedural - complications
Pain, Procedural - drug therapy
Radiotherapy - adverse effects
Research Article
title Effectiveness of fentanyl pectin nasal citrate in controlling episodes of breakthrough cancer pain triggered by routine radiotherapy procedures
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