Tapentadol in the management of cancer pain: current evidence and future perspectives.

cancer pain neuropathic pain tapentadol

Journal

Journal of pain research
ISSN: 1178-7090
Titre abrégé: J Pain Res
Pays: New Zealand
ID NLM: 101540514

Informations de publication

Date de publication:
2019
Historique:
entrez: 14 6 2019
pubmed: 14 6 2019
medline: 14 6 2019
Statut: epublish

Résumé

Thanks to the progress in early diagnosis and treatment of cancer, the life expectancy of cancer patients has now increased. Patients are, therefore, more likely to experience their individual cancer pain as a chronic pain. As a consequence, long-term treatment of cancer-related pain and oncological therapy-related pain are a major need for all patients and a challenge to all healthcare professionals. Tapentadol is a centrally acting analgesic drug characterized by two synergistic mechanisms of action, since it acts at the µ-opioid receptor (MOR) and inhibits noradrenalin re-uptake (NRI). Therefore, tapentadol has been considered the first of a new class of drugs, MOR-NRI. Tapentadol has been tested in different populations of cancer patients (opioid-naive and -pretreated), such as those with pain of mixed etiology, patients with pain from hematological malignancies and patients experiencing pain conditions due to anticancer treatment. According to available evidence, tapentadol prolonged release was well tolerated and effective in cancer pain patients. In randomized, double-blind and active-controlled trials it proved non-inferior to standard opioids like morphine or oxycodone in the management of moderate-to-severe cancer pain, both in opioid-naive and in opioid-pretreated patients. The good analgesic efficacy may be partly due to the action of tapentadol on neuropathic pain components. Together with the low rate of gastrointestinal adverse effects and the overall favorable safety profile, tapentadol can be considered a good option in cancer pain patients, who can suffer frequently from nausea, vomiting, constipation or other events that further reduce their quality of life.

Identifiants

pubmed: 31190966
doi: 10.2147/JPR.S191543
pii: jpr-12-1553
pmc: PMC6526916
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1553-1560

Déclaration de conflit d'intérêts

Disclosure HGK has received speaker’s and/or consultancy fees from Bionorica SE, Grunenthal GmbH, Mundipharma Int., TEVA Ratiopharm, Mylan, and Pfizer outside the submit ted work. The authors report no other conflicts of interest in this work.

Références

Pain. 2005 Mar;114(1-2):29-36
pubmed: 15733628
Ann Oncol. 2009 Aug;20(8):1420-33
pubmed: 19244085
Eur J Pain. 2010 Sep;14(8):781-3
pubmed: 20659810
Pain. 2012 Feb;153(2):359-65
pubmed: 22115921
Lancet Oncol. 2012 Feb;13(2):e58-68
pubmed: 22300860
Drugs. 2012 Aug 20;72(12):1645-69
pubmed: 22867045
Ann Oncol. 2012 Oct;23 Suppl 7:vii139-54
pubmed: 22997447
Curr Med Res Opin. 2012 Nov;28(11):1775-9
pubmed: 23057488
Curr Med Res Opin. 2013 Jun;29(6):661-6
pubmed: 23540512
Pain. 2013 Jun;154(6):917-26
pubmed: 23582155
Br J Anaesth. 2013 Jul;111(1):105-11
pubmed: 23794652
Curr Med Res Opin. 2013 Oct;29(10):1399-409
pubmed: 23937387
Curr Opin Support Palliat Care. 2014 Jun;8(2):83-90
pubmed: 24792411
J Clin Oncol. 2014 Jun 1;32(16):1662-70
pubmed: 24799466
Clin Drug Investig. 2014 Jul;34(7):501-11
pubmed: 24906437
Curr Med Res Opin. 2014 Oct;30(10):2063-8
pubmed: 24926734
Pain Physician. 2014 Jul-Aug;17(4):329-43
pubmed: 25054392
J Pain Res. 2014 Dec 22;8:1-8
pubmed: 25565884
J Pain Res. 2015 May 08;8:229-38
pubmed: 26064064
Cochrane Database Syst Rev. 2015 Sep 25;(9):CD011460
pubmed: 26403220
Crit Rev Oncol Hematol. 2016 Mar;99:100-6
pubmed: 26712589
Cardiovasc Hematol Agents Med Chem. 2016;14(1):68-74
pubmed: 27048320
Eur J Pain. 2016 Oct;20(9):1513-8
pubmed: 27062079
J Pain Symptom Manage. 2016 Jun;51(6):1070-1090.e9
pubmed: 27112310
Support Care Cancer. 2016 Oct;24(10):4457
pubmed: 27480181
Br J Pain. 2016 Nov;10(4):217-221
pubmed: 27867511
Eur J Cancer. 2017 Jan;71:80-94
pubmed: 27984770
Eur J Pain. 2017 Jan;21(1):3-19
pubmed: 27991730
Neurol Sci. 2017 Oct;38(10):1747-1752
pubmed: 28699105
J Pain Res. 2017 Aug 31;10:2097-2107
pubmed: 28919809
J Pain Res. 2017 Sep 12;10:2147-2155
pubmed: 29066928
Clin Transl Oncol. 2018 Jan;20(1):97-107
pubmed: 29127593
Cancer Treat Rev. 2018 Feb;63:96-103
pubmed: 29272781
Expert Opin Drug Discov. 2018 Oct;13(10):965-972
pubmed: 30175624
Adv Ther. 2018 Oct;35(10):1471-1484
pubmed: 30206823
J Pain Res. 2018 Oct 29;11:2587-2601
pubmed: 30464578
J Pain Res. 2018 Dec 24;12:117-125
pubmed: 30613160

Auteurs

Hans G Kress (HG)

Department of Special Anesthesia and Pain Medicine, Medical University, Vienna General Hospital, Vienna, Austria, hans-georg.kress@meduniwien.ac.at.

Flaminia Coluzzi (F)

Department of Medical and Surgical Sciences and Biotechnologies, Unit of Anesthesia, Intensive Care and Pain Medicine, Sapienza University of Rome, Polo Pontino, Latina, Italy.

Classifications MeSH