Current developments in opioid therapy for management of cancer pain

被引:25
作者
de Leon-Casasola, Oscar A. [1 ,2 ]
机构
[1] SUNY Buffalo, Sch Med & Biomed Sci, Buffalo, NY 14260 USA
[2] Roswell Pk Canc Inst, Dept Anesthesiol & Pain Med, Buffalo, NY 14263 USA
关键词
D O I
10.1097/AJP.0b013e31816b589f
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Pain remains a highly prevalent problem for patients with cancer and typically falls into one of 3 types: visceral, somatic, and neuropathic. A mechanistic, pathophysiologic approach to pain management involves a good assessment of the type of pain, followed by tailoring of the treatment based on the diagnosis. This pain management strategy can provide rapid pain control with a lower incidence of complications and side effects than other methods. Furthermore, pharmacogenetics may play an important role in individualizing therapies in the future, but for now this type of data offers explanations for phenomena commonly observed in clinical practice, such as (1) differences in individual analgesic and side-effect responses to various opioid agents, (2) incomplete cross-tolerance seen when switching between p opioid analgesics, and (3) why opioid rotation can be beneficial for patients after an opioid therapy loses eificacy or becomes associated with intolerable side effects. Especially for difficult-to-manage pain patients, additions to the opioid analgesic armamentarium can potentially better individualize pain management, and provide another option to be used for, opioid rotation. Among the most recent Food and Drug Administration-approved opioid analgesics for acute pain and persistent pain are oral immediate-release and extended-release formulations of oxymorphone, whereas for breakthrough pain, the ultrarapid-acting opioid, fentanyl effervescent buccal tablets, has newly been developed and indicated within the United States.
引用
收藏
页码:S3 / S7
页数:5
相关论文
共 33 条
[1]   Oxymorphone extended release does not affect CYP2C9 or CYP3A4 metabolic pathways [J].
Adams, M ;
Pieniaszek, HJ ;
Gammaitoni, AR ;
Ahdieh, H .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (03) :337-345
[2]   Single- and multiple-dose pharmacokinetic and dose-proportionality study of oxymorphone immediate-release tablets [J].
Adams M.P. ;
Ahdieh H. .
Drugs in R & D, 2005, 6 (2) :91-99
[3]  
[Anonymous], 1990, WHO TECH REP SER, V804, P1
[4]  
Basbuam A.L., 2000, The perception of pain. Principles of Neural Science, P472
[5]  
Cadet P, 2004, MED SCI MONITOR, V10, pMS28
[6]   Relative bioavailability of the fentanyl effervescent buccal tablet (FEBT) 1080 μg versus oral transmucosal fentanyl citrate 1600 μg and dose proportionality of FEBT 270 to 1300 μg:: A single-dose, randomized, open-label, three-period study in healthy adult volunteers [J].
Darwish, M ;
Tempero, K ;
Kirby, M ;
Thompson, J .
CLINICAL THERAPEUTICS, 2006, 28 (05) :715-724
[7]   Pharmacokinetics and dose proportionality of fentanyl effervescent buccal tablets in healthy volunteers [J].
Darwish, M ;
Tempero, K ;
Kirby, M ;
Thompson, J .
CLINICAL PHARMACOKINETICS, 2005, 44 (12) :1279-1286
[8]   Multimodal approaches to the management of neuropathic pain: The role of topical analgesia [J].
de Leon-Casasola, Oscar A. .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2007, 33 (03) :356-364
[9]   Identification of five mouse μ-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon [J].
Doyle, Glenn A. ;
Sheng, X. Rebecca ;
Lin, Sharon S. J. ;
Press, Danielle M. ;
Grice, Dorothy E. ;
Buono, Russell J. ;
Ferraro, Thomas N. ;
Berrettini, Wade H. .
GENE, 2007, 395 (1-2) :98-107
[10]   Advances in neuropathic pain - Diagnosis, mechanisms, and treatment recommendations [J].
Dworkin, RH ;
Backonja, M ;
Rowbotham, MC ;
Allen, RR ;
Argoff, CR ;
Bennett, GJ ;
Bushnell, MC ;
Farrar, JT ;
Galer, BS ;
Haythornthwaite, JA ;
Hewitt, DJ ;
Loeser, JD ;
Max, MB ;
Saltarelli, M ;
Schmader, KE ;
Stein, C ;
Thompson, D ;
Turk, DC ;
Wallace, MS ;
Watkins, LR ;
Weinstein, SM .
ARCHIVES OF NEUROLOGY, 2003, 60 (11) :1524-1534