Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain

被引:12
作者
Ueberall, Michael A. [1 ]
Lorenzl, Stefan [2 ]
Lux, Eberhard A. [3 ,4 ]
Voltz, Raymond [5 ]
Perelman, Michael [6 ]
机构
[1] Inst Neurol Sci, Nordostpk 51, D-90411 Nurnberg, Germany
[2] Paracelsus Private Med Univ Salzburg, Inst Nursing Sci & Practice, Salzburg, Austria
[3] Univ Witten Herdecke, Fac Med, Witten, Germany
[4] St Marien Hosp, Clin Pain & Palliat Care Med, Luenen, Germany
[5] Univ Hosp Cologne, Dept Palliat Med, Cologne, Germany
[6] Archimedes Dev Ltd, Nottingham, England
来源
JOURNAL OF PAIN RESEARCH | 2016年 / 9卷
关键词
breakthrough pain; cancer; fentanyl pectin nasal spray; intranasal administration; efficacy; safety; quality of life; OUTCOME MEASURES; VALIDATION; RECOMMENDATIONS; ACCEPTABILITY; MANAGEMENT; INTENSITY; CROSSOVER; MORPHINE; OPIOIDS;
D O I
10.2147/JPR.S106177
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Assessment of analgesic effectiveness, safety, and tolerability of fentanyl pectin nasal spray (FPNS) in the treatment of breakthrough cancer pain (BTcP) in routine clinical practice. Methods: A prospective, open-label, noninterventional study (4-week observation period, 3 month follow-up) of opioid-tolerant adults with BTcP in 41 pain and palliative care centers in Germany. Standardized BTcP questionnaires and patient diaries were used. Evaluation was made of patient-reported outcomes with respect to "time to first effect", "time to maximum effect", BTcP relief, as well as changes in BTcP-related impairment of daily life activities, quality-of-life restrictions, and health care resource utilization. Results: A total of 235 patients were recruited of whom 220 completed all questionnaires and reported on 1,569 BTcP episodes. Patients reported a significant reduction of maximum BTcP intensity (11-stage numerical rating scale [0= no pain, 10= worst pain conceivable]) with FPNS (mean +/- standard deviation = 2.8 +/- 2.3) compared with either that reported at baseline (8.5 +/- 1.5), experienced immediately before FPNS application (7.4 +/- 1.7), or that achieved with previous BTcP medication (6.0 +/- 2.0; P<0.001 for each comparison). In 12.3% of BTcP episodes, onset of pain relief occurred = 2 minutes and in 48.4% <= 5 minutes; maximum effects were reported within 10 minutes for 37.9% and within 15 minutes for 79.4%. By the end of the study, there had been significant improvements versus baseline in BTcP-related daily life activities (28.3 +/- 16.9 vs 53.1 +/- 11.9), physical (35.9 +/- 8.4 vs 26.8 +/- 6.5), and mental quality of life (38.7 +/- 8.5 vs 29.9 +/- 7.9) (P<0.001 for each comparison vs baseline); in addition, health care resource utilization requirements directly related to BTcP were reduced by 67.5%. FPNS was well tolerated; seven patients (3.2%) experienced eight treatment-emergent adverse events of which none was serious. There were no indicators of misuse or abuse. Conclusion: FPNS provided rapid and highly effective BTcP relief in opioid-tolerant cancer patients with substantial improvements in daily functioning and quality of life. FPNS was well tolerated and associated with significant reductions in health care resource utilization and nursing assistance.
引用
收藏
页码:571 / 585
页数:15
相关论文
共 36 条
[1]  
Abernethy Amy P, 2008, Am J Manag Care, V14, pS129
[2]  
[Anonymous], MED DICT REG ACT VER
[3]  
[Anonymous], 2006, CANC RELATED BREAKTH
[4]  
[Anonymous], WHOS PAIN LADD AD
[5]  
[Anonymous], PECFENT PECT FENT NA
[6]  
[Anonymous], 1996, CANC PAIN REL GUID O
[7]  
Bullinger M., 1998, SF-36 Fragebogen zum Gesundheitszustand - HandanweisungAufl
[8]   Breakthrough pain characteristics and syndromes in patients with cancer pain. An international survey [J].
Caraceni, A ;
Martini, C ;
Zecca, E ;
Portenoy, RK .
PALLIATIVE MEDICINE, 2004, 18 (03) :177-183
[9]   Use of opioid analgesics in the treatment of cancer pain: evidence-based recommendations from the EAPC [J].
Caraceni, Augusto ;
Hanks, Geoff Rey ;
Kaasa, Stein ;
Bennett, Michael I. ;
Brunelli, Cinzia ;
Cherny, Nathan ;
Dale, Ola ;
De Conno, Franco ;
Fallon, Marie ;
Hanna, Magdi ;
Haugen, Dagny Faksvag ;
Juhl, Gitte ;
King, Samuel ;
Klepstad, Pal ;
Laugsand, Eivor A. ;
Maltoni, Marco ;
Mercadante, Sebastiano ;
Nabal, Maria ;
Pigni, Alessandra ;
Radbruch, Lukas ;
Reid, Colette ;
Sjogren, Per ;
Stone, Patrick C. ;
Tassinari, Davide ;
Zeppetella, Giovambattista .
LANCET ONCOLOGY, 2012, 13 (02) :E58-E68
[10]   Development of in vitro models to demonstrate the ability of PecSys®, an in situ nasal gelling technology, to reduce nasal run-off and drip [J].
Castile, Jonathan ;
Cheng, Yu-Hui ;
Simmons, Ben ;
Perelman, Michael ;
Smith, Alan ;
Watts, Peter .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (05) :816-824