Real-world impact of granulocyte-colony stimulating factor on febrile neutropenia

被引:18
作者
Altwairgi, A. K. [1 ,2 ]
Hopman, W. M. [3 ,4 ]
Mates, M. [1 ]
机构
[1] Queens Univ, Canc Ctr Southeastern Ontario, Kingston, ON, Canada
[2] King Fahad Med City, Ctr Comprehens Canc, Riyadh 11525, Saudi Arabia
[3] Queens Univ, Kingston Gen Hosp, Clin Res Ctr, Kingston, ON, Canada
[4] Queens Univ, Dept Community Hlth & Epidemiol, Kingston, ON, Canada
关键词
Adjuvant chemotherapy; early-stage breast cancer; febrile neutropenia; filgrastim; pegfilgrastim; practice patterns; primary prophylaxis with granulocyte colony-stimulating factors; SINGLE-ADMINISTRATION PEGFILGRASTIM; CHEMOTHERAPY-INDUCED NEUTROPENIA; POSITIVE BREAST-CANCER; FEC-D CHEMOTHERAPY; EORTC GUIDELINES; DAILY FILGRASTIM; ADULT PATIENTS; GROWTH-FACTORS; DOUBLE-BLIND; HIGH-RISK;
D O I
10.3747/co.20.1306
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Primary prophylaxis with granulocyte colony-stimulating factors (PP-G-CSF) is recommended in patients undergoing chemotherapy carrying a febrile neutropenia (FN) risk of 20% or more. In the present study, we examined clinical practice patterns and the impact of PP-G-CSF on FN incidence in women with early-stage breast cancer (EBC) treated with modern adjuvant chemotherapy (ACT). Methods This single-centre retrospective cohort study of women with ebc, who were identified from the pharmacy database and who received at least 1 cycle of modern act from January 2009 to December 2011, was conducted at the Cancer Centre of Southeastern Ontario. Data on patient demographics, pathology, stage distribution, chemotherapy, PP-G-CSF use, dose reductions, chemotherapy delays, treatment discontinuation, relative dose intensity, and fn events were collected. Chi-square tests, t-tests, univariate and multivariate logistic regression analyses, and nonparametric Mann-Whitney U-tests were used for data analysis. Results Of the 239 women eligible for analysis, 145 (61%) received PP-G-CSF, and 50 (21%) developed at least 1 episode of FN. Use of PP-G-CSF was associated with a significantly lower rate of FN (14% vs. 31%, p = 0.002) and trends to fewer dose delays (17% vs. 27%, p = 0.060) and dose reductions (19% vs. 25%, p = 0.28). Among women receiving PP-G-CSF, higher FN rates were associated with an age of 65 years or older, taxane-based chemotherapy, and prophylaxis with filgrastim. Conclusions Clinical practice patterns at our institution showed that more than 50% of EBC patients treated with modern act received PP-G-CSF, which led to fewer FN episodes and increased delivery of planned act. The observed high FN risk despite PP-G-CSF was linked to older age, taxane-based chemotherapy, and filgrastim.
引用
收藏
页码:E171 / E179
页数:9
相关论文
共 41 条
[31]   2006 update of recommendations for the use of white blood cell growth factors: An evidence-based clinical practice guideline [J].
Smith, Thomas J. ;
Khatcheressian, James ;
Lyman, Gary H. ;
Ozer, Howard ;
Armitage, James O. ;
Balducci, Lodovico ;
Bennett, Charles L. ;
Cantor, Scott B. ;
Crawford, Jeffrey ;
Cross, Scott J. ;
Demetri, George ;
Desch, Christopher E. ;
Pizzo, Philip A. ;
Schiffer, Charles A. ;
Schwartzberg, Lee ;
Somerfield, Mark R. ;
Somlo, George ;
Wade, James C. ;
Wade, James L. ;
Winn, Rodger J. ;
Wozniak, Antoinette J. ;
Wolff, Antonio C. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (19) :3187-3205
[32]   High Rate of Febrile Neutropenia in Patients With Operable Breast Cancer Receiving Docetaxel and Cyclophosphamide [J].
Soong, Derrick ;
Haj, Reem ;
Leung, Mova G. ;
Myers, Robert ;
Higgins, Brian ;
Myers, Jeff ;
Rajagopal, Sudha .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (26) :E101-E102
[33]   Feasibility Study of Docetaxel with Cyclophosphamide as Adjuvant Chemotherapy for Japanese Breast Cancer Patients [J].
Takabatake, Daisuke ;
Taira, Naruto ;
Hara, Fumikata ;
Sien, Tadahiko ;
Kiyoto, Sachiko ;
Takashima, Seiki ;
Aogi, Kenjiro ;
Ohsumi, Shozo ;
Doihara, Hiroyoshi ;
Takashima, Shigemitu .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 39 (08) :478-483
[34]   Comparative effectiveness of colony-stimulating factors for febrile neutropenia: a retrospective study [J].
Tan, Hiangkiat ;
Tomic, Karen ;
Hurley, Dana ;
Daniel, Gregory ;
Barron, Rich ;
Malin, Jen .
CURRENT MEDICAL RESEARCH AND OPINION, 2011, 27 (01) :79-86
[35]   Prophylactic G-CSF and antibiotics enable a significant dose-escalation of triplet-chemotherapy in non-small cell lung cancer [J].
Timmer-Bonte, J. N. H. ;
Punta, C. J. A. ;
van der Heijden, H. F. M. ;
van Die, C. E. ;
Bussink, J. ;
Beijnen, J. H. ;
Huitema, A. D. R. ;
Tjan-Heijnen, V. C. G. .
LUNG CANCER, 2008, 60 (02) :222-230
[36]   RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR REDUCES THE INFECTIOUS COMPLICATIONS OF CYTOTOXIC CHEMOTHERAPY [J].
TRILLETLENOIR, V ;
GREEN, J ;
MANEGOLD, C ;
VONPAWEL, J ;
GATZEMEIER, U ;
LEBEAU, B ;
DEPIERRE, A ;
JOHNSON, P ;
DECOSTER, G ;
TOMITA, D ;
EWEN, C .
EUROPEAN JOURNAL OF CANCER, 1993, 29A (03) :319-324
[37]  
Vandenberg T, 2010, CURR ONCOL, V17, P56
[38]   First and subsequent cycle use of pegfilgrastim prevents febrile neutropenia in patients with breast cancer: A multicenter, double-blind, placebo-controlled phase III study [J].
Vogel, CL ;
Wojtukiewicz, MZ ;
Carroll, RR ;
Tjulandin, SA ;
Barajas-Figueroa, LJ ;
Wiens, BL ;
Neumann, TA ;
Schwartzberg, LS .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (06) :1178-1184
[39]   Filgrastim (r-metHuG-CSF): The first 10 years [J].
Welte, K ;
Gabrilove, J ;
Bronchud, MH ;
Platzer, E ;
Morstyn, G .
BLOOD, 1996, 88 (06) :1907-1929
[40]   Serum pegfilgrastim concentrations during recovery of absolute neutrophil count in patients with cancer receiving pegfilgrastim after chemotherapy [J].
Yang, Bing-Bing ;
Kido, Anna ;
Shibata, Atsuko .
PHARMACOTHERAPY, 2007, 27 (10) :1387-1393