Time trends in utilization of G-CSF prophylaxis and risk of febrile neutropenia in a Medicare population receiving adjuvant chemotherapy for early-stage breast cancer

被引:11
作者
Goyal, Ravi K. [1 ]
Tzivelekis, Spiros [2 ]
Rothman, Kenneth J. [3 ]
Candrilli, Sean D. [1 ]
Kaye, James A. [3 ]
机构
[1] RTI Hlth Solut, 300 Pk Offices Dr, Res Triangle Pk, NC 27709 USA
[2] Amgen Inc, One Amgen Ctr Dr, Thousand Oaks, CA 91320 USA
[3] RTI Hlth Solut, 307 Waverley Oaks Rd,Suite 101, Waltham, MA 02452 USA
关键词
G-CSF; Febrile neutropenia; Prophylaxis; Breast cancer; Chemotherapy; Time trends; COLONY-STIMULATING FACTOR; HEALTH-CARE COSTS; CELL LUNG-CANCER; PHASE-III; IMPROVED OUTCOMES; RANDOMIZED-TRIAL; GUIDELINE; CYCLOPHOSPHAMIDE; HOSPITALIZATIONS; RECOMMENDATIONS;
D O I
10.1007/s00520-017-3863-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study is to assess temporal trends in the use of granulocyte colony-stimulating factor (G-CSF) prophylaxis and risk of febrile neutropenia (FN) among older women receiving adjuvant chemotherapy for early-stage breast cancer. Women aged ae<yen> 66 years with diagnosis of early-stage breast cancer who initiated selected adjuvant chemotherapy regimens were identified using the SEER-Medicare data from 2002 to 2012. Adjusted, calendar-year-specific proportions were estimated for use of G-CSF primary prophylaxis (PP) and secondary prophylaxis and FN risk in the first and the second/subsequent cycles during the first course of chemotherapy, using logistic regression models. calendar-year-specific mean probabilities were estimated with covariates set to modal values. Among 11,107 eligible patients (mean age 71.7 years), 74% received G-CSF in the first course of chemotherapy. Of all patients, 5819 (52%) received G-CSF PP, and among those not receiving G-CSF PP, only 5% received G-CSF secondary prophylaxis. The adjusted proportion using G-CSF PP increased from 6% in 2002 to 71% in 2012. During the same period, the adjusted risk of FN in the first cycle increased from 2% to 3%; the adjusted risk increased from 1.5% to 2.9% among those receiving G-CSF PP and from 2.3% to 3.5% among those not receiving G-CSF PP. The use of G-CSF PP increased substantially during the study period. Although channeling of higher-risk patients to treatment with G-CSF PP is expected, the adjusted risk of FN among patients treated with G-CSF PP tended to be lower than among those not receiving G-CSF PP.
引用
收藏
页码:539 / 548
页数:10
相关论文
共 35 条
[1]  
[Anonymous], 1994, J CLIN ONCOL, V12, P2471
[2]  
[Anonymous], SEER MED LINK DAT
[3]  
[Anonymous], 2016, Clinical Practice Guidelines in Oncology
[4]  
[Anonymous], 2016, CANC FACTS FIG 2015
[5]   The Charlson comorbidity index is adapted to predict costs of chronic disease in primary care patients [J].
Charlson, Mary E. ;
Charlson, Robert E. ;
Peterson, Janey C. ;
Marinopoulos, Spyridon S. ;
Briggs, William M. ;
Hollenberg, James P. .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2008, 61 (12) :1234-1240
[6]   Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741 [J].
Citron, ML ;
Berry, DA ;
Cirrincione, C ;
Hudis, C ;
Winer, EP ;
Gradishar, WJ ;
Davidson, NE ;
Martino, S ;
Livingston, R ;
Ingle, JN ;
Perez, EA ;
Carpenter, J ;
Hurd, D ;
Holland, JF ;
Smith, BL ;
Sartor, CI ;
Leung, EH ;
Abrams, J ;
Schilsky, RL ;
Muss, HB ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) :1431-1439
[7]   Impact of chemotherapy-induced neutropenia on quality of life: a prospective pilot investigation [J].
Fortner, BV ;
Schwartzberg, L ;
Tauer, K ;
Houts, AC ;
Hackett, J ;
Stolshek, BS .
SUPPORTIVE CARE IN CANCER, 2005, 13 (07) :522-528
[8]  
Goyal Ravi K, 2014, N C Med J, V75, P231
[9]  
Griffiths R. I., 2014, ISRN ONCOL, V2014, P607850, DOI [10.1155/2014/607850, DOI 10.1155/2014/607850]
[10]   Improved outcomes from adding sequential paclitaxel but not from escalating doxorubicin dose in an adjuvant chemotherapy regimen for patients with node-positive primary breast cancer [J].
Henderson, IC ;
Berry, DA ;
Demetri, GD ;
Cirrincione, CT ;
Goldstein, LJ ;
Martino, S ;
Ingle, JN ;
Cooper, MR ;
Hayes, DF ;
Tkaczuk, KH ;
Fleming, G ;
Holland, JF ;
Duggan, DB ;
Carpenter, JT ;
Frei, E ;
Schilsky, RL ;
Wood, WC ;
Muss, HB ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (06) :976-983