Cost benefit analysis of prophylactic granulocyte colony stimulating factor during CHOP antineoplastic therapy for non-Hodgkin's lymphoma

被引:13
作者
Dranitsaris, G
Altmayer, C
Quirt, I
机构
[1] Department of Pharmacy, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ont.
[2] Department of Medical Oncology, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ont.
[3] Dept. of Pharmaceutical Services, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ont. M5G 2M9
关键词
D O I
10.2165/00019053-199711060-00005
中图分类号
F [经济];
学科分类号
02 ;
摘要
Several randomised comparative trials have shown that granulocyte colony-stimulating factor (G-CSF) reduces the duration of neutropenia, hospitalisation and intravenous antibacterial use ill patients with cancer who are receiving high-dosage antineoplastic therapy. However, one area that has received less attention is the role of G-CSF in standard-dosage antineoplastic regimens. One such treatment that is considered to have a low potential fur inducing fever and neutropenia is the CHOP regimen (cyclophosphamide, doxorubicin, vincristine and prednisone) for non-Hodgkin's lymphoma. We conducted a cost-benefit analysis from a societal perspective in order to estimate the net cost or benefit of prophylactic G-CSF in this patient population. This included direct costs for hospitalisation with antibacterial support, as well as indirect societal costs, such as time off work and antineoplastic therapy delays secondary to neutropenia. The findings were then tested by a comprehensive sensitivity analysis. The administration of G-CSF at a dosage of 5 mu g/kg/day for 11 doses following CHOP resulted in an overall net cost of $Can1257. In the sensitivity analysis, lowering the G-CSF dosage to 2 mu g/kg/day generated a net benefit of $Can6564, indicating a situation that was cost saving to society, The results of the current study suggest that the use of G-CSF in patients receiving CHOP antineoplastic therapy produces a situation that is close to achieving cost neutrality. However, low-dosage (2 mu g/kg/day) G-CSF is an economically attractive treatment strategy because it may result in overall savings to society.
引用
收藏
页码:566 / 577
页数:12
相关论文
共 33 条
[1]  
*AM CANC SOC, 1995, CANC FACTS FIG, P14
[2]   CHEMOPROPHYLAXIS WITH ORAL CIPROFLOXACIN IN OVARIAN-CANCER PATIENTS RECEIVING TAXOL [J].
CARLSON, JW ;
FOWLER, JM ;
SALTZMAN, AK ;
CARTER, JR ;
CHEN, MD ;
MITCHELL, SK ;
DUNN, D ;
CARSON, LF ;
ADCOCK, LL ;
TWIGGS, LB .
GYNECOLOGIC ONCOLOGY, 1994, 55 (03) :415-420
[3]   REDUCTION BY GRANULOCYTE COLONY-STIMULATING FACTOR OF FEVER AND NEUTROPENIA INDUCED BY CHEMOTHERAPY IN PATIENTS WITH SMALL-CELL LUNG-CANCER [J].
CRAWFORD, J ;
OZER, H ;
STOLLER, R ;
JOHNSON, D ;
LYMAN, G ;
TABBARA, I ;
KRIS, M ;
GROUS, J ;
PICOZZI, V ;
RAUSCH, G ;
SMITH, R ;
GRADISHAR, W ;
YAHANDA, A ;
VINCENT, M ;
STEWART, M ;
GLASPY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (03) :164-170
[4]   COMPARISON OF CIPROFLOXACIN, OFLOXACIN AND PEFLOXACIN FOR THE PREVENTION OF THE BACTERIAL-INFECTION IN NEUTROPENIC PATIENTS WITH HEMATOLOGICAL MALIGNANCIES [J].
DANTONIO, D ;
PICCOLOMINI, R ;
IACONE, A ;
FIORITONI, G ;
PARRUTI, G ;
BETTI, S ;
QUAGLIETTA, AM ;
ACCORSI, P ;
DELLISOLA, M ;
FAVALLI, C .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (04) :837-844
[5]   CHEMOPROPHYLAXIS OF BACTERIAL-INFECTIONS IN GRANULOCYTOPENIC PATIENTS WITH CIPROFLOXACIN [J].
DENNIG, D ;
FULLE, HH ;
HELLRIEGEL, KP .
ONKOLOGIE, 1987, 10 (01) :57-58
[6]  
DEVITA VT, 1975, LANCET, V1, P248
[7]   ECONOMIC-ANALYSIS OF PROPHYLACTIC G-CSF AFTER MINI-BEAM SALVAGE CHEMOTHERAPY FOR HODGKINS AND NON-HODGKINS-LYMPHOMA [J].
DRANITSARIS, G ;
SUTCLIFFE, SB .
LEUKEMIA & LYMPHOMA, 1995, 17 (1-2) :139-145
[8]  
Fazio M T, 1991, Oncol Nurs Forum, V18, P1411
[9]   COMPARISON OF A STANDARD REGIMEN (CHOP) WITH 3 INTENSIVE CHEMOTHERAPY REGIMENS FOR ADVANCED NON-HODGKINS-LYMPHOMA [J].
FISHER, RI ;
GAYNOR, ER ;
DAHLBERG, S ;
OKEN, MM ;
GROGAN, TM ;
MIZE, EM ;
GLICK, JH ;
COLTMAN, CA ;
MILLER, TP .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (14) :1002-1006
[10]   EFFECT OF GRANULOCYTE COLONY-STIMULATING FACTOR ON NEUTROPENIA AND ASSOCIATED MORBIDITY DUE TO CHEMOTHERAPY FOR TRANSITIONAL-CELL CARCINOMA OF THE UROTHELIUM [J].
GABRILOVE, JL ;
JAKUBOWSKI, A ;
SCHER, H ;
STERNBERG, C ;
WONG, G ;
GROUS, J ;
YAGODA, A ;
FAIN, K ;
MOORE, MAS ;
CLARKSON, B ;
OETTGEN, HF ;
ALTON, K ;
WELTE, K ;
SOUZA, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (22) :1414-1422