Cost analysis of using Magee scores as a surrogate of Oncotype DX for adjuvant treatment decisions in women with early breast cancer

被引:8
作者
de Lima, Mariana A. G. [1 ]
Clemons, Mark [2 ,3 ,4 ,5 ]
Van Katwyk, Sasha [2 ,5 ]
Stober, Carol [2 ]
Robertson, Susan J. [6 ]
Vandermeer, Lisa [2 ]
Fergusson, Dean [2 ,5 ]
Thavorn, Kednapa [2 ,5 ,7 ]
机构
[1] Univ Sao Paulo, Fac Med, Inst Canc State Sao Paulo, Sao Paulo, Brazil
[2] Ottawa Hosp Res Inst, Canc Res Program, Ottawa, ON, Canada
[3] Dept Med, Div Med Oncol, Ottawa, ON, Canada
[4] Univ Ottawa, Ottawa, ON, Canada
[5] Univ Ottawa, Sch Epidemiol & Publ Hlth, Ottawa, ON, Canada
[6] Univ Ottawa, Dept Pathol & Lab Med, Eastern Ontario Reg Lab Assoc, Ottawa, ON, Canada
[7] Univ Ottawa, Inst Clin & Evaluat Sci ICES uOttawa, Ottawa, ON, Canada
关键词
breast cancer; cost analysis; Magee equations; Oncotype DX; recurrence score; GENE-EXPRESSION; RECURRENCE; ASSAY; EQUATIONS; PREDICT; BENEFIT;
D O I
10.1111/jep.13223
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Breast cancer is the most common cancer in women worldwide. Most current guidelines recommend using multigene profiling assays to aid the decision on the addition of chemotherapy to adjuvant hormone therapy for women who present with early-stage, hormone receptor-positive, HER2-negative disease. One of these assays is the Oncotype DX, which predicts the disease recurrence risk and adjuvant chemotherapy benefits. Given its high cost, there is an economic incentive to evaluate its surrogates, such as the Magee equations. We assessed health system costs associated with the use of the Magee scores. A probabilistic decision tree was used to calculate the difference in mean health system costs based on data obtained from a randomized trial and the published literature. Costs were calculated from a perspective of Canada's publicly funded health care system. A series of sensitivity analysis was conducted to assess the robustness of the study findings. The Magee equations were associated with a total cost savings of C$100 per patient (95% CI, -C$3068 to C$5022) compared with standard of care. The difference in costs was highly sensitive to the extent that the Magee scores could reduce the frequency of adjuvant chemotherapy and Oncotype DX requests.
引用
收藏
页码:889 / 892
页数:4
相关论文
共 12 条
[1]   Histopathologic variables predict Oncotype DX™ Recurrence Score [J].
Flanagan, Melina B. ;
Dabbs, David J. ;
Brufsky, Adam M. ;
Beriwal, Sushil ;
Bhargava, Rohit .
MODERN PATHOLOGY, 2008, 21 (10) :1255-1261
[2]  
Hou YJ, 2017, AM J CLIN PATHOL, V147, P541, DOI [10.1093/AJCP/AQX008, 10.1093/ajcp/aqx008]
[3]   Agreement in Risk Prediction Between the 21-Gene Recurrence Score Assay (Oncotype DX®) and the PAM50 Breast Cancer Intrinsic Classifier™ in Early-Stage Estrogen Receptor-Positive Breast Cancer [J].
Kelly, Catherine M. ;
Bernard, Philip S. ;
Krishnamurthy, Savitri ;
Wang, Bailiang ;
Ebbert, Mark T. W. ;
Bastien, Roy R. L. ;
Boucher, Kenneth M. ;
Young, Elliana ;
Iwamoto, Takayuki ;
Pusztai, Lajos .
ONCOLOGIST, 2012, 17 (04) :492-498
[4]   Prediction of the Oncotype DX recurrence score: use of pathology-generated equations derived by linear regression analysis [J].
Klein, Molly E. ;
Dabbs, David J. ;
Shuai, Yongli ;
Brufsky, Adam M. ;
Jankowitz, Rachel ;
Puhalla, Shannon L. ;
Bhargava, Rohit .
MODERN PATHOLOGY, 2013, 26 (05) :658-664
[5]   Population-Based Study to Determine the Health System Costs of Using the 21-Gene Assay [J].
Mittmann, Nicole ;
Earle, Craig C. ;
Cheng, Stephanie Y. ;
Julian, Jim A. ;
Rahman, Farah ;
Seung, Soo Jin ;
Levine, Mark N. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (03) :238-+
[6]   A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer [J].
Paik, S ;
Shak, S ;
Tang, G ;
Kim, C ;
Baker, J ;
Cronin, M ;
Baehner, FL ;
Walker, MG ;
Watson, D ;
Park, T ;
Hiller, W ;
Fisher, ER ;
Wickerham, DL ;
Bryant, J ;
Wolmark, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (27) :2817-2826
[7]   Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer [J].
Paik, Soonmyung ;
Tang, Gong ;
Shak, Steven ;
Kim, Chungyeul ;
Baker, Joffre ;
Kim, Wanseop ;
Cronin, Maureen ;
Baehner, Frederick L. ;
Watson, Drew ;
Bryant, John ;
Costantino, Joseph P. ;
Geyer, Charles E., Jr. ;
Wickerham, D. Lawrence ;
Wolmark, Norman .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (23) :3726-3734
[8]   Does integration of Magee equations into routine clinical practice affect whether oncologists order the Oncotype DX test? A prospective randomized trial [J].
Robertson, Susan J. ;
Ibrahim, Mohammed F. K. ;
Stober, Carol ;
Hilton, John ;
Kos, Zuzana ;
Mazzarello, Sasha ;
Ramsay, Tim ;
Fergusson, Dean ;
Vandermeer, Lisa ;
Mallick, Ranjeeta ;
Arnaout, Angel ;
Dent, Susan F. ;
Segal, Roanne ;
Sehdev, Sandeep ;
Gertler, Stan ;
Hutton, Brian ;
Clemons, Mark .
JOURNAL OF EVALUATION IN CLINICAL PRACTICE, 2019, 25 (02) :196-204
[9]   MOLECULAR ORIGINS OF CANCER Gene-Expression Signatures in Breast Cancer [J].
Sotiriou, Christos ;
Pusztai, Lajos .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (08) :790-800
[10]   Adjuvant Chemotherapy Guided by a 21-Gene Expression Assay in Breast Cancer [J].
Sparano, J. A. ;
Gray, R. J. ;
Makower, D. F. ;
Pritchard, K. I. ;
Albain, K. S. ;
Hayes, D. F. ;
Geyer, C. E., Jr. ;
Dees, E. C. ;
Goetz, M. P. ;
Olson, J. A., Jr. ;
Lively, T. ;
Badve, S. S. ;
Saphner, T. J. ;
Wagner, L. I. ;
Whelan, T. J. ;
Ellis, M. J. ;
Paik, S. ;
Wood, W. C. ;
Ravdin, P. M. ;
Keane, M. M. ;
Moreno, H. L. Gomez ;
Reddy, P. S. ;
Goggins, T. F. ;
Mayer, I. A. ;
Brufsky, A. M. ;
Toppmeyer, D. L. ;
Kaklamani, V. G. ;
Berenberg, J. L. ;
Abrams, J. ;
Sledge, G. W., Jr. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (02) :111-121