Using Genomic Heterogeneity to Inform Therapeutic Decisions for Metastatic Colorectal Cancer: An Application of the Value of Heterogeneity Framework

被引:0
|
作者
Pataky, Reka E. [1 ,6 ]
Peacock, Stuart [1 ,2 ]
Bryan, Stirling [3 ,4 ]
Sadatsafavi, Mohsen [5 ]
Regier, Dean A. [1 ,4 ]
机构
[1] Canadian Ctr Appl Res Canc Control, BC Canc, Vancouver, BC, Canada
[2] Simon Fraser Univ, Fac Hlth Sci, Vancouver, BC, Canada
[3] Vancouver Coastal Hlth Res Inst, Ctr Clin Epidemiol & Evaluat, Vancouver, BC, Canada
[4] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada
[5] Univ British Columbia, Fac Pharmaceut Sci, Collaborat Outcomes Res & Evaluat, Vancouver, BC, Canada
[6] BC Canc Res Ctr, 675 W 10th Ave, Vancouver, BC V5Z 1L3, Canada
基金
加拿大健康研究院;
关键词
COST-EFFECTIVENESS ANALYSIS; PROPENSITY SCORE ESTIMATION; CETUXIMAB PLUS IRINOTECAN; PHASE-III TRIAL; RAS MUTATIONS; PANITUMUMAB; KRAS; BENEFIT;
D O I
10.1007/s40258-024-00926-9
中图分类号
F [经济];
学科分类号
02 ;
摘要
Background and ObjectiveMutations in KRAS and NRAS are predictive of poor response to cetuximab and panitumumab, two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies used in metastatic colorectal cancer (mCRC). Our objective was to explore the value of using KRAS and NRAS mutation status to inform third-line anti-EGFR therapy for mCRC using the value of heterogeneity (VOH) framework.MethodsWe used administrative data to identify mCRC patients who were potentially eligible for third-line therapy in 2006-2019 in British Columbia (BC), Canada. We compared three alternative stratification policies in place during the study period: the unstratified policy where anti-EGFR therapy was not offered (2006-2009), stratification by KRAS mutation (2009-2016), and stratification by KRAS+NRAS mutation (2016-2019). We used inverse-probability-of-treatment weighting to balance covariates across the three groups. Cost and survival time were calculated using a 3-year time horizon and adjusted for censoring, with bootstrapping to characterize uncertainty. Mean net monetary benefit (NMB) was calculated at a range of threshold values. The VOH of using KRAS and NRAS mutation status to inform treatment selection was calculated as the change in NMB with increasing stratification, under current (static VOH) or perfect (dynamic VOH) information.ResultsWe included 2664 patients in the analysis. At a willingness-to-pay of CA$100,000/ life-year gained (LYG), stratification on KRAS mutation status provided a static VOH of CA$1565 per patient; further stratification on KRAS+NRAS provided additional static VOH of CA$594. The static VOH exceeded the marginal cost of genomic testing under both policies.ConclusionsStratification of anti-EGFR therapy by KRAS and NRAS mutation status can provide additional value at a threshold of CA$100,000/LYG. There is diminishing marginal value and increasing marginal costs as the policy becomes more stratified. The VOH framework can illustrate the value of subgroup-specific decisions in a comprehensive way, to better inform targeted treatment policies.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] Temporospatial heterogeneity in metastatic colorectal cancer (mCRC)
    Fountzilas, C.
    Witkiewicz, A.
    Muhitch, J.
    Abrams, S.
    Knudsen, E.
    Mukherjee, S.
    Bajor, D.
    Saltzman, J.
    Wang, K.
    Iyer, R.
    Kalinski, P.
    Boland, P.
    ANNALS OF ONCOLOGY, 2020, 31 : S1458 - S1458
  • [2] Subclonal Genomic Architectures of Primary and Metastatic Colorectal Cancer Based on Intratumoral Genetic Heterogeneity
    Kim, Tae-Min
    Jung, Seung-Hyun
    An, Chang Hyeok
    Lee, Sung Hak
    Baek, In-Pyo
    Kim, Min Sung
    Park, Sung-Won
    Rhee, Je-Keun
    Lee, Sug-Hyung
    Chung, Yeun-Jun
    CLINICAL CANCER RESEARCH, 2015, 21 (19) : 4461 - 4472
  • [3] Genomic heterogeneity in metastatic colorectal cancer (CRC) demonstrated by Copy Number Variation (CNV)
    Palmer, T.
    Wood, H.
    Taylor, M.
    Fateen, W.
    Chambers, P.
    Hindley, A.
    Carr, I.
    Quirke, P.
    VIRCHOWS ARCHIV, 2014, 465 : S235 - S235
  • [4] Real-world cost-effectiveness of panel-based genomic testing to inform therapeutic decisions for metastatic colorectal cancer
    Pataky, Reka E.
    Weymann, Deirdre
    Bosdet, Ian
    Yip, Stephen
    Bryan, Stirling
    Sadatsafavi, Mohsen
    Peacock, Stuart
    Regier, Dean A.
    JOURNAL OF CANCER POLICY, 2024, 41
  • [5] Value of Information and Value of Implementation: Application of an Analytic Framework to Inform Resource Allocation Decisions in Metastatic Hormone-Refractory Prostate Cancer
    Hoomans, Ties
    Fenwick, Elisabeth A. L.
    Palmer, Steve
    Claxton, Karl
    VALUE IN HEALTH, 2009, 12 (02) : 315 - 324
  • [6] Genomic Sequencing and Insight into Clinical Heterogeneity and Prognostic Pathway Genes in Patients with Metastatic Colorectal Cancer
    Kawaguchi, Yoshikuni
    Kopetz, Scott
    Kwong, Lawrence
    Xiao, Lianchun
    Morris, Jeffrey S.
    Cao, Hop S. Tran
    Tzeng, Ching-Wei D.
    Chun, Yun Shin
    Lee, Jeffrey E.
    Vauthey, Jean-Nicolas
    JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2021, 233 (02) : 272 - +
  • [7] Metastatic heterogeneity of the consensus molecular subtypes of colorectal cancer
    Eide, Peter W.
    Moosavi, Seyed H.
    Eilertsen, Ina A.
    Brunsell, Tuva H.
    Langerud, Jonas
    Berg, Kaja C. G.
    Rosok, Bard I.
    Bjornbeth, Bjorn A.
    Nesbakken, Arild
    Lothe, Ragnhild A.
    Sveen, Anita
    NPJ GENOMIC MEDICINE, 2021, 6 (01)
  • [8] Metastatic heterogeneity of the consensus molecular subtypes of colorectal cancer
    Peter W. Eide
    Seyed H. Moosavi
    Ina A. Eilertsen
    Tuva H. Brunsell
    Jonas Langerud
    Kaja C. G. Berg
    Bård I. Røsok
    Bjørn A. Bjørnbeth
    Arild Nesbakken
    Ragnhild A. Lothe
    Anita Sveen
    npj Genomic Medicine, 6
  • [9] Tumor Heterogeneity Predicts Metastatic Potential in Colorectal Cancer
    Joung, Je-Gun
    Oh, Bo Young
    Hong, Hye Kyung
    Al-Khalidi, Hisham
    Al-Alem, Faisal
    Lee, Hae-Ock
    Bae, Joon Seol
    Kim, Jinho
    Cha, Hong-Ui
    Alotaibi, Maram
    Cho, Yong Beom
    Hassanain, Mazen
    Park, Woong-Yang
    Lee, Woo Yong
    CLINICAL CANCER RESEARCH, 2017, 23 (23) : 7209 - 7216
  • [10] Harnessing the therapeutic vulnerability of MMR heterogeneity in colorectal cancer
    Anandappa, Gayathri
    Overman, Michael J.
    CELL REPORTS MEDICINE, 2023, 4 (01)