Estimated Cost of Anticancer Therapy Directed by Comprehensive Genomic Profiling in a Single-Center Study

被引:29
作者
Chawla, Anita [1 ]
Janku, Filip [3 ]
Wheler, Jennifer J. [3 ]
Miller, Vincent A. [2 ]
Ryan, Jason [2 ]
Anhorn, Rachel [2 ]
Zhou, Zhou [1 ]
Signorovitch, James [1 ]
机构
[1] Anal Grp, 1010 El Camino Real,Suite 310, Menlo Pk, CA 94025 USA
[2] Fdn Med, Cambridge, MA USA
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
CELL LUNG-CANCER; PERSONALIZED MEDICINE; PRECISION MEDICINE; VALIDATION; IMPACT; ACTIONABILITY; ONCOLOGY; OUTCOMES; PROGRAM; TARGETS;
D O I
10.1200/PO.18.00074
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Comprehensive genomic profiling (CGP) detects several classes of genomic alterations across numerous genes simultaneously and can match more patients with genomically targeted therapies than conventional molecular profiling. The current study estimated the costs of anticancer drugs and overall survival (OS) for patients who were treated with matched and unmatched therapy. Methods Costs were estimated for patients with complete data (188 of 500 patients) from a prospective, nonrandomized study of patients with diverse refractory cancers who underwent CGP and were treated with matched or unmatched therapy. We assessed mean time to treatment failure (TTF) and mean observed OS. Patient-specific drug and administration costs were imputed for the first regimen after CGP on the basis of drug classes, unit costs, and time on treatment. Results Patients on matched (n = 122) versus unmatched (n = 66) therapy had longer mean TTF (+1.5 months) and observed OS (+2.4 months) and higher drug costs (+$38,065; all P < .01). Increased drug costs were largely attributable to the longer duration of therapy associated with extended TTF (66.3%) rather than higher monthly drug costs (33.7%). Incremental increases in TTF (+1.9 months v +1.2 months) and observed OS (+2.5 months v +2.1 months) between matched and unmatched therapies were larger for those who underwent CGP in earlier- versus later-line therapy. Incremental increases in drug costs between matched and unmatched therapies were lower for earlier- compared with later-line therapy (+$27,000 v +$43,000, respectively). Conclusion Matched therapy was associated with longer TTF, increased OS, and manageable incremental cost increases compared with unmatched therapy. Most of these increased costs were a result of the longer duration of therapy rather than higher monthly drug costs. The benefits of matching were numerically greater in earlier versus later lines of therapy, which is consistent with the value of early use of CGP. (C) 2018 by American Society of Clinical Oncology Licensed under the Creative Commons Attribution 4.0 License
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页码:1 / 11
页数:12
相关论文
共 30 条
  • [1] [Anonymous], 2018, NCCN Clinical Practice Guidelines in Oncology, DOI DOI 10.1016/B978-0-323-35762-3.00092-5
  • [2] Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT) A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology
    Cheng, Donavan T.
    Mitchell, Talia N.
    Zehir, Ahmet
    Shah, Ronak H.
    Benayed, Ryma
    Syed, Aijazuddin
    Chandramohan, Raghu
    Liu, Zhen Yu
    Won, Helen H.
    Scott, Sasinya N.
    Brannon, A. Rose
    O'Reilly, Catherine
    Sadowska, Justyna
    Casanova, Jacklyn
    Yannes, Angela
    Hechtman, Jaclyn F.
    Yao, Jinjuan
    Song, Wei
    Ross, Dara S.
    Oultache, Alifya
    Dogan, Snjezana
    Borsu, Laetitia
    Hameed, Meera
    Nafa, Khedoudja
    Arcila, Maria E.
    Ladanyi, Marc
    Berger, Michael F.
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (03) : 251 - 264
  • [3] Impact of genomic profiling on the treatment and outcomes of patients with advanced gastrointestinal malignancies
    Dhir, Mashaal
    Choudry, Haroon A.
    Holtzman, Matthew P.
    Pingpank, James F.
    Ahrendt, Steven A.
    Zureikat, Amer H.
    Hogg, Melissa E.
    Bartlett, David L.
    Zeh, Herbert J.
    Singhi, Aatur D.
    Bahary, Nathan
    [J]. CANCER MEDICINE, 2017, 6 (01): : 195 - 206
  • [4] Broad, Hybrid Capture-Based Next-Generation Sequencing Identifies Actionable Genomic Alterations in Lung Adenocarcinomas Otherwise Negative for Such Alterations by Other Genomic Testing Approaches
    Drilon, Alexander
    Wang, Lu
    Arcila, Maria E.
    Balasubramanian, Sohail
    Greenbowe, Joel R.
    Ross, Jeffrey S.
    Stephens, Phil
    Lipson, Doron
    Miller, Vincent A.
    Kris, Mark G.
    Ladanyi, Marc
    Rizvi, Naiyer A.
    [J]. CLINICAL CANCER RESEARCH, 2015, 21 (16) : 3631 - 3639
  • [5] Impact of a Biomarker-Based Strategy on Oncology Drug Development: A Meta-Analysis of Clinical Trials Leading to FDA Approval
    Fontes Jardim, Denis L.
    Schwaederle, Maria
    Wei, Caimiao
    Lee, J. Jack
    Hong, David S.
    Eggermont, Alexander M.
    Schilsky, Richard L.
    Mendelsohn, John
    Lazar, Vladimir
    Kurzrock, Razelle
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (11):
  • [6] Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing
    Frampton, Garrett M.
    Fichtenholtz, Alex
    Otto, Geoff A.
    Wang, Kai
    Downing, Sean R.
    He, Jie
    Schnall-Levin, Michael
    White, Jared
    Sanford, Eric M.
    An, Peter
    Sun, James
    Juhn, Frank
    Brennan, Kristina
    Iwanik, Kiel
    Maillet, Ashley
    Buell, Jamie
    White, Emily
    Zhao, Mandy
    Balasubramanian, Sohail
    Terzic, Selmira
    Richards, Tina
    Banning, Vera
    Garcia, Lazaro
    Mahoney, Kristen
    Zwirko, Zac
    Donahue, Amy
    Beltran, Himisha
    Mosquera, Juan Miguel
    Rubin, Mark A.
    Dogan, Snjezana
    Hedvat, Cyrus V.
    Berger, Michael F.
    Pusztai, Lajos
    Lechner, Matthias
    Boshoff, Chris
    Jarosz, Mirna
    Vietz, Christine
    Parker, Alex
    Miller, Vincent A.
    Ross, Jeffrey S.
    Curran, John
    Cronin, Maureen T.
    Stephens, Philip J.
    Lipson, Doron
    Yelensky, Roman
    [J]. NATURE BIOTECHNOLOGY, 2013, 31 (11) : 1023 - +
  • [7] Tumor Mutational Burden as an Independent Predictor of Response to Immunotherapy in Diverse Cancers
    Goodman, Aaron M.
    Kato, Shumei
    Bazhenova, Lyudmila
    Patel, Sandip P.
    Frampton, Garrett M.
    Miller, Vincent
    Stephens, Philip J.
    Daniels, Gregory A.
    Kurzrock, Razelle
    [J]. MOLECULAR CANCER THERAPEUTICS, 2017, 16 (11) : 2598 - 2608
  • [8] Genomic Profiling of Advanced Non-Small Cell Lung Cancer in Community Settings: Gaps and Opportunities
    Gutierrez, Martin E.
    Choi, Kelly
    Lanman, Richard B.
    Licitra, Edward J.
    Skrzypczak, Stanley M.
    Benito, Ruth Pe
    Wu, Tommy
    Arunajadai, Srikesh
    Kaur, Sukhi
    Harper, Harry
    Pecora, Andrew L.
    Schultz, Eric V.
    Goldberg, Stuart L.
    [J]. CLINICAL LUNG CANCER, 2017, 18 (06) : 651 - 659
  • [9] Cost Effectiveness of Personalized Therapy for First-Line Treatment of Stage IV and Recurrent Incurable Adenocarcinoma of the Lung
    Handorf, Elizabeth A.
    McElligott, Sean
    Vachani, Anil
    Langer, Corey J.
    Bristol Demeter, Mirar
    Armstrong, Katrina
    Asch, David A.
    [J]. JOURNAL OF ONCOLOGY PRACTICE, 2012, 8 (05) : 267 - +
  • [10] A Retrospective Analysis of Precision Medicine Outcomes in Patients With Advanced Cancer Reveals Improved Progression-Free Survival Without Increased Health Care Costs
    Haslem, Derrick S.
    Van Norman, S. Burke
    Fulde, Gail
    Knighton, Andrew J.
    Belnap, Tom
    Butler, Allison M.
    Rhagunath, Sharanya
    Newman, David
    Gilbert, Heather
    Tudor, Brian P.
    Lin, Karen
    Stone, Gary R.
    Loughmiller, David L.
    Mishra, Pravin J.
    Srivastava, Rajendu
    Ford, James M.
    Nadauld, Lincoln D.
    [J]. JOURNAL OF ONCOLOGY PRACTICE, 2017, 13 (02) : E108 - E119