Literature DB >> 34162659

Early Cost-effectiveness Analysis of Risk-Based Selection Strategies for Adjuvant Treatment in Stage II Colon Cancer: The Potential Value of Prognostic Molecular Markers.

Gabrielle Jongeneel1, Marjolein J E Greuter2, Natalia Kunst2,3,4,5, Felice N van Erning6, Miriam Koopman7, Jan P Medema8,9, Louis Vermeulen8,9, Jan N M Ijzermans10, Geraldine R Vink6,7, Cornelis J A Punt11, Veerle M H Coupé2.   

Abstract

BACKGROUND: To explore the potential value of consensus molecular subtypes (CMS) in stage II colon cancer treatment selection, we carried out an early cost-effectiveness assessment of a CMS-based strategy for adjuvant chemotherapy.
METHODS: We used a Markov cohort model to evaluate three selection strategies: (i) the Dutch guideline strategy (MSS+pT4), (ii) the mutation-based strategy (MSS plus a BRAF and/or KRAS mutation or MSS plus pT4), and (iii) the CMS-based strategy (CMS4 or pT4). Outcomes were number of colon cancer deaths per 1,000 patients, total discounted costs per patient (pp), and quality-adjusted life-years (QALY) pp. The analyses were conducted from a Dutch societal perspective. The robustness of model predictions was assessed in sensitivity analyses. To evaluate the value of future research, we performed a value of information (VOI) analysis.
RESULTS: The Dutch guideline strategy resulted in 8.10 QALYs pp and total costs of €23,660 pp. The CMS-based and mutation-based strategies were more effective and more costly, with 8.12 and 8.13 QALYs pp and €24,643 and €24,542 pp, respectively. Assuming a threshold of €50,000/QALY, the mutation-based strategy was considered as the optimal strategy in an incremental analysis. However, the VOI analysis showed substantial decision uncertainty driven by the molecular markers (expected value of partial perfect information: €18M).
CONCLUSIONS: On the basis of current evidence, our analyses suggest that the mutation-based selection strategy would be the best use of resources. However, the extensive decision uncertainty for the molecular markers does not allow selection of an optimal strategy at present. IMPACT: Future research is needed to eliminate decision uncertainty driven by molecular markers. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 34162659      PMCID: PMC7611620          DOI: 10.1158/1055-9965.EPI-21-0078

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.090


  44 in total

1.  Early colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.

Authors:  R Labianca; B Nordlinger; G D Beretta; S Mosconi; M Mandalà; A Cervantes; D Arnold
Journal:  Ann Oncol       Date:  2013-10       Impact factor: 32.976

2.  Clinical Outcome From Oxaliplatin Treatment in Stage II/III Colon Cancer According to Intrinsic Subtypes: Secondary Analysis of NSABP C-07/NRG Oncology Randomized Clinical Trial.

Authors:  Nan Song; Katherine L Pogue-Geile; Patrick G Gavin; Greg Yothers; S Rim Kim; Nicole L Johnson; Corey Lipchik; Carmen J Allegra; Nicholas J Petrelli; Michael J O'Connell; Norman Wolmark; Soonmyung Paik
Journal:  JAMA Oncol       Date:  2016-09-01       Impact factor: 31.777

3.  Methylation of cancer-stem-cell-associated Wnt target genes predicts poor prognosis in colorectal cancer patients.

Authors:  Felipe de Sousa E Melo; Selcuk Colak; Joyce Buikhuisen; Jan Koster; Kate Cameron; Joan H de Jong; Jurriaan B Tuynman; Pramudita R Prasetyanti; Evelyn Fessler; Saskia P van den Bergh; Hans Rodermond; Evelien Dekker; Chris M van der Loos; Steven T Pals; Marc J van de Vijver; Rogier Versteeg; Dick J Richel; Louis Vermeulen; Jan Paul Medema
Journal:  Cell Stem Cell       Date:  2011-11-04       Impact factor: 24.633

4.  Utility valuations for outcome states of colorectal cancer.

Authors:  R M Ness; A M Holmes; R Klein; R Dittus
Journal:  Am J Gastroenterol       Date:  1999-06       Impact factor: 10.864

5.  Phase III trial comparing 3-6 months of adjuvant FOLFOX4/XELOX in stage II-III colon cancer: safety and compliance in the TOSCA trial.

Authors:  S Lonardi; A Sobrero; G Rosati; M Di Bartolomeo; M Ronzoni; G Aprile; B Massida; M Scartozzi; M Banzi; M G Zampino; F Pasini; P Marchetti; M Cantore; A Zaniboni; L Rimassa; L Ciuffreda; D Ferrari; S Barni; V Zagonel; E Maiello; E Rulli; R Labianca
Journal:  Ann Oncol       Date:  2016-08-29       Impact factor: 32.976

6.  Cost-effectiveness of oxaliplatin in the adjuvant treatment of colon cancer in Canada.

Authors:  C L Attard; J A Maroun; K Alloul; D T Grima; L M Bernard
Journal:  Curr Oncol       Date:  2010-02       Impact factor: 3.677

7.  Colorectal cancer intrinsic subtypes predict chemotherapy benefit, deficient mismatch repair and epithelial-to-mesenchymal transition.

Authors:  Paul Roepman; Andreas Schlicker; Josep Tabernero; Ian Majewski; Sun Tian; Victor Moreno; Mireille H Snel; Christine M Chresta; Robert Rosenberg; Ulrich Nitsche; Teresa Macarulla; Gabriel Capella; Ramon Salazar; George Orphanides; Lodewyk F A Wessels; Rene Bernards; Iris M Simon
Journal:  Int J Cancer       Date:  2013-09-13       Impact factor: 7.396

8.  Interconnectivity between molecular subtypes and tumor stage in colorectal cancer.

Authors:  R R J Coebergh van den Braak; S Ten Hoorn; A M Sieuwerts; J B Tuynman; M Smid; S M Wilting; J W M Martens; C J A Punt; J A Foekens; J P Medema; J N M IJzermans; L Vermeulen
Journal:  BMC Cancer       Date:  2020-09-04       Impact factor: 4.430

9.  Estimating adjuvant treatment effects in Stage II colon cancer: Comparing the synthesis of randomized clinical trial data to real-world data.

Authors:  Gabrielle Jongeneel; Thomas Klausch; Felice N van Erning; Geraldine R Vink; Miriam Koopman; Cornelis J A Punt; Marjolein J E Greuter; Veerle M H Coupé
Journal:  Int J Cancer       Date:  2019-08-31       Impact factor: 7.316

10.  Transcriptional subtyping and CD8 immunohistochemistry identifies poor prognosis stage II/III colorectal cancer patients who benefit from adjuvant chemotherapy.

Authors:  W L Allen; P D Dunne; S McDade; E Scanlon; M Loughrey; H Coleman; C McCann; K McLaughlin; Z Nemeth; N Syed; P Jithesh; K Arthur; R Wilson; V Coyle; D McArt; G I Murray; L Samuel; P Nuciforo; J Jimenez; G Argiles; R Dienstmann; J Tabernero; L Messerini; S Nobili; E Mini; K Sheahan; E Ryan; P G Johnston; S Van Schaeybroeck; M Lawler; D B Longley
Journal:  JCO Precis Oncol       Date:  2018-06-13
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