Literature DB >> 29998292

Economic Analysis of a Noninvasive Molecular Pathologic Assay for Pigmented Skin Lesions.

John Hornberger1,2, Daniel M Siegel3,4.   

Abstract

Importance: A recently described noninvasive gene expression test (the pigmented lesion assay [PLA]) with adhesive patch-based sampling has the potential to rule out melanoma and the need for surgical biopsy of pigmented lesions suggestive of melanoma with a negative predictive value of 99% compared with 83% for the histopathologic standard of care. The cost implications of using this molecular test vs visual assessment followed by biopsy and histopathologic assessment (VAH) have not been evaluated. Objective: To determine potential cost savings of PLA use vs the VAH pathway. Design, Setting, and Participants: This health economic analysis performed from a US payer perspective was based on consensus treatment guidelines and fee schedules from the Centers for Medicare & Medicaid Services. Data for model input were derived from routine use of the test in US dermatology practices and literature. Participants included patients with primary cutaneous pigmented lesions suggestive of melanoma. Data were analyzed from February 8 to December 1, 2017. Main Outcomes and Measures: The primary analysis consisted of the relative reduction in costs of diagnostic surgical procedures for PLA vs VAH management. Additional analyses included stage-related treatment costs associated with delays in diagnosis.
Results: In the cost analysis for this economic model, the relative reduction in surgical procedure costs (biopsy and subsequent excision), assuming $0 for the PLA to facilitate multiple comparison scenarios, was -$395 compared with VAH. The relative reduction in stage-related treatment costs associated with the PLA was -$433 compared with VAH, primarily associated with avoidance of delays due to false-negative diagnoses. Surveillance costs were reduced by -$119 with the PLA. The total cost of fully adjudicating a lesion suggestive of melanoma by VAH was $947. At a mean selling price reference point for PLA of $500, cost savings of $447 (47%) per lesion tested could be realized. Conclusions and Relevance: The results of this analysis suggest that the PLA reduces cost and may improve the care of patients with primary pigmented skin lesions suggestive of melanoma.

Entities:  

Mesh:

Year:  2018        PMID: 29998292      PMCID: PMC6143039          DOI: 10.1001/jamadermatol.2018.1764

Source DB:  PubMed          Journal:  JAMA Dermatol        ISSN: 2168-6068            Impact factor:   10.282


  39 in total

1.  Clinical decision making based on histopathologic grading and margin status of dysplastic nevi.

Authors:  Keith L Duffy; David J Mann; Vesna Petronic-Rosic; Christopher R Shea
Journal:  Arch Dermatol       Date:  2012-02

2.  Melanoma quality of life: pilot study using utility measurements.

Authors:  Sallyann M Coleman King; Paola Bonaccorsi; Sandy Bendeck; Jason Hadley; Katherine Puttgen; Paul G Kolm; Emir Veledar; David Lawson; Suephy C Chen
Journal:  Arch Dermatol       Date:  2010-11-15

3.  Degree of clinical concern and dysplasia affect biopsy technique and management of dysplastic nevi with positive biopsy margins: Results from a survey of New England dermatologists.

Authors:  Lana X Tong; Peggy A Wu; Caroline C Kim
Journal:  J Am Acad Dermatol       Date:  2016-02       Impact factor: 11.527

4.  The epidemiology of nevi and signs of skin aging in the adult general population: Results of the KORA-survey 2000.

Authors:  Torsten Schäfer; Jessica Merkl; Eckart Klemm; Heinz-Erich Wichmann; Johannes Ring
Journal:  J Invest Dermatol       Date:  2006-04-27       Impact factor: 8.551

5.  Utility of a Noninvasive 2-Gene Molecular Assay for Cutaneous Melanoma and Effect on the Decision to Biopsy.

Authors:  Laura K Ferris; Burkhard Jansen; Jonhan Ho; Klaus J Busam; Kenneth Gross; Doyle D Hansen; John P Alsobrook; Zuxu Yao; Gary L Peck; Pedram Gerami
Journal:  JAMA Dermatol       Date:  2017-07-01       Impact factor: 10.282

6.  The performance of MelaFind: a prospective multicenter study.

Authors:  Gary Monheit; Armand B Cognetta; Laura Ferris; Harold Rabinovitz; Kenneth Gross; Mary Martini; James M Grichnik; Martin Mihm; Victor G Prieto; Paul Googe; Roy King; Alicia Toledano; Nikolai Kabelev; Maciej Wojton; Dina Gutkowicz-Krusin
Journal:  Arch Dermatol       Date:  2010-10-18

7.  Effect of biopsy type on outcomes in the treatment of primary cutaneous melanoma.

Authors:  Jane K Mills; Ian White; Brian Diggs; Jeanine Fortino; John T Vetto
Journal:  Am J Surg       Date:  2013-05       Impact factor: 2.565

8.  Atypical (dysplastic) nevi: outcomes of surgical excision and association with melanoma.

Authors:  Kavitha K Reddy; Michele J Farber; Jag Bhawan; Roy G Geronemus; Gary S Rogers
Journal:  JAMA Dermatol       Date:  2013-08       Impact factor: 10.282

9.  Determination of the impact of melanoma surgical timing on survival using the National Cancer Database.

Authors:  Ruzica Z Conic; Claudia I Cabrera; Alok A Khorana; Brian R Gastman
Journal:  J Am Acad Dermatol       Date:  2017-10-17       Impact factor: 11.527

10.  Accuracy of diagnostic biopsy for cutaneous melanoma: implications for surgical oncologists.

Authors:  Tina J Hieken; Roberto Hernández-Irizarry; Julia M Boll; Jamie E Jones Coleman
Journal:  Int J Surg Oncol       Date:  2013-09-11
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  5 in total

1.  Real-World Application of a Noninvasive Two-Gene Expression Test for Melanoma Diagnosis.

Authors:  Michael A Marchetti; Japbani K Nanda; Silvia E Mancebo; Stephen W Dusza
Journal:  J Invest Dermatol       Date:  2021-03-17       Impact factor: 7.590

2.  Use of the Pigmented Lesion Assay to rapidly screen a patient with numerous clinically atypical pigmented lesions.

Authors:  Aatman Shah; John Hyngstrom; Scott R Florell; Douglas Grossman
Journal:  JAAD Case Rep       Date:  2019-11-20

3.  Detection of cutaneous malignant melanoma using RNA sampled by tape strips: A study protocol.

Authors:  Ida M Heerfordt; Jeppe D Andersen; Peter A Philipsen; Linnea Langhans; Torben Tvedebrink; Grethe Schmidt; Thomas Poulsen; Catharina M Lerche; Niels Morling; Hans Christian Wulf
Journal:  PLoS One       Date:  2022-09-21       Impact factor: 3.752

4.  Pigmented Lesion Assay for Suspected Melanoma Lesions: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2021-06-04

5.  Response to Rigel et al.

Authors:  Michael A Marchetti; Stephen W Dusza
Journal:  J Invest Dermatol       Date:  2021-07-14       Impact factor: 8.551

  5 in total

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