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Patient relevant endpoints in oncology: current issues in the context of early benefit assessment in Germany

Author

Listed:
  • Inna Dabisch
  • Jürgen Dethling
  • Charalabos-Markos Dintsios
  • Melanie Drechsler
  • Daniel Kalanovic
  • Peter Kaskel
  • Frank Langer
  • Jörg Ruof
  • Thorsten Ruppert
  • Daniel Wirth

Abstract

D61; H51; I18. Copyright Dabisch et al.; licensee Springer. 2014

Suggested Citation

  • Inna Dabisch & Jürgen Dethling & Charalabos-Markos Dintsios & Melanie Drechsler & Daniel Kalanovic & Peter Kaskel & Frank Langer & Jörg Ruof & Thorsten Ruppert & Daniel Wirth, 2014. "Patient relevant endpoints in oncology: current issues in the context of early benefit assessment in Germany," Health Economics Review, Springer, vol. 4(1), pages 1-8, December.
    • Handle: RePEc:spr:hecrev:v:4:y:2014:i:1:p:1-8:10.1186/2191-1991-4-2
    DOI: 10.1186/2191-1991-4-2
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    References listed on IDEAS

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    1. Mathews, Holly F. & Lannin, Donald R. & Mitchell, James P., 1994. "Coming to terms with advanced breast cancer: Black women's narratives from Eastern North Carolina," Social Science & Medicine, Elsevier, vol. 38(6), pages 789-800, March.
    Full references (including those not matched with items on IDEAS)

    Citations

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    Cited by:

    1. Niehaus, Ines & Dintsios, Charalabos-Markos, 2018. "Confirmatory versus explorative endpoint analysis: Decision-making on the basis of evidence available from market authorization and early benefit assessment for oncology drugs," Health Policy, Elsevier, vol. 122(6), pages 599-606.
    2. Ingo Stiller & Arjen Witteloostuijn & Bart Cambré, 2021. "Do current radical innovation measures actually measure radical drug innovation?," Scientometrics, Springer;Akadémiai Kiadó, vol. 126(2), pages 1049-1078, February.
    3. Jörg Ruof & Thomas Staab & Charalabos-Markos Dintsios & Jakob Schröter & Friedrich Wilhelm Schwartz, 2016. "Comparison of post-authorisation measures from regulatory authorities with additional evidence requirements from the HTA body in Germany – are additional data requirements by the Federal Joint Committ," Health Economics Review, Springer, vol. 6(1), pages 1-11, December.
    4. C. M. Dintsios & I. Beinhauer, 2020. "The impact of additive or substitutive clinical study design on the negotiated reimbursement for oncology pharmaceuticals after early benefit assessment in Germany," Health Economics Review, Springer, vol. 10(1), pages 1-25, December.
    5. Ruof, Jörg & Knoerzer, Dietrich & Dünne, Anja-Alexandra & Dintsios, Charalabos-Markos & Staab, Thomas & Schwartz, Friedrich Wilhelm, 2014. "Analysis of endpoints used in marketing authorisations versus value assessments of oncology medicines in Germany," Health Policy, Elsevier, vol. 118(2), pages 242-254.

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    More about this item

    Keywords

    AMNOG; German health care reform; Oncology; Endpoints; Progression-free survival; Patient-relevant benefit;
    All these keywords.

    JEL classification:

    • D61 - Microeconomics - - Welfare Economics - - - Allocative Efficiency; Cost-Benefit Analysis
    • H51 - Public Economics - - National Government Expenditures and Related Policies - - - Government Expenditures and Health
    • I18 - Health, Education, and Welfare - - Health - - - Government Policy; Regulation; Public Health

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