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Reply to Paulo Schiavom DuarteJulian M. M. Rogasch

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https://doi.org/10.1007/s00259-021-05469-y LETTER TO THE EDITOR

Reply to Paulo Schiavom Duarte

Julian M. M. Rogasch1,2 · Carsten Kobe3

Received: 15 June 2021 / Accepted: 16 June 2021

© The Author(s) 2021

Dear Sir,

We thank Paulo Duarte for his interest and appreciate his comments regarding our review “Moving the goalposts while scoring―the dilemma posed by new PET technologies.”

The aim of our review was to highlight the clinical impact of new technologies for positron emission tomography (PET). We agree with Paulo Duarte that not every clinical aspect of a diagnostic tool such as PET or of new technolo- gies developed for this modality require the same degree of clinical evidence as that outlined by Fryback and Thornbury [1] and demanded for therapeutic drugs. However, when it comes to technical innovations in the field of PET as an existing imaging modality, we as a nuclear medicine com- munity should not be content simply with possible improve- ments in certain aspects of image quality or lesion detect- ability. If there are considerable benefits associated with new PET technologies, they should ultimately be of demonstrable value for patient care and patient-relevant outcomes.

We also agree with our colleague that the definition of benefit for the patient may vary between different clinical settings. In this regard, a benefit would not be restricted to prognosis (survival) but might be manifested in an ear- lier diagnosis of relapse (if this is advantageous to the

treatment), higher lesion detection rates (if this results in relevant treatment changes), or even in a reduction of the administered activity and radiation exposure.

Paulo Duarte further suggests that diagnosis and prog- nosis of a disease have a value of their own. We have con- vincing data showing that the use of PET is beneficial for patients and can improve patient survival in several settings.

In contrast, there is a lack of evidence for further improve- ment with “new PET technologies.” The mere observa- tion that new PET technologies might have clinical con- sequences suggests that they should not be used without careful thought. Although this may appear overly cautious, such caution is warranted as it could prevent potential disad- vantageous effects, and it is especially important in clinical scenarios in which treatment decisions are influenced by variations in image characteristics. The potentially higher lesion detection rates associated with the new PET tech- nologies are also a concern. In this regard, one prominent and painful example of clinical problems resulting from the transition to new technologies was with PET in lymphoma, where the original introduction of PET had allowed us to omit radiotherapy in many patients, but the percentage of patients undergoing radiotherapy rebounded on stepwise introduction of emerging PET technologies.

This is why we support all efforts to ensure imaging com- parability, as put forward by the EARL initiative, and we rec- ommend being adequately cautious and continuously aware of the possible clinical impact of new PET technologies.

Best regards,

Julian Rogasch and Carsten Kobe.

Acknowledgements JMMR is a participant in the BIH-Charité Digital Clinician Scientist Program funded by the Charité – Universitätsmedi- zin Berlin, the Berlin Institute of Health, and the German Research Foundation (DFG).

This article is part of the Topical Collection on Letter to the Editor

* Julian M. M. Rogasch julian.rogasch@charite.de

1 Department of Nuclear Medicine, Charité –

Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1, D-13353 Berlin, Germany

2 Berlin Institute of Health (BIH), Berlin, Germany

3 Department of Nuclear Medicine, University Hospital of Cologne, Cologne, Germany

/ Published online: 22 June 2021 European Journal of Nuclear Medicine and Molecular Imaging (2021) 48:3024–3025

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Funding Open Access funding enabled and organized by Projekt DEAL.

Declarations

Ethics approval This article does not contain any studies with human participants or animals performed by any of the authors.

Conflict of interest The authors declare no competing interests.

Open Access This article is licensed under a Creative Commons Attri- bution 4.0 International License, which permits use, sharing, adapta- tion, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated

otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.

Reference

1. Fryback DG, Thornbury JR. The efficacy of diagnostic imaging.

Med Decis Making. 1991;11:88–94. https:// doi. org/ 10. 1177/

02729 89x91 01100 203.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

3025 European Journal of Nuclear Medicine and Molecular Imaging (2021) 48:3024–3025

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