<?xml version="1.0" encoding="utf-8" standalone="yes" ?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
  <channel>
    <title>Carlo Chiesa | Theragnostic Imaging</title>
    <link>https://www.theragnostics.no/en/author/carlo-chiesa/</link>
      <atom:link href="https://www.theragnostics.no/en/author/carlo-chiesa/index.xml" rel="self" type="application/rss+xml" />
    <description>Carlo Chiesa</description>
    <generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Fri, 01 Dec 2023 00:00:00 +0000</lastBuildDate>
    <image>
      <url>https://www.theragnostics.no/media/icon_hu14557955862192370321.png</url>
      <title>Carlo Chiesa</title>
      <link>https://www.theragnostics.no/en/author/carlo-chiesa/</link>
    </image>
    
    <item>
      <title>EFOMP policy statement NO. 19: Dosimetry in nuclear medicine therapy - Molecular radiotherapy</title>
      <link>https://www.theragnostics.no/en/publications/sjogreen-gleisner-2023-efomp/</link>
      <pubDate>Fri, 01 Dec 2023 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/sjogreen-gleisner-2023-efomp/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;The European Council Directive 2013/59/Euratom (BSS Directive) includes optimisation of treatment with radiotherapeutic procedures based on patient dosimetry and verification of the absorbed doses delivered. The present policy statement summarises aspects of three directives relating to the therapeutic use of radiopharmaceuticals and medical devices, and outlines the steps needed for implementation of patient dosimetry for radioactive drugs. To support the transition from administrations of fixed activities to personalised treatments based on patient-specific dosimetry, EFOMP presents a number of recommendations including: increased networking between centres and disciplines to support data collection and development of codes-of-practice; resourcing to support an infrastructure that permits routine patient dosimetry; research funding to support investigation into individualised treatments; inter-disciplinary training and education programmes; and support for investigator led clinical trials. Close collaborations between the medical physicist and responsible practitioner are encouraged to develop a similar pathway as is routine for external beam radiotherapy and brachytherapy. EFOMP&amp;rsquo;s policy is to promote the roles and responsibilities of medical physics throughout Europe in the development of molecular radiotherapy to ensure patient benefit. As the BSS directive is adopted throughout Europe, unprecedented opportunities arise to develop informed treatments that will mitigate the risks of under- or over-treatments.&lt;/p&gt;
</description>
    </item>
    
    <item>
      <title>Results from an EANM survey on time estimates and personnel responsible for main tasks in molecular radiotherapy dosimetry</title>
      <link>https://www.theragnostics.no/en/publications/gabina-2023-results/</link>
      <pubDate>Sat, 01 Jul 2023 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/gabina-2023-results/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;No abstract available&lt;/p&gt;
</description>
    </item>
    
    <item>
      <title>EANM dosimetry committee series on standard operational procedures: a unified methodology for 99mTc-MAA pre- and 90Y peri-therapy dosimetry in liver radioembolization with 90Y microspheres</title>
      <link>https://www.theragnostics.no/en/publications/chiesa-2021-eanm/</link>
      <pubDate>Fri, 12 Nov 2021 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/chiesa-2021-eanm/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;The aim of this standard operational procedure is to standardize the methodology employed for the evaluation of pre- and post-treatment absorbed dose calculations in &lt;sup&gt;90&lt;/sup&gt;Y microsphere liver radioembolization. Basic assumptions include the permanent trapping of microspheres, the local energy deposition method for voxel dosimetry, and the patient-relative calibration method for activity quantification.The identity of &lt;sup&gt;99m&lt;/sup&gt;Tc albumin macro-aggregates (MAA) and &lt;sup&gt;90&lt;/sup&gt;Y microsphere biodistribution is also assumed. The large observed discrepancies in some patients between &lt;sup&gt;99m&lt;/sup&gt;Tc-MAA predictions and actual &lt;sup&gt;90&lt;/sup&gt;Y microsphere distributions for lesions is discussed. Absorbed dose predictions to whole non-tumoural liver are considered more reliable and the basic predictors of toxicity. Treatment planning based on mean absorbed dose delivered to the whole non-tumoural liver is advised, except in super-selective treatments.Given the potential mismatch between MAA simulation and actual therapy, absorbed doses should be calculated both pre- and post-therapy. Distinct evaluation between target tumours and non-tumoural tissue, including lungs in cases of lung shunt, are vital for proper optimization of therapy. Dosimetry should be performed first according to a mean absorbed dose approach, with an optional, but important, voxel level evaluation. Fully corrected &lt;sup&gt;99m&lt;/sup&gt;Tc-MAA Single Photon Emission Computed Tomography (SPECT)/computed tomography (CT) and &lt;sup&gt;90&lt;/sup&gt;Y TOF PET/CT are regarded as optimal acquisition methodologies, but, for institutes where SPECT/CT is not available, non-attenuation corrected &lt;sup&gt;99m&lt;/sup&gt;Tc-MAA SPECT may be used. This offers better planning quality than non dosimetric methods such as Body Surface Area (BSA) or mono-compartmental dosimetry. Quantitative &lt;sup&gt;90&lt;/sup&gt;Y bremsstrahlung SPECT can be used if dedicated correction methods are available.The proposed methodology is feasible with standard camera software and a spreadsheet. Available commercial or free software can help facilitate the process and improve calculation time.&lt;/p&gt;
</description>
    </item>
    
    <item>
      <title>EANM Dosimetry Committee series on standard operational procedures for internal dosimetry for 131I mIBG treatment of neuroendocrine tumours</title>
      <link>https://www.theragnostics.no/en/publications/gear-2020-eanm/</link>
      <pubDate>Fri, 06 Mar 2020 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/gear-2020-eanm/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;The purpose of the EANM Dosimetry Committee Series on &amp;quot;Standard Operational Procedures for Dosimetry&amp;quot; (SOP) is to provide advice to scientists and clinicians on how to perform patient-specific absorbed dose assessments. This SOP describes image and data acquisition parameters and dosimetry calculations to determine the absorbed doses delivered to whole-body, tumour and normal organs following a therapeutic administration of &lt;sup&gt;131&lt;/sup&gt;I mIBG for the treatment of neuroblastoma or adult neuroendocrine tumours. Recommendations are based on evidence in recent literature where available and on expert opinion within the community. This SOP is intended to promote standardisation of practice within the community and as such is based on the facilities and expertise that should be available to any centre able to perform specialised treatments with radiopharmaceuticals and patient-specific dosimetry. A clinical example is given to demonstrate the application of the absorbed dose calculations.&lt;/p&gt;
</description>
    </item>
    
    <item>
      <title>Re: Tumor Targeting and Three-Dimensional Voxel-Based Dosimetry to Predict Tumor Response, Toxicity, and Survival after Yttrium-90 Resin Microsphere Radioembolization in Hepatocellular Carcinoma</title>
      <link>https://www.theragnostics.no/en/publications/walrand-2019-re-/</link>
      <pubDate>Sun, 01 Dec 2019 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/walrand-2019-re-/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;No abstract available&lt;/p&gt;
</description>
    </item>
    
    <item>
      <title>Dosimetry-based treatment planning for molecular radiotherapy: a summary of the 2017 report from the Internal Dosimetry Task Force</title>
      <link>https://www.theragnostics.no/en/publications/stokke-2017-dosimetry-based/</link>
      <pubDate>Tue, 21 Nov 2017 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/stokke-2017-dosimetry-based/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;The European directive on basic safety standards (Council directive 2013/59 Euratom) mandates dosimetry-based treatment planning for radiopharmaceutical therapies. The directive comes into operation February 2018, and the aim of a report produced by the Internal Dosimetry Task Force of the European Association of Nuclear Medicine is to address this aspect of the directive. A summary of the report is presented. A brief review of five of the most common therapy procedures is included in the current text, focused on the potential to perform patient-specific dosimetry. In the full report, 11 different therapeutic procedures are included, allowing additional considerations of effectiveness, references to specific literature on quantitative imaging and dosimetry, and existing evidence for absorbed dose-effect correlations for each treatment. Individualized treatment planning with tracer diagnostics and verification of the absorbed doses delivered following therapy is found to be scientifically feasible for almost all procedures investigated, using quantitative imaging and/or external monitoring. Translation of this directive into clinical practice will have significant implications for resource requirements. Molecular radiotherapy is undergoing a significant expansion, and the groundwork for dosimetry-based treatment planning is already in place. The mandated individualization is likely to improve the effectiveness of the treatments, although must be adequately resourced.&lt;/p&gt;
</description>
    </item>
    
  </channel>
</rss>
