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. 2022 Apr;49(5):1682-1699.
doi: 10.1007/s00259-021-05600-z. Epub 2022 Feb 11.

EANM procedure guideline for the treatment of liver cancer and liver metastases with intra-arterial radioactive compounds

Affiliations

EANM procedure guideline for the treatment of liver cancer and liver metastases with intra-arterial radioactive compounds

M Weber et al. Eur J Nucl Med Mol Imaging. 2022 Apr.

Abstract

Primary liver tumours (i.e. hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (ICC)) are among the most frequent cancers worldwide. However, only 10-20% of patients are amenable to curative treatment, such as resection or transplant. Liver metastases are most frequently caused by colorectal cancer, which accounts for the second most cancer-related deaths in Europe. In both primary and secondary tumours, radioembolization has been shown to be a safe and effective treatment option. The vast potential of personalized dosimetry has also been shown, resulting in markedly increased response rates and overall survival. In a rapidly evolving therapeutic landscape, the role of radioembolization will be subject to changes. Therefore, the decision for radioembolization should be taken by a multidisciplinary tumour board in accordance with the current clinical guidelines. The purpose of this procedure guideline is to assist the nuclear medicine physician in treating and managing patients undergoing radioembolization treatment. PREAMBLE: The European Association of Nuclear Medicine (EANM) is a professional non-profit medical association that facilitates communication worldwide among individuals pursuing clinical and research excellence in nuclear medicine. The EANM was founded in 1985. These guidelines are intended to assist practitioners in providing appropriate nuclear medicine care for patients. They are not inflexible rules or requirements of practice and are not intended, nor should they be used, to establish a legal standard of care. The ultimate judgment regarding the propriety of any specific procedure or course of action must be made by medical professionals taking into account the unique circumstances of each case. Thus, there is no implication that an approach differing from the guidelines, standing alone, is below the standard of care. To the contrary, a conscientious practitioner may responsibly adopt a course of action different from that set out in the guidelines when, in the reasonable judgment of the practitioner, such course of action is indicated by the condition of the patient, limitations of available resources or advances in knowledge or technology subsequent to publication of the guidelines. The practice of medicine involves not only the science but also the art of dealing with the prevention, diagnosis, alleviation and treatment of disease. The variety and complexity of human conditions make it impossible to always reach the most appropriate diagnosis or to predict with certainty a particular response to treatment. Therefore, it should be recognised that adherence to these guidelines will not ensure an accurate diagnosis or a successful outcome. All that should be expected is that the practitioner will follow a reasonable course of action based on current knowledge, available resources and the needs of the patient to deliver effective and safe medical care. The sole purpose of these guidelines is to assist practitioners in achieving this objective.

Keywords: 166Ho-microspheres; 90Y-microspheres; Dosimetry; Glass microspheres; Guidelines; Liver cancer; Nuclear medicine; QuiremSpheres®; Resin microspheres; SIR-spheres®; TheraSphere®.

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Conflict of interest statement

M. Weber holds/held consulting roles for Boston Scientific, Terumo, and Lilly. M. Lam is a consultant and received research support from Terumo and Boston Scientific. UMC Utrecht receives royalty payments from Terumo. C. Chiesa has been a consultant for Boston Scientific and TERUMO for guideline development and congress symposia. He received a research grant in 2018 from Boston Scientific.

P. Flamen reports advisory board and consultancy fees for SIRTEX. L. Bodei reports non-remunerated consultant/speaker roles for AAA-Novartis, ITG, Iba, Clovis Oncology, and MTTI and research grants by AAA-Novartis.

E. Garin is a consultant for Boston Scientific (1 grant for DOSISPHERE trial, personal fees). K. Herrmann reports personal fees from Bayer, personal fees and other from Sofie Biosciences, personal fees from SIRTEX, non-financial support from ABX, personal fees from Adacap, personal fees from Curium, personal fees from Endocyte, grants and personal fees from BTG, personal fees from IPSEN, personal fees from Siemens Healthineers, personal fees from GE Healthcare, personal fees from Amgen, personal fees from Novartis, personal fees from ymabs, personal fees from Aktis Oncology, personal fees from Theragnostics, and personal fees from Pharma15, outside the submitted work.

M. Konijnenberg, M. Lustre, M. Cremonesi, S. Gnesin, and T. Kracmerova have nothing to disclose.

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