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PRRT: identikit of the perfect patient.
Albertelli, M; Dotto, A; Di Dato, C; Malandrino, P; Modica, R; Versari, A; Colao, A; Ferone, D; Faggiano, A.
Afiliação
  • Albertelli M; Endocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Dotto A; Endocrinology Unit, Department of Internal Medicine and Medical Specialties (DiMI) and Center of Excellence for Biomedical Research, University of Genova, Genova, Italy.
  • Di Dato C; Endocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Malandrino P; Endocrinology Unit, Department of Internal Medicine and Medical Specialties (DiMI) and Center of Excellence for Biomedical Research, University of Genova, Genova, Italy.
  • Modica R; Endocrinology, Department of Experimental Medicine, "Sapienza", University of Rome, Rome, Italy.
  • Versari A; Endocrinology, Department of Clinical and Experimental Medicine, Garibaldi-Nesima Medical Center, University of Catania, Catania, Italy.
  • Colao A; Endocrinology, Department of Clinical Medicine and Surgery, "Federico II" University of Napoli, Napoli, Italy.
  • Ferone D; Nuclear Medicine, Azienda Ospedaliera Santa Maria Nuova-IRCCS Reggio Emilia, Reggio Emilia, Italy.
  • Faggiano A; Endocrinology, Department of Clinical Medicine and Surgery, "Federico II" University of Napoli, Napoli, Italy.
Rev Endocr Metab Disord ; 22(3): 563-579, 2021 09.
Article em En | MEDLINE | ID: mdl-32978685
ABSTRACT
Peptide receptor radionuclide therapy (PRRT) has been strengthened since the publication of NETTER-1. Nevertheless, the correct positioning in the therapeutic algorithm is debated, and no optimal sequence has yet been standardized. Possible criteria to predict the response to PRRT in neuroendocrine tumors (NET) have been proposed. The aim of this review is to define the perfect identity of the eligible patient who can mostly benefit from this therapy. Possible predictive criteria which have been analysed were primary tumor site, grading, tumor burden, FDG PET and 68Ga-PET uptake. Primary tumor site and 68Ga-PET uptake do not play a pivotal role in predicting the response, while tumor burden, FDG PET uptake and grading seem to represent predictive/prognostic factors for response to PRRT. The heterogeneity in trial designs, patient populations, type of radionuclides, previous therapies and measurement of outcomes, inevitably limits the strength of our conclusions, therefore care must be taken in applying these results to clinical practice. In conclusion, the perfect patient, selected by 68Ga-PET uptake, will likely have a relatively limited liver tumor burden, a ki67 index <20% and will respond to PRRT irrespective to primary tumor. Nevertheless, we have mostly prognostic than predictive factors to predict the efficacy of PRRT in individual patients, while a promising tool could be the NETest. However, to date, the identikit of the perfect patient for PRRT is a puzzle without some pieces and still we cannot disregard a multidisciplinary discussion of the individual case to select the patients who will mostly benefit from PRRT.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Organometálicos / Tumores Neuroendócrinos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Organometálicos / Tumores Neuroendócrinos Idioma: En Ano de publicação: 2021 Tipo de documento: Article