2020
DOI: 10.1007/s00259-020-05127-9
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Therapy-related myeloid neoplasm after peptide receptor radionuclide therapy (PRRT) in 1631 patients from our 20 years of experiences: prognostic parameters and overall survival

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Cited by 22 publications
(25 citation statements)
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“…The most important long-term complications include myelodysplastic syndrome, acute myeloid leukemia, or bone marrow aplasia with the median latency period at diagnosis about 41 months ( 26 ). The prevalence of those severe, delayed adverse hematological events is estimated at 1.4%–4% ( 27 , 28 ). In case of PRRT radiopharmaceuticals labeled with 90Y, kidney-related toxicity should also be considered ( 29 ).…”
Section: Discussionmentioning
confidence: 99%
“…The most important long-term complications include myelodysplastic syndrome, acute myeloid leukemia, or bone marrow aplasia with the median latency period at diagnosis about 41 months ( 26 ). The prevalence of those severe, delayed adverse hematological events is estimated at 1.4%–4% ( 27 , 28 ). In case of PRRT radiopharmaceuticals labeled with 90Y, kidney-related toxicity should also be considered ( 29 ).…”
Section: Discussionmentioning
confidence: 99%
“…Patients with bone metastases present a higher risk of myelotoxicity [156]. Finally, acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) are severe long-term complications related to PRRT and were reported to occur in approximately 0.5 and 1.5% of patients, respectively, after a median of 55 and 28 months following PRRT [11,136,157]. Patients that have received prior alkylating chemotherapy are at greater risk of developing MDS/acute leukemia following PRRT [158,159] Radiolabeled SSTR2 antagonists, such as 177Lu-satoreotide tetraxetan, have shown higher tumor uptake, independent of SSTR activation, and greater tumor-to-organ ratios than agonists in preclinical models [160].…”
Section: Somatostatin Receptors and Other Unique Targets In Nets 41 Rationale For Targeting Sstmentioning
confidence: 99%
“…The origin of radiation-induced t-MN is very intricate and includes the formation of single or double strand breaks in the DNA, which can eventually lead to genetic mutations, including loss of function or oncogene activation [ 89 ]. Studies including large datasets, report an incidence of PHD after PRRT between 1.8 and 4.8%, with a median latency of 41 months [ 89 , 97 , 98 , 99 ]. Brieau et al reported an incidence of t-MN of 20% after PRRT, in a limited subgroup of 20 patients heavily pretreated with alkylating chemotherapy [ 100 ].…”
Section: Toxicitymentioning
confidence: 99%