Single Center Experience with a 4-Week 177Lu-PSMA-617 Treatment Interval in Patients with Metastatic Castration-Resistant Prostate Cancer
| dc.contributor.author | Kemppainen Jukka | |
| dc.contributor.author | Kangasmäki Aki | |
| dc.contributor.author | Malaspina Simona | |
| dc.contributor.author | Pape Bernd | |
| dc.contributor.author | Jalomäki Jarno | |
| dc.contributor.author | Kairemo Kalevi | |
| dc.contributor.author | Kononen Juha | |
| dc.contributor.author | Joensuu Timo | |
| dc.contributor.organization | fi=kliininen fysiologia ja isotooppilääketiede|en=Clinical Physiology and Isotope Medicine| | |
| dc.contributor.organization | fi=tyks, vsshp|en=tyks, varha| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.75985703497 | |
| dc.contributor.organization-code | 2607322 | |
| dc.converis.publication-id | 178068307 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/178068307 | |
| dc.date.accessioned | 2025-08-27T21:45:04Z | |
| dc.date.available | 2025-08-27T21:45:04Z | |
| dc.description.abstract | <p><strong>Background: </strong><sup>177</sup>Lu-PSMA-617 is a promising theragnostic treatment for metastatic castration-resistant prostate cancer (mCRPC). However, both the optimal treatment dose and interval in mCRPC and the rate of identification of responders from non-responders among possible treatment candidates are unknown.</p><p><strong>Methods: </strong>62 men with mCRPC who were treated with <sup>177</sup>Lu-PSMA-617 during 1/2017-2/2019 were included in the study. Treatment responses, overall survival (OS) and progression free survival (PFS) were determined. The median follow-up time was 1.4 years (IQR 0.5-2.2). Tumor volume of metastases (MTV), SUVmax and tumor lesion activity (TLA) were quantitated from pre-treatment PSMA PET/CT images together with pre-treatment PSA.</p><p><strong>Results: </strong>An average of three treatment cycles (2-5) were given within a four-week interval. PFS was 4.9 months (2.4-9.6) and OS was 17.2 months (6-26.4). There were no major adverse events reported. A significant PSA response of >50% was found in 58.7% of patients, which was significantly associated with longer OS, <em>p</em> < 0.004. PSA response was not associated with staging PSMA-derived parameters.</p><p><strong>Conclusions: </strong><sup>177</sup>Lu-PSMA-617 treatment in four-week intervals was safe and effective. Almost 60% of patients had a significant PSA response, which was associated with better OS. Pre-treatment PSA kinetics or staging PSMA PET/CT-derived parameters were not helpful in identifying treatment responders from non-responders; better biomarkers are needed to aid in patient selection.</p> | |
| dc.identifier.jour-issn | 2072-6694 | |
| dc.identifier.olddbid | 201032 | |
| dc.identifier.oldhandle | 10024/184059 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/47467 | |
| dc.identifier.urn | URN:NBN:fi-fe202301265891 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Kemppainen, Jukka | |
| dc.okm.affiliatedauthor | Malaspina, Simona | |
| dc.okm.affiliatedauthor | Dataimport, tyks, vsshp | |
| dc.okm.discipline | 3122 Cancers | en_GB |
| dc.okm.discipline | 3126 Surgery, anesthesiology, intensive care, radiology | en_GB |
| dc.okm.discipline | 3122 Syöpätaudit | fi_FI |
| dc.okm.discipline | 3126 Kirurgia, anestesiologia, tehohoito, radiologia | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher.country | Switzerland | en_GB |
| dc.publisher.country | Sveitsi | fi_FI |
| dc.publisher.country-code | CH | |
| dc.relation.articlenumber | 6155 | |
| dc.relation.doi | 10.3390/cancers14246155 | |
| dc.relation.ispartofjournal | Cancers | |
| dc.relation.issue | 24 | |
| dc.relation.volume | 14 | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/184059 | |
| dc.title | Single Center Experience with a 4-Week 177Lu-PSMA-617 Treatment Interval in Patients with Metastatic Castration-Resistant Prostate Cancer | |
| dc.year.issued | 2022 |
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