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Third-line treatment and 177Lu-PSMA radioligand therapy of metastatic castration-resistant prostate cancer: a systematic review

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Publisher

SPRINGER
DOI: 10.1007/s00259-017-3895-x

Keywords

Prostate cancer; Lu-177-PSMA radioligand therapy; Abiraterone; Enzalutamide; Docetaxel; Cabazitaxel; Systematic review

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Aims There is a controversy as to the relative efficacy of Lu-177 prostate specific membrane antigen (PSMA) radioligand therapy (RLT) and third-line treatment for patients with metastatic castration-resistant prostate cancer (mCRPC). The aim of our systematic review was to elucidate whether Lu-177-PSMA RLT and third-line treatment have similar effects and adverse effects (PROSPERO ID CRD42017067743). Methods The review followed Preferred Reporting Items for Systematic Reviews and Meta-Analysis ( PRISMA) guidelines. Searches in Pubmed and Embase selected articles up to September 2017. A search in ClinicalTrials. gov indicated ongoing studies. The meta-analysis used the random-effects Results Twelve studies including 669 patients reported Lu-177-PSMA RLT. Overall, 43% of the patients had a maximum decline of PSA of >= 50% following treatment with Lu-177-PSMA RLT. The treatment with Lu-177-PSMA-617 and Lu-177-PSMA for imaging and therapy (I&T) had mainly transient adverse effects. Sixteen studies including 1338 patients reported third-line treatment. Overall, 21% of the patients had a best decline of PSA of >= 50% following third-line treatment. After third-line treatment with enzalutamide and cabazitaxel, adverse effects caused discontinuation of treatment for 10% to 23% of the patients. Lu-177-PSMA RLT gave a best PSA decline >= 50% more often than third-line treatment (mean 44% versus 22%, p = 0.0002, t test). Lu-177-PSMA RLT gave objective remission more often than third-line treatment (overall 31 of 109 patients versus 43 of 275 patients, p = 0.004, chi(2) test). Median survival was longer after Lu-177-PSMA RLT than after third-line treatment, but the difference was not statistically significant (mean 14 months versus 12 months, p = 0.32, t test). Adverse effects caused discontinuation of treatment more often for third-line treatment than for Lu-177-PSMA RLT (22 of 66 patients versus 0 of 469 patients, p < 0.001, chi(2) test). Conclusions As for patients with mCRPC, treatment with Lu-177-PSMA-617 RTL and Lu-177-PSMA I&T gave better effects and caused fewer adverse effects than third-line treatment.

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