Afshar-Oromieh Ali, Haberkorn Uwe, Zechmann Christian, Armor Thomas, Mier Walter, Spohn Fabian, Debus Nils, Holland-Letz Tim, Babich John, Kratochwil Clemens
Department of Nuclear Medicine, Heidelberg University Hospital, INF 400, 69120, Heidelberg, Germany.
Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg, Germany.
Eur J Nucl Med Mol Imaging. 2017 Jun;44(6):950-959. doi: 10.1007/s00259-017-3665-9. Epub 2017 Mar 9.
Prostate-specific membrane antigen (PSMA)-targeting radioligand therapy (RLT) was introduced in 2011. The first report described the antitumor and side effects of a single dose. The aim of this analysis was to evaluate toxicity and antitumor activity after single and repetitive therapies.
Thirty-four men with metastatic castration-resistant prostate cancer received PSMA-RLT with I-MIP-1095. Twenty-three patients received a second, and three patients a third dose, timed at PSA progression after an initial response to the preceding therapy. The applied doses were separated in three groups: <3.5, 3.5-5.0 and >5.0 GBq. Antitumor and side-effects were analyzed by blood samples and other clinical data. Follow-up was conducted for up to 5 years.
The best therapeutic effect was achieved by the first therapy. A PSA decline of ≥50% was achieved in 70.6% of the patients. The second and third therapies were significantly less effective. There was neither an association between the applied activity and PSA response or the time-to-progression. Hematologic toxicities were less prevalent but presented in a higher percentage of patients with increasing number of therapies. After hematologic toxicities, xerostomia was the second most frequent side effect and presented more often and with higher intensity after the second or third therapy.
The first dose of RLT with I-MIP-1095 presented with low side effects and could significantly reduce the tumor burden in a majority of patients. The second and third therapies were less effective and presented with more frequent and more intense side effects, especially hematologic toxicities and xerostomia.
前列腺特异性膜抗原(PSMA)靶向放射性配体疗法(RLT)于2011年被引入。首篇报告描述了单次给药的抗肿瘤作用及副作用。本分析的目的是评估单次及重复治疗后的毒性和抗肿瘤活性。
34例转移性去势抵抗性前列腺癌男性患者接受了I-MIP-1095的PSMA-RLT治疗。23例患者接受了第二次给药,3例患者接受了第三次给药,给药时间为在前次治疗出现初始反应后PSA进展时。所应用的剂量分为三组:<3.5、3.5 - 5.0和>5.0 GBq。通过血液样本及其他临床数据分析抗肿瘤作用及副作用。随访时间长达5年。
首次治疗取得了最佳治疗效果。70.6%的患者PSA下降≥50%。第二次和第三次治疗的效果明显较差。所应用的活度与PSA反应或疾病进展时间之间均无关联。血液学毒性的发生率较低,但随着治疗次数增加,出现血液学毒性的患者比例更高。血液学毒性之后,口干是第二常见的副作用,在第二次或第三次治疗后出现得更频繁且强度更高。
I-MIP-1095的首次RLT给药副作用低,且能在大多数患者中显著减轻肿瘤负担。第二次和第三次治疗效果较差,且副作用更频繁、强度更高,尤其是血液学毒性和口干。