Real-World Experience with 177Lu-PSMA-617 Radioligand Therapy After Food and Drug Administration Approval

被引:8
作者
Tuchayi, Abuzar Moradi [1 ]
Yadav, Surekha [1 ]
Jiang, Fei [2 ]
Kim, Sarasa T. [1 ]
Saelee, Rachelle K. [1 ]
Morley, Amanda [1 ]
Juarez, Roxanna [1 ]
Lawhn-Heath, Courtney [1 ]
Wang, Yingbing [1 ]
de Kouchkovsky, Ivan [3 ]
Hope, Thomas A. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94117 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Med, Div Hematol & Oncol, San Francisco, CA USA
关键词
genitourinary; oncology; radionuclide therapy; 177; Lu-; PSMA-617; toxicities; RESISTANT PROSTATE-CANCER; CRITERIA; OUTCOMES; MEN;
D O I
10.2967/jnumed.123.266842
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We report our initial real -world experience with 177 Lu-PSMA-617 radioligand therapy. Methods: We performed a retrospective review of patients treated with 177 Lu-PSMA-617. Pretreatment PSMA PET, laboratory findings, overall survival, a fall in prostate -specific antigen by 50% (PSA50), and toxicities were evaluated. Results: Ninety-nine patients were included. Sixty patients achieved a PSA50. Seven of 18 (39%) patients who did not meet the TheraP PSMA imaging criteria achieved a PSA50. Nineteen of 31 (61%) patients who did not meet the VISION laboratory criteria achieved a PSA50. Sixty-three patients had a delay or stoppage in therapy, which was due to a good response in 19 patients and progressive disease in 14 patients. Of 10 patients with a good response who restarted treatment, 9 subsequently achieved a PSA50 on retreatment. The most common toxicities were anemia (33%) and thrombocytopenia (21%). Conclusion: At our center, patients who did not meet the TheraP PSMA imaging criteria or the VISION laboratory criteria benefited from 177 Lu-PSMA-617 radioligand therapy.
引用
收藏
页码:735 / 739
页数:5
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