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Buzogány, István

Mayo Clinic

Péterfy Sándor Utcai Kórház-Rendelőintézet és Baleseti Központ

Citations 2

A phase 2 study of 99m Tc-trofolastat chloride (MIP-1404) SPECT/CT to identify and localize prostate cancer (PCa) in high-risk patients (pts) undergoing radical prostatectomy (RP) and extended pelvic lymph node (ePLN) dissection compared to hist
Slawin, Kevin M., Tenke, Péter , Joniau, Steven , Ellis, William J., Buzogány, István, Мишугин, С. В. , Stolz, Josef, Матвеев, В. Б. , Karnes, R. Jeffrey , Jarrard, David Frasier, Yuh, Bertram, Trabulsi, Edouard J. , Stambler, Nancy , Armor, Thomas, Israel, Robert J. , Joniau, Steven , Alekseev, B. Yа. , Klein, Eric A. , Študent, Vladimír , Scherr, Douglas S. , Babich, John W.

Journal of Clinical Oncology | January 3, 2019 | Volume: 32 | Issue: 15_suppl | Pages: e16003-e16003

10.1200/jco.2014.32.15_suppl.e16003 Get It

A phase II study of 99mTc-trofolastat (MIP-1404) SPECT/CT to identify and localize prostate cancer in high-risk patients undergoing radical prostatectomy (RP) and extended pelvic lymph node dissection (EPLND) compared to histopathology: An inter
Slawin, Kevin M., Ellis, William J., Tenke, Péter , Joniau, Steven , Buzogány, István, Мишугин, С. В. , Karnes, R. Jeffrey , Yuh, Bertram, Jarrard, David Frasier, Trabulsi, Edouard J. , Stolz, Josef, Youssoufian, Hagop , Stambler, Nancy , Armor, Thomas, Israel, Robert J. , Alekseev, B. Yа. , Klein, Eric A. , Scherr, Douglas S. , Babich, John W. , Joniau, Steven

Journal of Clinical Oncology | February 24, 2017 | Volume: 32 | Issue: 4_suppl | Pages: 94-94

10.1200/jco.2014.32.4_suppl.94 Get It

94 Background: Technetium (Tc99m) trofolastat (USANC) is a novel urea-based small molecule SPECT radiotracer with utility in imaging overexpression of PSMA in prostate cancer (PCa). Unlike earlier agents targeting PSMA, this ligand is rapidly internalized and retained in tumors. We conducted an open-label, multicenter phase 2 study in the US and Europe (NCT01667536). An interim analysis was performed at approximately 50% accrual. Methods: Patients (pts) with confirmed adenocarcinoma of the prostate scheduled for RP with EPLND at high risk for disease outside of the prostate gland were eligible. High risk pts were ≥cT3 or Kattan nomogram score ≥130. Within 30 days of screening, pts required a bone scan and pelvic MRI. After enrollment, pts received trofolastat followed by whole-body planar and SPECT/CT imaging 3 to 6 hrs later. Pts then underwent RP with EPLND within 21 days. SPECT/CT images were evaluated centrally by 3 readers blinded to clinical information and compared to on-site pathology assessments using a common scoring template. The primary endpoint was the ability of trofolastat to detect PCa within the gland. Secondary endpoints included detection of extent and location within the gland, pelvic lymph nodes and comparative performance against MRI. Results: 84 pts were enrolled to date from 16 centers. Interim data is available for 54 pts. A majority (≥2/3) of SPECT/CT readers correctly identified the presence or absence of primary PCa in 51/54 (94%, 85-98 95% CI) patients including 2 true-negative cases treated with neoadjuvant enzalutamide. Sensitivity and specificity were 94% (84-98 95% CI) and 100% (34-100 95% CI) respectively. Conclusions: Based on the interim data available, trofolastat has accurately detected primary prostate carcinoma within the gland with high sensitivity and specificity in high-risk pts prior to surgery. Updated results, analyses of secondary endpoints, pelvic lymph nodes, and comparative performance vs. MRI from this ongoing study will be presented. Clinical trial information: NCT01667536. [Table: see text]