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A Multi-Institutional Study of Magnetic Resonance/Ultrasound Fusion-Guided Nanoparticle-Directed Focal Therapy for Prostate Ablation.
Canfield, Steven E; George, Arvin K; Jue, Joshua S; Lewis, Sara C; Davenport, Matthew S; Tammisetti, Varaha S; Maruf, Mahir; Borregalaes, Leonardo D; Kadria-Vili, Yara; Schwartz, Jon A; West, Jennifer; Halas, Naomi J; Rastinehad, Ardeshir R.
Afiliação
  • Canfield SE; Division of Urology, Department of Surgery, UTHealth, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, Texas.
  • George AK; Department of Urology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
  • Jue JS; Smith Institute for Urology at Lenox Hill Hospital, Northwell Health, Zucker School of Medicine at Hofstra/Northwell, New York, New York.
  • Lewis SC; Department of Radiology, Mount Sinai, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Davenport MS; Department of Radiology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
  • Tammisetti VS; Department of Diagnostic and Interventional Imaging, UTHealth, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, Texas.
  • Maruf M; Smith Institute for Urology at Lenox Hill Hospital, Northwell Health, Zucker School of Medicine at Hofstra/Northwell, New York, New York.
  • Borregalaes LD; Department of Urology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
  • Kadria-Vili Y; Clinical Research, Nanospectra Biosciences, Inc., Houston, Texas.
  • Schwartz JA; Clinical Research, Nanospectra Biosciences, Inc., Houston, Texas.
  • West J; School of Engineering and Applied Science, University of Virginia, Charlottesville, Virginia.
  • Halas NJ; Smalley-Curl Institute and the Department of Electrical and Computer Engineering, Rice University, Houston, Texas.
  • Rastinehad AR; Smith Institute for Urology at Lenox Hill Hospital, Northwell Health, Zucker School of Medicine at Hofstra/Northwell, New York, New York.
J Urol ; : 101097JU0000000000004222, 2024 Sep 03.
Article em En | MEDLINE | ID: mdl-39226591
ABSTRACT

PURPOSE:

Focal therapy aims to provide a durable oncologic treatment option for men with prostate cancer (PCa), while preserving their quality of life. Most focal therapy modalities rely on the direct tissue effect, resulting in a possible nontargeted approach to ablation. Here, we report the results of the first human feasibility trial utilizing nanoparticle-directed focal photothermal ablation for PCa. MATERIALS AND

METHODS:

A prospective, open-label, single-arm, multicenter study of men with localized PCa in Gleason Grade Group 1 to 3 was conducted. Men received a single infusion of gold nanoparticles (AuroShells), followed by magnetic resonance (MR)/ultrasound (US) fusion-guided laser excitation of the target tissue to induce photothermal ablation. MRI was used to assess the effectiveness of prostate tissue ablation at 48 to 96 hours, 3 months, and 12 months post treatment. At 3 months, a targeted fusion biopsy of the lesion(s) was conducted. At 12 months, a targeted fusion biopsy and standard templated biopsy were performed. Treatment success was determined based on a negative MR/US fusion biopsy outcome within the treated area.

RESULTS:

Forty-six men were enrolled in the study, and 44 men with 45 lesions completed nanoparticle infusion and laser treatment. The mean PSA level at baseline was 9.5 ng/mL, which decreased to 5.9 ng/mL at 3 months and to 4.7 ng/mL at 12 months (P < .0001). The oncologic success rates at 3 and 12 months resulted in 29 (66%) and 32 (73%) of 44 patients, respectively, being successfully treated, confirmed with negative MR/US fusion biopsies within the ablation zone. Among Gleason Grade Group, maximum lesion diameter on MRI, prostate volume, and Prostate Imaging Reporting and Data System scoring, the maximum lesion diameter was significantly associated with the odds of treatment failure at 12 months (P = .046).

CONCLUSIONS:

Nanoparticle-directed focal laser ablation of neoplastic prostate tissue resulted in 73% of patients with successful treatment at 12 months post treatment, confirmed by negative MR/US fusion biopsy of the treated lesion and a systematic biopsy. CLINICAL TRIAL REGISTRATION NO. 02680535.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article