Phase II trial of image-guided oligometastatectomy and radiation therapy in recurrent prostate cancer (SOAR).

A Alejandro Sanchez (University of Utah, Salt Lake City, UT) U Umang Swami (Division of Medical Oncology Department of Internal Medicine Huntsman Cancer Institute University of Utah Salt Lake City Utah USA) B Bogdana Schmidt (Huntsman Cancer Institute, University of Utah, Salt Lake City, UT) C Christopher B. Dechet (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) K Kenneth M Boucher (Huntsman Cancer Institute, University of Utah, Salt Lake City, UT) L Lisa Chapman (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) H Hillary Davis (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) J Jeff Linton (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) E Erica Farr (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) S Samuel Leonhart (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) J Josiah Hawks (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) S Skyler B Johnson (Hunstman Cancer Institute at the University of Utah, Salt Lake City, UT) J Jonathan David Tward (University of Utah, Salt Lake City, UT) B Bismarck Odei (Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT) S Sumati Gupta (Huntsman Cancer Institute at The University of Utah, Salt Lake City, UT) N Neeraj Agarwal (Division of Medical Oncology Department of Internal Medicine Huntsman Cancer Institute University of Utah Salt Lake City Utah USA) B Brock ONeil (Hunstman Cancer Institute at the University of Utah, Salt Lake City, UT) B Benjamin L. Maughan (University of Utah, Salt Lake City, UT)

Abstract

38 Background: In a subset of patients with molecular-imaging defined recurrent oligometastatic prostate cancer (PCa), salvage oligometastatectomy with surgery and/or radiation may provide improved androgen deprivation therapy (ADT)-free survival. Methods: This is a phase II trial with oligorecurrent PCa after primary prostatectomy or radiation therapy detected on Axumin (n=11) or Prostate-Specific Membrane Antigen (PSMA) (n=9) positron emission tomography. Oligometastatic disease was defined as ≤ 10 total sites, either of lymph node (LN) only (Group A), bone only (Group B), or LN and bone (Group C). Surgical intervention for patients with LN disease included extended pelvic and/or retroperitoneal LN dissection, depending on the location of the LNs. Groups A and C received adjuvant IMRT without ADT if PSA response was ≥ 1/3 decrease but remained ≥ 0.2 ng/dL. The primary outcome was a reduction in PSA by ≥ 50% at 6 months. Secondary objectives included PSA progression free-survival (PSA-PFS), ADT-free survival, and safety. Results: We accrued a total of 20 patients. The median age was 65 years (IQR 61-70), 95% (19/20) had an ECOG of 0, and 10% (2/20) were Hispanic. All patients had a prior prostatectomy, after which 45% (9/20) received adjuvant/salvage RT, with 33% (3/9) including the pelvis/ prostate bed. 30% (6/20) had exposure to ADT before trial treatment. The median time from definitive prostate cancer treatment to trial treatment was 2.8 years (IQR: 0.9-6.0). Oligorecurrent disease occurred as lymph nodes only (18/20; 90%) or bony (2/20; 10%). Within Group A, one patient completed adjuvant RT. The average number of imaging-identified positive LNs was 1.8 (range 1-6). The primary endpoint of reduction in PSA by ≥ 50% at 6 months was 40% (95%CI 19-64%) (Table 1). The secondary endpoint of PSA-PFS at 12 months was 84.4% (95%CI 66.6-100%). ADT-free survival at 12-months was 71.4% (95% CI 52.7% - 96.6%). There were no Clavien Grade III-IV complications. Conclusions: Salvage treatment of oligometastatic disease after prostatectomy or radiation identified on molecular imaging is feasible and safe. Nearly half the cohort had a good response to salvage treatment, demonstrated by a ≥ 50% reduction in PSA at 6 months. Ongoing analyses include comparing imaging and pathology correlations, and comparing complete/ partial responders and treatment failure. Further research is needed to identify ideal candidates for salvage treatment. Clinical trial information: NCT03796767 . PSA progression-free survival at 6- and 12-months (PFS). Time Estimate 95% Confidence Interval 6 months 100% --- 12 months 84.4% 66.6-100%

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 38-38
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

A

Alejandro Sanchez

University of Utah, Salt Lake City, UT

U

Umang Swami

Division of Medical Oncology Department of Internal Medicine Huntsman Cancer Institute University of Utah Salt Lake City Utah USA

B

Bogdana Schmidt

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

C

Christopher B. Dechet

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

K

Kenneth M Boucher

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

L

Lisa Chapman

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

H

Hillary Davis

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

J

Jeff Linton

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

E

Erica Farr

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

S

Samuel Leonhart

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

J

Josiah Hawks

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

S

Skyler B Johnson

Hunstman Cancer Institute at the University of Utah, Salt Lake City, UT

J

Jonathan David Tward

University of Utah, Salt Lake City, UT

B

Bismarck Odei

Huntsman Cancer Institute at the University of Utah, Salt Lake City, UT

S

Sumati Gupta

Huntsman Cancer Institute at The University of Utah, Salt Lake City, UT

N

Neeraj Agarwal

Division of Medical Oncology Department of Internal Medicine Huntsman Cancer Institute University of Utah Salt Lake City Utah USA

B

Brock ONeil

Hunstman Cancer Institute at the University of Utah, Salt Lake City, UT

B

Benjamin L. Maughan

University of Utah, Salt Lake City, UT