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Epidemiology, treatment patterns, and clinical outcomes in de novo oligometastatic hormone-sensitive prostate cancer.
Gong, Jun; Janes, Jessica L; Trustram Eve, Claire; Stock, Shannon; Waller, Justin; De Hoedt, Amanda M; Kim, Jeri; Ghate, Sameer R; Shui, Irene M; Freedland, Stephen J.
Afiliación
  • Gong J; Division of Urology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Janes JL; Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Trustram Eve C; Department of Surgery, Durham Veterans Affairs Health Care System, Durham, North Carolina, USA.
  • Stock S; Department of Surgery, Durham Veterans Affairs Health Care System, Durham, North Carolina, USA.
  • Waller J; Department of Surgery, Durham Veterans Affairs Health Care System, Durham, North Carolina, USA.
  • De Hoedt AM; Department of Mathematics and Computer Science, College of the Holy Cross, Worcester, Massachusetts, USA.
  • Kim J; Department of Surgery, Durham Veterans Affairs Health Care System, Durham, North Carolina, USA.
  • Ghate SR; Department of Surgery, Durham Veterans Affairs Health Care System, Durham, North Carolina, USA.
  • Shui IM; Merck & Co., Inc, Rahway, New Jersey, USA.
  • Freedland SJ; Merck & Co., Inc, Rahway, New Jersey, USA.
Cancer ; 2024 Jul 01.
Article en En | MEDLINE | ID: mdl-38950063
ABSTRACT

BACKGROUND:

This study was conducted to better characterize the epidemiology, clinical outcomes, and current treatment patterns of de novo oligometastatic hormone-sensitive prostate cancer (omHSPC) in the United States Veterans Affairs Health Care System.

METHODS:

In this observational retrospective cohort study, 400 de novo metastatic hormone-sensitive PC (mHSPC) patients diagnosed from January 2015 to December 2020 (follow-up through December 2021) were randomly selected. omHSPC was defined as five or less total metastases (excluding liver) by conventional imaging. Kaplan-Meier methods estimated overall survival (OS) and castration-resistant prostate cancer (CRPC)-free survival from mHSPC diagnosis date and a log-rank test compared these outcomes by oligometastatic status.

RESULTS:

Twenty percent (79 of 400) of de novo mHSPC patients were oligometastatic. Most baseline characteristics were similar by oligometastatic status; however, men with non-omHSPC had higher median prostate-specific antigen at diagnosis (151.7) than omHSPC (44.1). First-line (1L) novel hormonal therapy was similar between groups (20%); 1L chemotherapy was lower in omHSPC (5%) versus non-omHSPC (14%). More omHSPC patients received metastasis-directed therapy/prostate radiation therapy (14%) versus non-omHSPC (2%). Median OS and CRPC-free survival (in months) were higher in omHSPC versus non-omHSPC (44.4; 95% confidence interval [CI], 33.9-not estimated vs. 26.2; 95% CI, 20.5-32.5, p = .0089 and 27.6; 95% CI, 22.1-37.2 vs. 15.3; 95% CI, 12.8-17.9, p = .0049), respectively.

CONCLUSIONS:

Approximately 20% of de novo mHSPC were oligometastatic, and OS was significantly longer in omHSPC versus non-omHSPC. Although potentially "curative" therapy use was higher in omHSPC versus non-omHSPC, the percentages were still relatively low. Future studies are warranted given potential for prolonged responses with multimodal therapy inclusive of systemic and local therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos