Docetaxel versus abiraterone for metastatic hormone-sensitive prostate cancer with focus on efficacy of sequential therapy.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
05 2023
Historique:
revised: 11 12 2022
received: 13 10 2022
accepted: 30 12 2022
pubmed: 21 1 2023
medline: 25 3 2023
entrez: 20 1 2023
Statut: ppublish

Résumé

We aimed to assess the oncologic efficacy of combining docetaxel (DOC) versus abiraterone (ABI) with androgen deprivation therapy (ADT) in patients with high-risk metastatic hormone-sensitive prostate cancer (mHSPC), with a focus on the efficacy of sequential therapy, in a real-world clinical practice setting. The records of 336 patients who harbored de novo high-risk mHSPC, based on the LATITUDE criteria, and had received ADT with either DOC (n = 109) or ABI (n = 227) were retrospectively analyzed. Overall survival (OS), cancer-specific survival (CSS), progression-free survival (PFS), including time to castration-resistant prostate cancer (CRPC), time to 2nd-line progression (PFS2), and 2nd- and 3rd-line PFS, were compared. We used one-to-two propensity score matching to minimize the confounders. The differential efficacy of 2nd-line therapy based on agents in each arm was evaluated using the unmatched cohort as an additional interest. After propensity score matching, 86 patients treated with DOC + ADT and 172 with ABI + ADT were available for analyses. The 3-year OS and CSS for DOC versus ABI were 76.2% versus 75.1% (p = 0.8) and 78.2% versus 78.6% (p = 1), respectively. There was no difference in the median PFS2 (49 vs. 43 months, p = 0.39), while the median time to CRPC in patients treated with ABI was significantly longer compared to those treated with DOC (42 vs. 22 months; p = 0.006). The median 2nd-line PFS (14 vs. 4 months, p < 0.001) and 3rd-line PFS (4 vs. 2 months, p = 0.012) were significantly better in the DOC group than in the ABI group. Among the unmatched cohort, after ABI for mHSPC, the median 2nd-line PFS did not differ between the patients treated with DOC and those treated with enzalutamide as 2nd-line therapy (both 3 months, p = 0.8). ADT with DOC or ABI has comparable oncologic outcomes in terms of OS, CSS, and PFS2 in patients with de novo high-risk mHSPC. Compared to DOC, ABI resulted in longer time to CRPC but worse 2nd and 3rd-line PFS. Further studies are needed to clarify the optimal sequence of therapy in the upfront intensive treatment era.

Identifiants

pubmed: 36661102
doi: 10.1002/pros.24488
doi:

Substances chimiques

Docetaxel 15H5577CQD
abiraterone G819A456D0
Androgen Antagonists 0
Hormones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

563-571

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

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Auteurs

Takafumi Yanagisawa (T)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Kenichi Hata (K)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Department of Urology, Atsugi City Hospital, Kanagawa, Japan.

Shintaro Narita (S)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Shingo Hatakeyama (S)

Department of Urology, Division of Advanced Blood Purification Therapy, Hirosaki University Graduate School of Medicine, Aomori, Japan.

Keiichiro Mori (K)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Yuji Yata (Y)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Takayuki Sano (T)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Takashi Otsuka (T)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Shuhei Hara (S)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Keiichiro Miyajima (K)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Yuki Enei (Y)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Wataru Fukuokaya (W)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Minoru Nakazono (M)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Akihiro Matsukawa (A)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Jun Miki (J)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Tomonori Habuchi (T)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Chikara Ohyama (C)

Department of Urology, Division of Advanced Blood Purification Therapy, Hirosaki University Graduate School of Medicine, Aomori, Japan.

Shahrokh F Shariat (SF)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia.
Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, Jordan.
Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Department of Urology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.
Department of Urology, Weill Cornell Medical College, New York, New York, USA.
Karl Landsteiner Institute of Urology and Andrology, Vienna, Austria.

Takahiro Kimura (T)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

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