Evidence map›Paper›PMID 39996439›Full record

ReviewInternational journal of urology : official journal of the Japanese Urological Association2025

Current Evidence on Cabazitaxel for Prostate Cancer Therapy: A Narrative Review.

Kazuhiro Suzuki, Hideyasu Matsuyama, Nobuaki Matsubara, Hirotaka Kazama, Fumiko Ueno, Hirotsugu Uemura

Abstract readReview
In one paragraph

Review in International journal of urology : official journal of the Japanese Urological Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kazuhiro SuzukiDepartment of Urology, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.ORCID https://orcid.org/0000-0002-1448-7273
Hideyasu MatsuyamaJA Yamaguchi Kouseiren Nagato General Hospital, Yamaguchi, Japan.
Nobuaki MatsubaraDepartment of Medical Oncology, National Cancer Center Hospital East, Chiba, Japan.ORCID https://orcid.org/0000-0002-9203-4245
Hirotaka KazamaSpecialty Care, Oncology Medical, Sanofi K.K., Tokyo, Japan.
Fumiko UenoSpecialty Care, Oncology Medical, Sanofi K.K., Tokyo, Japan.
Hirotsugu UemuraDepartment of Urology Kindai University Faculty of Medicine, Osakasayama, Japan.ORCID https://orcid.org/0000-0002-3665-9523

Funding

Sanofi
6 · The paper itself

Abstract

The incidence of prostate cancer (PC) has recently increased in Japan. Androgen deprivation therapy (ADT) has been a key treatment in patients with castration-sensitive PC (CSPC); however, resistance typically emerges through multiple mechanisms, leading to metastatic castration-resistant PC (mCRPC). Taxane-based therapy (i.e., docetaxel, cabazitaxel) has been standard care in patients with mCRPC. New evidence supporting the addition of androgen receptor signaling inhibitors (ARSIs, e.g., enzalutamide, abiraterone) to docetaxel and ADT for patients with metastatic CSPC (mCSPC) raises questions about the role of taxane-based therapies and their optimal sequencing, as well as how to identify patients who may benefit from taxane-based therapy. Here we review the evidence on taxane-based therapy, including cabazitaxel, in the treatment of PC, with a focus on clinical and real-world evidence from Japan. Cabazitaxel has proven effective for patients with mCRPC who have a history of ARSI and docetaxel use, and it is preferable to a second alternative ARSI, as indicated in the CARD study. The safety profile of cabazitaxel (particularly, the incidence of neutropenia) can be managed through prophylactic use of granulocyte colony-stimulating factor, as well as a lower dosage and possibly variation of the dosage interval. However, a certain dose intensity is required because neutropenia has been identified as a potential prognostic indicator for treatment effectiveness. In the ARSI era for mCSPC, evidence on mCRPC treatment sequencing is limited. A better understanding of PC biology and the collection of real-world data is essential for effective treatment and improved safety-benefit outcomes.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantTaxoidsAndrogen AntagonistsAndrogen Receptor AntagonistsDocetaxelDrug Resistance, NeoplasmHumansJapanMaleTreatment OutcomeAndrogen AntagonistsAndrogen Receptor AntagonistscabazitaxelDocetaxelTaxoidscabazitaxelchemotherapydocetaxelmetastatic castration‐resistant prostate cancermetastatic castration‐sensitive prostate cancer

Identifiers

PMID39996439
PMCPMC12022742

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.