A plain language summary of the results from the MAGNITUDE study assessing how effective and how safe niraparib and abiraterone acetate with prednisone is in patients with metastatic castration-resistant prostate cancer Editorial


Authors: Chi, K. N.; Rathkopf, D.; Smith, M. R.; Efstathiou, E.; Attard, G.; Olmos, D.; Lee, J. Y.; Small, E. J.; Pereira de Santana Gomes, A. J.; Roubaud, G.; Saad, M.; Zurawski, B.; Sakalo, V.; Mason, G. E.; Francis, P.; Wang, G.; Wu, D.; Diorio, B.; Lopez-Gitlitz, A.; Sandhu, S.
Title: A plain language summary of the results from the MAGNITUDE study assessing how effective and how safe niraparib and abiraterone acetate with prednisone is in patients with metastatic castration-resistant prostate cancer
Abstract: Plain Language Summary: What is this summary about? This is a summary of the MAGNITUDE clinical study that was published in the Journal of Clinical Oncology (March 2023) and in Annals of Oncology (September 2023). Researchers looked at the combination of niraparib and abiraterone acetate with prednisone as a first treatment for adult patients with metastatic castration-resistant prostate cancer. Researchers wanted to know how effective and safe niraparib + abiraterone acetate with prednisone is in patients whose cancers had certain gene changes. Researchers focused on genes related to homologous recombination repair (HRR), a normal process that repairs damaged DNA. The best understood HRR genes are BRCA1 and BRCA2 (which code for BReast CAncer susceptibility 1 and 2 proteins) that are changed in 3–13% of patients with metastatic castration-resistant prostate cancer. We refer to these genes as BRCA1/2. Compared with cancers that lack these changes, cancers with changes in HRR genes (HRR+) may not respond as well to treatments that are normally used for metastatic castration-resistant prostate cancer, such as abiraterone acetate with prednisone. What were the main conclusions reported by the researchers? Patients who had BRCA1/2 changes had a longer time (16.6 months) before their cancer worsened compared with those who did not (10.9 months). Patients with HRR+ metastatic castration-resistant prostate cancer taking niraparib + abiraterone acetate with prednisone had a longer time (16.5 months) before their cancer worsened (tumor increased in size, cancer spread, or death) compared with those taking placebo + abiraterone acetate with prednisone (13.7 months). Patients taking niraparib + abiraterone acetate with prednisone had more side effects (99.1%) than those taking placebo + abiraterone acetate with prednisone (94.3%). These were well-known side effects of these medicines and generally managed by pausing treatment or lowering the dose. What are the key takeaways? Patients with HRR+ metastatic castration-resistant prostate cancer, especially those with BRCA1/2 changes, have better outcomes with niraparib + abiraterone acetate with prednisone compared with placebo + abiraterone acetate with prednisone. These results show the importance of testing for HRR gene changes to select treatments that are most likely to lead to improved outcomes for these patients. This is an abstract of the Plain Language Summary of Publication article. View the full Plain Language Summary PDF of this article to read the full-text. © 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
Keywords: adult; clinical article; treatment outcome; prednisone; mortality; neutropenia; placebo; chemotherapy; nuclear magnetic resonance imaging; antineoplastic agent; dna repair; metastasis; progression free survival; computer assisted tomography; anemia; thrombocytopenia; antineoplastic combined chemotherapy protocols; randomized controlled trials as topic; pathology; prostate cancer; hospitalization; cancer cell; spinal cord compression; neoplasm metastasis; piperidines; abiraterone acetate; drug therapy; androgen deprivation therapy; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; testosterone; medicine; reproduction; castration resistant prostate cancer; randomized controlled trial (topic); indazoles; piperidine derivative; niraparib; recombination repair; humans; human; male; article; prostatic neoplasms, castration-resistant; metastatic castration resistant prostate cancer; plain language summary; indazole derivative; plain language summaries
Journal Title: Future Oncology
Volume: 21
Issue: 9
ISSN: 1479-6694
Publisher: Future Medicine  
Date Published: 2025-01-01
Start Page: 1013
End Page: 1031
Language: English
DOI: 10.1080/14796694.2025.2470106
PUBMED: 40159790
PROVIDER: scopus
PMCID: PMC11988215
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Dana Elizabeth Rathkopf
    273 Rathkopf