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Benjamin P. Saylor is associate editor of Urology Times, an Advanstar Communications publication.

The Cancer BioShield platform is being assessed as a treatment for lymphopenia in adult patients with refractory or relapsed solid tumors, including genitourinary tumors.

FDA authorizes Expanded Access Program of Anktiva for lymphopenia

professor and chair of urology at the University of Oklahoma Health Sciences Center in Oklahoma City, is co-editor in chief of 

"As clinicians, researchers, and advocates, this moment invites us to reflect on how far we’ve come—and how much further we must go," writes Michael S. Cookson, MD, MMHC, FACS.

Prostate cancer awareness in 2025: A human imperative in the wake of President Biden’s diagnosis

Data from the #HOPE4KIDNEY trial is intended to support submission for regulatory clearance of the Edison Histotripsy System.

Pivotal trial of histotripsy system for kidney tumors reaches enrollment goal

Data showed that Non-Hispanic Black and Latinx/Hispanic patients were less likely to receive PSMA-PET imaging than non-Hispanic White patients. 

Study finds racial/ethnic disparities in use of PSMA-PET in prostate cancer

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In this article, we describe our thought processes in treating patients with Peyronie's disease, which are summarized in an algorithm.

Streamlined management of Peyronie’s disease

Dr. De La Cerda provides an overview of a patient case involving a 68 year-old male presenting with severe back pain, with an analysis of the clinical presentation, workup, and medical history.

Bone Predominant mCRPC Patient Case

Video content above is prompted by the following:

What are your initial impressions of the case?

Video Series

The FDA has accepted a Biologics License Application (BLA) seeking approval of nivolumab (Opdivo) co-formulated with Halozyme’s proprietary recombinant human hyaluronidase (rHuPH20), or subcutaneous nivolumab, for the treatment of patients with all previously approved solid tumor indications for nivolumab as a monotherapy, monotherapy maintenance following completion of combination therapy with nivolumab plus ipilimumab (Yervoy), or in combination with chemotherapy or cabozantinib (Cabometyx).

Nivolumab is currently approved under several indications, including in combination with ipilimumab for the first-line treatment of patients with intermediate- or poor-risk advanced renal cell carcinoma (RCC), in combination with cabozantinib for the first-line treatment of patients with advanced RCC, for the treatment of patients with advanced RCC who have received prior anti-angiogenic therapy, and in combination with cisplatin and gemcitabine for the first-line treatment of patients with unresectable or metastatic urothelial carcinoma.

The FDA is set to have a decision regarding the subcutaneous nivolumab formulation on or by December 29, 2024.

 According to a news release from Bristol Myers Squibb,

 approval of the formulation would make it the first and only subcutaneously administered PD-1 inhibitor.

“We believe subcutaneous nivolumab has the potential to make a significant difference in the lives of patients, which is reinforced by the FDA’s acceptance of our application,” said Gina Fusaro, PhD, vice president, global program lead, Bristol Myers Squibb, in the news release.

 “Opdivo is a foundational PD-1 inhibitor approved for many different types of cancer, and our continued investment in research that puts patients first remains a priority. If approved by the FDA, the subcutaneous administration of nivolumab would provide patients and their physicians with a new option that delivers the same well-known benefits as IV Opdivo but with the improved convenience of an injection administered in 3 to 5 minutes rather than a 30-to-60-minute infusion.”

The BLA submission is supported by findings from the phase 3 CheckMate-67T trial (NCT04810078), in which subcutaneous nivolumab met the study’s co-primary end points by demonstrating noninferiority to intravenous (IV) nivolumab regarding time average nivolumab serum concentration over 28 days (C

; geometric mean ratio [GMR}, 2.098; 90% CI, 2.001-2.200) and minimum serum concentration at a steady state (C

Data from the study, which were presented at the 2024 American Society of Clinical Oncology Genitourinary Cancers Symposium in San Francisco, California,

 also showed that subcutaneous nivolumab demonstrated noninferiority to IV nivolumab in the key powered secondary end point of objective response rate (ORR). Specifically, the subcutaneous arm demonstrated an ORR of 24.2% (95% CI, 19.0-30.0) per blinded independent central review (BICR), compared with 18.2% (95% CI, 13.6-23.6) in the IV arm.

The safety profile for subcutaneous nivolumab was consistent with that of the IV formulation. Among patients who received the subcutaneous formulation, 8.1% experienced injection-site reactions, with all being low-grade and transient. Deaths due to study drug toxicity occurred in 3 patients in the subcutaneous arm and 1 patient in the IV arm. Most deaths that occurred during the study were due to disease progression.

In total, the phase 3, open-label CheckMate-67T trial enrolled 495 patients with advanced or metastatic ccRCC who had received prior systemic therapy. Patients were randomly assigned 1:1 to receive 1200 mg subcutaneous nivolumab plus rHuPH20 every 4 weeks (n = 248) or to 3 mg/kg IV nivolumab every 2 weeks (n = 247) for up to 2 years of treatment or until disease progression, unacceptable toxicity, withdrawal, or death.

The co-primary pharmacokinetic end points for noninferiority testing were C

 of subcutaneous nivolumab vs IV nivolumab. The key secondary end point was ORR per BICR.

Final completion of the CheckMate-67T study is expected in January 2026.

1. U.S. Food and Drug Administration accepts Bristol Myers Squibb’s application for subcutaneous nivolumab (nivolumab and hyaluronidase). News release. Bristol Myers Squibb. May 6, 2024. Accessed May 7, 2024. https://news.bms.com/news/corporate-financial/2024/U.S.-Food-and-Drug-Administration-Accepts-Bristol-Myers-Squibbs-Application-for-Subcutaneous-Nivolumab-nivolumab-and-hyaluronidase/default.aspx

2. Bristol Myers Squibb announces updated action date by the U.S. Food and Drug Administration for subcutaneous nivolumab (nivolumab and hyaluronidase). News release. Published online and accessed May 21, 2024. https://investors.bms.com/iframes/press-releases/press-release-details/2024/Bristol-Myers-Squibb-Announces-Updated-Action-Date-by-the-U.S.-Food-and-Drug-Administration-for-Subcutaneous-Nivolumab-nivolumab-and-hyaluronidase/default.aspx

3. George S, Bourlon TB, Chacon MR, et al. Subcutaneous nivolumab (NIVO SC) vs intravenous nivolumab (NIVO IV) in patients with previously treated advanced or metastatic clear cell renal cell carcinoma (ccRCC): Pharmacokinetics (PK), efficacy, and safety results from CheckMate 67T. 

4. A study of subcutaneous nivolumab versus intravenous nivolumab in participants with previously treated clear cell renal cell carcinoma that is advanced or has spread (CheckMate-67T). ClinicalTrials.gov. Last updated March 1, 2024. Accessed May 7, 2024. https://clinicaltrials.gov/study/NCT04810078

The FDA is set to have a decision regarding the subcutaneous nivolumab formulation on or by December 29, 2024. 

News

FDA accepts BLA for subcutaneous nivolumab in solid tumors

The FDA has authorized an Expanded Access Program (NCT06956547) for use of nogapendekin alfa inbakicept-pmln (NAI; Anktiva) to manage lymphopenia in adult patients with refractory or relapsed solid tumors, including genitourinary tumors, who have progressed after first-line standard-of-care treatment with chemotherapy, radiation, and/or checkpoint inhibitors, ImmunityBio announced in a news release.

The Expanded Access Program is specifically assessing the use of ImmunityBio’s Cancer BioShield platform, which includes NAI at its core. NAI was approved by the FDA in 2024 for the treatment of patients with BCG-unresponsive non–muscle invasive 

 (NMIBC) with carcinoma in situ (CIS) with or without papillary disease.

As part of the Cancer BioShield program, NAI “proliferates natural killer (NK) cells and CD4+ and CD8+ T cells, restoring lymphocyte levels critical for immunosurveillance, immunogenic cell death, and long-term tumor control,” ImmunityBio explained.

According to the company, the platform includes the following:

“In-vivo stimulation: Subcutaneous administration of ANKTIVA expands NK and T cells, boosting anti-tumor immunity.

Ex-vivo targeted cytotoxicity: Off-the-shelf PD-L1 t-haNK CAR-NK cells are engineered to target and eliminate PD-L1–expressing tumor cells and immunosuppressive neutrophils (myeloid-derived suppressor cells), enhancing anti-tumor specificity and reducing immune evasion.

Memory Cytokine-Enriched Natural Killer (M-ceNK) cell therapy: M-ceNK cells are developed via cytokine activation and expansion of autologous and allogeneic NK cells collected through apheresis, potentially providing long-term immune memory and sustained cytotoxic capacity.”

The BioShield platform was granted a Regenerative Medicine Advanced Therapy designation by the FDA in February 2025 for the management of lymphopenia.

For decades, epoetin alfa (epogen) and filgrastim (neupogen) have been used to treat patients with chemotherapy- and radiation-induced anemia and neutropenia, respectively. However, there has been no comparable option available for the management of lymphopenia.

®, Soon-Shiong explained, “To this day, there's never been a molecule, a fusion protein, that rescues lymphocytes, the NK cells and T cells, which are the key cells for killing cancer and generating memory. For the first time, this is Anktiva.”

Data from the phase 2 QUILT-88 study (NCT04390399) were recently presented at the 

2025 American Society of Clinical Oncology Annual Meeting

 Overall, the trial was assessing the use of NAI and PD-L1-targeted high-affinity NK cell therapy (PD-L1 t-haNK) in combination with low-dose chemotherapy in patients with locally advanced or metastatic pancreatic cancer.

Data showed that the chemo-immunotherapy protocol led to a median overall survival (OS) of 6.2 months (95% CI, 5.0 to 7.1) in the 3

 line setting and 5.7 months (95% CI, 4.3 to 6.4) in the 3

 line setting. According to the authors, a median OS exceeding 6 months is roughly 2 months greater than the OS achieved by other therapies in the 3

Additionally, a higher absolute lymphocyte count (ALC) was associated with greater survival. Median OS was 7.1 months in patients with an ALC of 1.045 x 109 cells/L or higher and a CA19-9 less than 4079.6 U/mL compared with a median OS of 3.1 months for patients with an ALC less than 1.045 x 109 cells/L and a CA19-9 of 4079.6 U/mL or higher (HR, 3.6; 

Grade 3 or higher treatment-emergent adverse events occurred in 95% of patients. These were largely attributed to chemotherapy, according to the authors.

“Lymphopenia has long been recognized as a major driver and predictor of early mortality in cancer—yet until now, it has remained unaddressed,” said Patrick Soon-Shiong, MD, founder, executive chairman, and global chief scientific and medical officer of ImmunityBio, in the news release.

 “This FDA authorization allows all patients with solid tumors suffering from immune collapse following first-line therapy of chemo, radiation, or immunotherapy to access ANKTIVA. The survival benefit we observed at ASCO 2025 in 3rd to 6th line advanced metastatic pancreatic cancer confirms that restoring lymphocyte levels—rather than depleting them—can change the course of disease.”

1. ImmunityBio receives FDA Expanded Access authorization for landmark treatment of lymphopenia with ANKTIVA, the Cancer BioShield Platform, in patients with solid tumors. News release. ImmunityBio. June 2, 2025. Accessed June 7, 2025. https://immunitybio.com/immunitybio-receives-fda-expanded-access-authorization-for-landmark-treatment-of-lymphopenia-with-anktiva-the-cancer-bioshield-platform-in-patients-with-solid-tumors/

2. Seery T, Nangia C, McKean H, et al. Association of lymphopenia rescue and CA19-9 levels with overall survival following IL-15 superagonist N-803 and PD-L1 t-haNK chemo-immunotherapy for 3rd line or greater metastatic pancreatic cancer. 2025. doi:10.1200/JCO.2025.43.16_suppl.2542. Abstract 2542

The FDA has authorized an Expanded Access Program for nogapendekin alfa inbakicept-pmln (NAI; Anktiva) to manage lymphopenia in patients with refractory or relapsed solid tumors. This program utilizes ImmunityBio’s Cancer BioShield platform, which enhances NK and T cell proliferation, crucial for immunosurveillance and tumor control. Data from the QUILT-88 study showed improved median overall survival in advanced pancreatic cancer patients using NAI and PD-L1-targeted NK cell therapy. The program addresses the unmet need for lymphopenia management, offering potential survival benefits in solid tumor patients.

The combination of zanzalintinib and nivolumab (Opdivo) showed promising efficacy and manageable safety in previously untreated stage 4 renal cell carcinoma (RCC), with a 63% response rate and 18.5-month median progression-free survival (PFS) reported in an expansion cohort of the STELLAR-002 study (NCT05176483).

“Zanzalintinib with nivolumab demonstrated promising clinical activity and tolerability in patient with first-line stage 4 RCC. Zanzalintinib in combination with immune checkpoint inhibitors, whether it's doublet or triplet, was shown to be safe and tolerable in patients with renal cell carcinoma. These encouraging preliminary clinical activity and acceptable tolerability support the ongoing studies of zanzalintinib plus immune checkpoint inhibitors in solid tumors, including RCC,” said presenting author Jad Chahoud, MD, MPH, of Moffitt Cancer Center in Tampa, Florida, at the 

2025 American Society of Clinical Oncology (ASCO) Annual Meeting

In his presentation, Chahoud explained that in previously reported data from the phase 1 STELLAR-001 study, single-agent zanzalintinib was associated with tolerability and promising antitumor activity in patients with heavily pretreated advanced clear cell renal cell carcinoma.

In addition, “Zanzalintinib activity could potentially be augmented when combined with the PD-1 inhibitor nivolumab and the LAG-3 inhibitor relatilmab, which together restore T-cell activation and result in increased antitumor activity,” the investigators wrote.

For the study presented at ASCO 2025, patients had to be at least 18 years of age with unresectable advanced or metastatic RCC with a clear cell component, all IMDC risk groups, with no prior systemic anticancer therapy for RCC (prior non-VEGF[R]-targeted adjuvant or neoadjuvant therapy was allowed if disease recurrence had taken place 6 months following the last dose). Patients were sequentially assigned to receive zanzalintinib 100 mg orally once daily plus nivolumab 480 mg intravenously (IV) once every 4 weeks or zanzalintinib 100 mg orally once daily plus nivolumab/relatlimab 480/480 mg (IV) once every 4 weeks (fixed-dose combination). The primary end points were incidence and severity of adverse events (AEs) and objective response rate (ORR) per RECIST v1.1. The secondary end point was PFS per RECIST v1.1.

“Forty patients were enrolled in each arm in this non-randomized controlled trial. Therefore, you would expect some differences in each arm. Nevertheless, both arms were reflective of patients that we see in daily practice with RCC, with around 25% of the patient population falling under the favorable IMDC risk group, and 75% falling under the intermediate- to poor-risk group,” Chahoud said.

Median follow-up was 20.1 months (range, 17.7-26.7 months) in the zanzalintinib plus nivolumab arm and 15.9 months (range, 11.3-17.3 months) in the zanzalintinib plus nivolumab/relatlimab arm. Fifteen (38%) patients in the zanzalintinib plus nivolumab arm were continuing any study treatment at data cut-off vs 16 (40%) patients in the zanzalintinib plus nivolumab/relatlimab arm. 

The most common reason for treatment discontinuation was radiographic progression, reported in 13 (33%) patients in the zanzalintinib plus nivolumab arm and 9 (23%) patients in the zanzalintinib plus nivolumab/relatlimab arm. This was followed by any treatment-emergent AE, occurring in 10 (25%) patients in the zanzalintinib plus nivolumab arm and 14 (35%) patients in the zanzalintinib plus nivolumab/relatlimab arm. 

In addition, discontinuation due to an AE related to study treatment occurred in 3 (8%) patients in the zanzalintinib plus nivolumab arm and 8 (20%) patients in the zanzalintinib plus nivolumab/relatlimab arm. Discontinuation due to withdrawal of consent other than an AE occurred in 1 (3%) patient in the zanzalintinib plus nivolumab arm and 1 (3%) patient in the zanzalintinib plus nivolumab/relatlimab arm. Discontinuation due to physician decision occurred in 1 (3%) patient in the zanzalintinib plus nivolumab arm and 0 patients in the zanzalintinib plus nivolumab/relatlimab arm.

ORR in the zanzalintinib plus nivolumab arm was 63% (95% CI: 46-77) vs 40% (95% CI: 25-57) in the zanzalintinib plus nivolumab/relatlimab arm. Three (8%) patients in the zanzalintinib plus nivolumab arm had a confirmed complete response compared with 1 (3%) patient in the zanzalintinib plus nivolumab/relatlimab arm. Twenty-two (55) patients in the zanzalintinib plus nivolumab arm had a confirmed partial response compared with 15 (38%) patients in the zanzalintinib plus nivolumab/relatlimab arm. Disease control rate was 90% (95% CI: 76-97) in both arms. 

Median duration of response (DOR) was not estimable in both arms, whereas 12-month DOR was 73.4% (50.0-87.1) in the zanzalintinib plus nivolumab arm compared with 74.1% in the zanzalintinib plus nivolumab/relatlimab arm. Median time to objective response was 2.1 months (range, 1.7-11.0 months) in the zanzalintinib plus nivolumab arm compared with 3.6 months (range, 1.7–12.8).   

Median PFS was 18.5 months (95% CI: 9.5-not estimable) in the zanzalintinib plus nivolumab arm and 13.0 months (95% CI: 7.4-not estimable) in the zanzalintinib plus nivolumab/relatlimab arm. Six-month PFS was 83.4% (95% CI: 66.8-92.2) in the zanzalintinib plus nivolumab arm compared with 80.4% (95% CI: 63.1-90.2) in the zanzalintinib plus nivolumab/relatlimab arm. Twelve-month PFS was 64.4% (95% CI: 45.7-78.1) in the zanzalintinib plus nivolumab arm compared with 58.4% (95% CI: 39.9-73.0) in the zanzalintinib plus nivolumab/relatlimab arm.

Regarding safety, median exposure time for zanzalintinib plus nivolumab was 16.1 months (range, 0.5-24.8 months) compared with 10.9 months (range, 0.5-17.1 months) in the zanzalintinib plus nivolumab/relatlimab arm. Treatment-emergent AEs of any grade or grade 3-4 were observed in 40 and 33 patients in the zanzalintinib plus nivolumab arm and in 40 and 32 patients in the zanzalintinib plus nivolumab/relatlimab arm.

“I want to bring to your attention that we only had 2 patients in each arm that had grade 4 treatment-related adverse events,” Chahoud said.

“In conclusion, zanzalintinib plus nivolumab showed promising clinical activity and tolerability, with an overall response rate of 63%, a disease control rate of 90%, and a median PFS of 18.5 months. In this nonrandomized clinical trial, the addition of relatlimab did not appear to improve objective response rate, nor median PFS. Zanzalintinib in combination with immune checkpoint inhibitor, either in doublet or triplet, was safe and tolerable. This encouraging clinical activity and tolerability supports the ongoing investigation of zanzalintinib in combination with immune checkpoint inhibitors,” Chahoud said.

1.Chahoud J, McGregor B, Reig O, et al. Zanzalintinib (zanza) + nivolumab (nivo) ± relatlimab (rela) in patients (pts) with previously untreated clear cell renal cell carcinoma (ccRCC): Results from an expansion cohort of the phase 1b STELLAR-002 study. 

. 2025;43(suppl 17):4515. doi:10.1200/JCO.2025.43.16_suppl.4515

2. Pal S. Zanzalintinib (XL092) in Clear Cell Renal Cell Carcinoma (ccRCC): Results from STELLAR-001. Presented at: 2023 International Kidney Cancer Symposium. November 9-11, 2023; Nashville, TN.

3. Hofmann M, Thimme R, Schamel WW. PD-1 and LAG-3: synergistic fostering of T cell exhaustion. 

. 2024;9(1):291. doi:10.1038/s41392-024-02000-1

The combination of zanzalintinib and nivolumab demonstrated significant efficacy and manageable safety in untreated stage 4 renal cell carcinoma, achieving a 63% response rate and 18.5-month median progression-free survival. The study involved patients with advanced or metastatic RCC, with treatments including zanzalintinib plus nivolumab or zanzalintinib plus nivolumab/relatlimab. The addition of relatlimab did not enhance the objective response rate or median PFS. The treatment was well-tolerated, with low incidence of severe adverse events, supporting further investigation of zanzalintinib with immune checkpoint inhibitors.

ORR in the zanzalintinib plus nivolumab arm was 63% (95% CI: 46-77) vs 40% (95% CI: 25-57) in the zanzalintinib plus nivolumab/relatlimab arm. 

Zanzalintinib plus nivolumab shows safety, efficacy for stage 4 RCC

Data from the phase 3 AMPLITUDE trial (NCT04497844) showed that adding niraparib (Zejula) to abiraterone acetate (Zytiga) plus prednisone (AAP) led to a statistically significant improvement in radiographic progression-free survival (rPFS) vs placebo plus AAP in patients with metastatic castration sensitive prostate cancer (mCSPC) and homologous recombinant repair (HRR) gene mutations.

 in Chicago, Illinois, suggest that the greatest rPFS benefit with the niraparib regimen is in those with 

Overall, the addition of niraparib to AAP was shown to reduce the risk of radiographic progression or death by 37% among patients in the intent-to-treat population (HRR mutations) and by 48% in patients with 

Among those with HRR mutations (ITT), the median rPFS was not met in the niraparib plus AAP arm, compared with 29.5 months in the placebo plus AAP arm (HR, 0.63; 95% CI, 0.49 to 0.80; 

 = .0001). In those with BRCA mutations, the median rPFS was not reached in the niraparib plus APP arm vs 26 months in the placebo plus APP arm (HR, 0.52; 95% CI, 0.37 to 0.72; 

Gerhardt Attard, MD, FRCP, PhD, who presented results at ASCO, noted during the presentation, “AMPLITUDE met its primary end point of radiographic progression free survival. This makes it the first trial to show efficacy for the combination of inhibition of PARP and the androgen receptor pathway in metastatic castration-sensitive prostate cancer with alterations in genes involved in homologous recombination repair, with greatest benefit apparent in patients with 

In total, the AMPLITUDE trial enrolled 696 patients who were randomly assigned to receive 200 mg niraparib plus 1000 mg abiraterone acetate plus 5 mg prednisone once daily (n = 348) or to matched placebo plus 1000 mg abiraterone acetate plus 5 mg prednisone once daily. Patients in both arms were allowed to receive androgen deprivation therapy for up to 6 months.

Participants were eligible for enrollment in the study if they had an alteration in at least 1 HRR eligible gene, which included: 

. Patients also needed to have an ECOG performance score between 0 and 2.

The trial’s primary end point is rPFS. Key secondary end points include time to symptomatic progression, overall survival (OS), and safety.

Additional data from the trial showed that the benefit of niraparib to APP was generally consistent across all pre-specified subgroups.

Attard noted, “There are a couple of subgroups that have small numbers of events, notably patients presenting with metachronous disease and the subgroups split by geographical region.”

The addition of niraparib also reduced the risk of symptomatic progression by 50% in the ITT population (HR, 0.50; 95% CI, 0.36 to 0.69; 

 < .0001) and 56% in the BRCAm cohort (HR, 0.44; 95% CI, 0.29 to 0.68; 

 = .0001). At the time of data report, the median time to symptomatic progression was not reached in either arm in either the ITT population or in the BRCAm population.

Attard also reported, “At this first interim analysis for overall survival, we have about 50% of the number of deaths that will be required for final analysis, but estimates favor the addition of niraparib [to] AAP.”

Overall, the addition of niraparib to AAP was shown to reduce the risk of death by 21% in the HRRm population (HR, 0.79; 95% CI, 0.59 to 1.04; 

 = .10) and 25% in the BRCAm population (HR, 0.75; 95% CI, 0.51 to 1.11; 

, there were 7 other HRR genes that allowed patients to be eligible for the trial,” Attard added. “Gene subgroups are small and were not pre-powered for formal analysis, but you'll appreciate probable heterogeneous effect across these single gene groups. I would expect that in the future, combinations with other trials, possibly using meta-analysis approaches, will give us greater certainty for the sensitivity of individual gene groups to PARP inhibition in this disease setting.”

The majority of patients who discontinued treatment due to progression went on to receive a subsequent therapy. There were comparable rates of subsequent therapy between the 2 arms with the exception of subsequent PARP inhibition, reported in 11% of patients in the niraparib arm vs 36% of patients in the placebo arm.

Regarding safety, grade 3 to 4 treatment-emergent adverse events (AEs) were reported in 75% of patients in the niraparib arm vs 59% in the placebo arm. The investigators also noted a less than 5% increase in the rate of discontinuation due to toxicity with niraparib vs placebo (15% vs 10%, respectively).

The most common grade 3 or higher AE was anemia, reported in 29% of patients in the niraparib arm vs 5% of patients in the placebo arm. Grade 3 or higher hypertension was also reported in 27% of patients in the niraparib arm vs 18% of patients in the placebo arm.

Other common AEs of any grade included constipation (35% vs 16%), nausea (31% vs 14%), fatigue (26% vs 18%), and arthralgia (21% vs 21%) in the niraparib vs placebo arms, respectively.

Based on these data, the authors concluded, “AMPLITUDE supports early genomic testing and niraparib plus AAP as a new treatment option for patients with mCSPC and HRR gene alterations.”

1. Attard G, Agarwal N, Graff J, et al. Phase 3 AMPLITUDE trial: Niraparib (NIRA) and abiraterone acetate plus prednisone (AAP) for metastatic castration-sensitive prostate cancer (mCSPC) patients (pts) with alterations in homologous recombination repair (HRR) genes. 

. 2025;43 (suppl 17; abstr LBA5006). Doi: 10.1200/JCO.2025.43.17_suppl.LBA5006

The phase 3 AMPLITUDE trial demonstrated that adding niraparib to abiraterone acetate plus prednisone significantly improved radiographic progression-free survival in patients with metastatic castration-sensitive prostate cancer and homologous recombinant repair gene mutations. The greatest benefit was observed in patients with BRCA mutations. The trial met its primary endpoint, showing a 37% risk reduction in radiographic progression or death in the intent-to-treat population and 48% in the BRCA mutation cohort. Safety data indicated higher rates of grade 3-4 adverse events in the niraparib arm, with anemia being the most common.

“AMPLITUDE supports early genomic testing and niraparib plus AAP as a new treatment option for patients with mCSPC and HRR gene alterations," the authors wrote.

Adding niraparib to AAP extends rPFS in HRR-positive mCSPC

Five-year data from the phase 3 ARCHES trial (NCT02677896) showed that enzalutamide (Xtandi) plus androgen deprivation therapy (ADT) continued to provide a substantial and durable benefit in overall survival (OS) vs placebo plus ADT in patients with metastatic hormone-sensitive prostate cancer (mHSPC).

At a median follow-up of 61.4 months, enzalutamide plus ADT was associated with a 30% reduction in the risk of death vs placebo plus ADT (HR, 0.7; 95% CI, 0.58 to 0.85; 

 = .001). The probability of survival at 5 years was 65.5% (95% CI, 61.2 to 69.5) in the treatment arm vs 53.4% (95% CI, 48.5 to 57.9) in the control arm.

The phase 3 ARCHES trial demonstrated that enzalutamide combined with androgen deprivation therapy (ADT) significantly improves overall survival (OS) in patients with metastatic hormone-sensitive prostate cancer (mHSPC) compared to placebo plus ADT. At a median follow-up of 61.4 months, enzalutamide plus ADT reduced the risk of death by 30%. The 5-year survival rate was 66.5% for the treatment group versus 53.4% for the control group. The survival benefit was consistent across various subgroups, including those with high-volume disease and prior docetaxel use, despite increased treatment-emergent adverse events.

According to the authors, these data continue to support enzalutamide plus ADT as a standard-of-care for patients with mHSPC. 

Raymond A. Costabile, MD

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