Expert Discusses Bipolar Androgen Therapy Plus PARP Inhibition for Castration-Resistant Prostate Cancer

Video

CancerNetwork® spoke with Michael Schweizer, MD, at the 2021 ESMO Congress about his research into the combination of olaparib plus bipolar androgen therapy for patients with castration-resistant prostate cancer.

At the 2021 European Society for Medical Oncology Congress, CancerNetwork® spoke with Michael Schweizer, MD, assistant professor in the Division of Medical Oncology at the University of Washington School of Medicine and associate professor of the Clinical Research Division at Fred Hutchinson Cancer Research Center, about his research on the combination regimen of olaparib (Lynparza) plus bipolar androgen therapy (BAT) for patients with castration-resistant prostate cancer (CRPC).

The single-center, phase 2 study (NCT03516812) enrolled 36 patients (median age, 70 years; range, 51-88) with CRPC who received either prior abiraterone acetate (Zytiga) and/or enzalutamide (Xtandi) to receive olaparib at 300 mg orally twice daily plus BAT. Almost half (47%) of patients had a PSA50 response, defined as a 50% or greater decline in their PSA level. At a median follow-up of 22.7 months, the median progression-free survival (PFS) was 12.6 months.

Schweizer said this approach is not ready for the clinic yet, but it holds promise for this group of patients being treated by a medical oncologist.

Transcript:

I don't think this is necessarily going to shift the standard of care right now because it’s a relatively small phase 2 trial. You know, hypothetically, if it turned out that this combination was active, they could prove it in a randomized trial, and it became a standard of care, this would probably still fall predominantly on medical oncology to treat these patients since you're talking about utilizing drugs like PARP inhibitors, which tend to be mostly utilized in the medical oncology field.

In theory, I could see if this really panned out to be a therapy that was effective for an unselected population that perhaps it would start going back towards urologists utilizing it more since it doesn’t require sort of advanced genomic testing. For now, it’s probably not going to necessarily be something that relies heavily on a multidisciplinary approach for utilization since it’s a drug-based treatment.

Reference

Schweizer M, Gulati R, Yezefski T, et al. Bipolar androgen therapy (BAT) plus olaparib in men with metastatic castration-resistant prostate cancer (mCRPC). Presented at: 2021 European Society for Medical Oncology Congress. September 16-21, 2021. Abstract 592P

Recent Videos
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Although accuracy remains a focus in whole-body MRI testing in patients with Li-Fraumeni syndrome, comfortable testing experiences may ease anxiety.
Subsequent testing among patients in a prospective study may affirm the ability of cfDNA sequencing to detect cancers in those with Li-Fraumeni syndrome.
cfDNA sequencing may allow for more accessible, frequent, and sensitive testing compared with standard surveillance in Li-Fraumeni syndrome.
STX-478 showed efficacy in patients with advanced solid tumors regardless of whether they had kinase domain or helical PI3K mutations.
STX-478 may avoid adverse effects associated with prior PI3K inhibitors that lack selectivity for the mutated protein vs the wild-type protein.
Phase 1 data may show the possibility of rationally designing agents that can preferentially target PI3K mutations in solid tumors.
Funding a clinical trial to further assess liquid biopsy in patients with Li-Fraumeni syndrome may help with detecting cancers early across the board.
Michael J. Hall, MD, MS, FASCO, discusses the need to reduce barriers to care for those with Li-Fraumeni syndrome, including those who live in rural areas.
Related Content