Combination immunotherapy for metastatic prostate cancer shows promise
21 May 2021
A combination of two antibody therapeutics - nivolumab and ipilimumab - has achieved the best response yet seen in the treatment of metastatic prostate cancer, according to early results from a UCL-led Phase II trial. 

Prostate cancer is the second most common cancer affecting men globally and the fourth most common cancer overall. Many patients with prosate cancer do not require treatment or are successfully treated, but a proportion will experience spread to other organs, which is called metastatic prostate cancer. Metastatic prostate cancer can be controlled with hormone therapy but invariably this stops working, a state known as metastatic castration-resistant prostate cancer’ (mCRPC). Despite recent advances in treatments for mCRPC the disease is incurable and has a prognosis of only 2-3 years.

The ongoing phase II NEPTUNES trial is exploring whether treatments that boost the body’s immune system (called checkpoint inhibitors) can provide benefit for patients with mCRPC. In April 2021, Dr Mark Linch from the UCL Cancer Institute, principal investigator of the NEPTUNES trial, presented preliminary data from the trial at the American Association for Cancer Research (AACR) virtual annual meeting.

Checkpoint inhibitors (CPIs) have demonstrated deep and durable responses for a range of cancers but there has been limited success in prostate cancer so far. This may be because prostate cancers are difficult for the immune system to see and hard to access due to chemical and physical barriers around the tumour.  The NEPTUNES trial is testing whether a subgroup of patients which have either certain defects in the mechanism of DNA repair (making them more visable to the immune system) or already have immune cells within the tumour may render them particularly sensitive to these treatments. This combination of features has been coined the immunogenic signature (ImS+).

Nivolumab and ipilimumab are given for up to four cycles together, with nivolumab alone then used for up to a year after a 6-week gap. Cancer induces an unwanted break mechanism on the cancer killing T-cells (immune cell) enabling further cancer growth. This break can be blocked with CPIs activating the T-cells, which hopefully then find, kill and keep remembering to kill the cancer.  Nivolumab blocks the PD-1 break and ipilimumab blocks the CTLA-4 break.  

Initial data on 35 patients with the appropriate immunogenic signature showed that 10 patients achieved the pre-specified set of criteria for a positive response (28.6% response rate). Although the data do not yet provide definitive evidence of a treatment effect, this is the highest response rate yet for immunotherapy in mCRPC and several of the responding patients have had a durable response.

“These are the best results seen with this kind of immunotherapy for metastatic prostate cancer, although it is still early days. We believe the further study of nivolumab and ipilimumab in biomarker-selected patients with metastatic castration-resistant prostate cancer is warranted,” said Dr Mark Linch, Associate Professor (UCL Cancer Institute), Consultant Medical Oncologist (UCLH) and chief investigator of the trial. 

Encouragingly, the study has identified features associated with a positive response to the combination therapy, such as the presence of mutated BRCA1 or BRCA2 genes or high inflammatory infiltrate within the tumour. This may provide a way to identify patients most likely to respond to the therapy.

However, not all patients managed to complete the treatment, sometimes due to side effects from the treatment. The NEPTUNES trial is continuing to recruit men with mCRPC but using a better tolerated dose schedule which will hopefully provide even more benefit to patients. 

The study is run by the CR UK & UCL Cancer Trials Centre and sponsored by UCL.

Contact Us
Cancer Research UK & UCL Cancer Trials Centre
University College London
90 Tottenham Court Road

View map
+44 (0)20 7679 9898 (General CTC Enquiries)
020 7679 9899
University College London, Gower Street, London, WC1E 6BT +44 (0)20 7679 2000

Copyright © 2024 UCL | Disclaimer | Freedom of Information | Accessibility | Privacy | Cookies | Contact Us