RUBRACA® (rucaparib) is a flexible, targeted, effective, and supportive PARPi that targets BRCA-mutated mCRPC and can be used after ANY ARPI and taxane-based chemotherapy.4*† Learn more about RUBRACA at RubracaProstateHCP.com.
*
Patients should also receive a GnRH analog concurrently or should have had bilateral orchiectomy.4
†
Demonstrated improvements in multiple efficacy outcomes: confirmed overall response rate (ORR) by independent radiology review (IRR), 46% (95% CI, 35%-57%); median duration of response (DOR) by IRR, 15.5 months (95% CI, 6.4-not reached).5
RUBRACA is indicated for patients previously treated with any androgen receptor-directed therapy and a taxane-based chemotherapy.4
Myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) occur in patients treated with RUBRACA, and are potentially fatal adverse reactions.
For Important Safety Information and full Prescribing Information for RUBRACA, visit RubracaProstateHCP.com.
ELIGARD® (leuprolide acetate) is a GnRH agonist used as a foundation of treatment for advanced prostate cancer that provides proven efficacy and safety, customizable dosing, extended control, and unmatched access and support so you and your patients can feel empowered while on ADT.6-12
Learn more about ELIGARD at ELIGARDhcp.com.
ELIGARD for injectable suspension is a gonadotropin-releasing hormone (GnRH) agonist indicated for the treatment of advanced prostate cancer.6
ELIGARD may impair fertility in males of reproductive potential.
For Important Safety Information and full Prescribing Information for ELIGARD, visit ELIGARDhcp.com.
Different treatments can be used depending on the progression of aPC, and each class of therapy provides unique therapeutic benefits and risks for patients.
Select a treatment listed below to learn more about what it is and when it may be used.
Immunotherapies are advanced medicines that leverage the patient’s own immune system to combat cancer cells, and are a treatment option for those with mCRPC.
PARPis are targeted medicines that block cancer cells from repairing their own DNA, causing apoptosis and cell death of the cancer cells
RUBRACA® (rucaparib) is a flexible, targeted, effective, and supportive PARPi that targets BRCA-mutated mCRPC and can be used after ANY ARPI and taxane-based chemotherapy.*† Learn more about RUBRACA at RubracaProstateHCP.com.
*
Patients should also receive a gonadotropin-releasing hormone (GnRH) analog concurrently or should have had bilateral orchiectomy.9
†
Demonstrated improvements in multiple efficacy outcomes: confirmed overall response rate (ORR) by independent radiology review (IRR), 46% (95% CI, 35%-57%); median duration of response (DOR) by IRR, 15.5 months (95% CI, 6.4-not reached).5
RUBRACA is indicated for patients previously treated with any androgen receptor-directed therapy and a taxane-based chemotherapy.4
Myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) occur in patients treated with RUBRACA, and are potentially fatal adverse reactions.
For Important Safety Information and full Prescribing Information for RUBRACA, visit RubracaProstateHCP.com.
Chemotherapies are drugs that directly kill or slow down the growth of cancer cells.
Radioligand therapy is a category of targeted cancer treatment that uses radioactive isotopes (called radioligands) to precisely deliver radiation to cancer cells while minimizing off-target damage to healthy tissues for patients with mCRPC.
ADT is used as the foundation of therapy for advanced prostate cancer and can be given during the entirety of prostate cancer treatment. ADT, or hormone therapy, functions by reducing levels of male sex hormones, called androgens. Over time, other types of therapies can be added to a patient’s treatment plan in addition to ADT.
Luteinizing hormone-releasing hormone (LHRH) and gonadotropin-releasing hormone (GnRH) therapies
ELIGARD may impair fertility in males of reproductive potential.
When using ADTs, assess T regularly to maintain T suppression ≤20 ng/dL2. With ADTs, disease can continue to progress despite T suppression, so it’s important to identify CRPC early. ADTs can also cause many different side effects due to suppressing T, so combinatorial therapeutic strategies will need to be implemented and early mitigation of side effects should be completed to maintain the patient’s quality of life.20
A 60-year-old man diagnosed with localized prostate cancer was initially treated with radical prostatectomy, followed by external radiation therapy a year ago. His PSA was initially undetectable but has now started to rise to 0.2 ng/mL. What next steps would you follow?
A 65-year-old man was diagnosed with metastatic hormone sensitive prostate cancer. Imaging revealed 2 bone metastases and no visceral involvement and his PSA level was 120 ng/mL. What treatment approach would you follow?
A 70-year-old male was diagnosed with locally advanced prostate cancer 3 years ago, was treated with radical prostatectomy and radiation therapy. Due to biochemical recurrence, he was started on ADT treatment. After a year on ADT, his PSA levels began to rise again, while at castration T levels (20 ng/dL). Sensitive imaging did not reveal any metastases, indicating nmCRPC. How would you approach next steps in his treatment?
A 75-year-old male was initially diagnosed with mCSPC two years ago. He was treated with the triplet combination of ADT, docetaxel and abiraterone/prednisone. He responded to treatment and his PSA levels decreased significantly. However, over the last 6 months, his PSA levels have been rising while maintaining castrate T levels and imaging showed new bone metastases, but no visceral organ involvement, indicating progression to mCRPC. How would you approach further treatment?