Lynparza (olaparib) vs Orgovyx (relugolix)

Lynparza (olaparib) vs Orgovyx (relugolix)

Lynparza (olaparib) is a targeted therapy known as a PARP inhibitor, primarily used for treating certain types of breast, ovarian, fallopian tube, or peritoneal cancers in patients with specific genetic mutations (BRCA1/2 or other homologous recombination repair mutations). Orgovyx (relugolix) is an oral gonadotropin-releasing hormone (GnRH) receptor antagonist indicated for the treatment of advanced prostate cancer. When deciding between these medications, it is crucial to consider the type of cancer being treated, as Lynparza is not indicated for prostate cancer, and Orgovyx is not used for the cancers treated by Lynparza, making the choice dependent on the specific diagnosis and genetic background of the patient.

Difference between Lynparza and Orgovyx

Metric Lynparza (olaparib) Orgovyx (relugolix)
Generic name Olaparib Relugolix
Indications Ovarian, breast, pancreatic, and prostate cancer Advanced prostate cancer
Mechanism of action Poly (ADP-ribose) polymerase (PARP) inhibitor Gonadotropin-releasing hormone (GnRH) receptor antagonist
Brand names Lynparza Orgovyx
Administrative route Oral Oral
Side effects Anemia, nausea, fatigue, vomiting, neutropenia, respiratory infections Hot flushes, increased glucose, increased triglycerides, musculoskeletal pain, decreased libido
Contraindications Hypersensitivity to olaparib, breastfeeding Hypersensitivity to relugolix, pregnancy
Drug class Antineoplastic agent Gonadotropin-releasing hormone antagonist
Manufacturer AstraZeneca and Merck & Co. (MSD outside the US and Canada) Myovant Sciences, Inc.

Efficacy

Lynparza (Olaparib) Efficacy in Prostate Cancer

Lynparza, also known by its generic name olaparib, is a PARP inhibitor that has shown efficacy in treating prostate cancer in certain contexts. Specifically, it has been approved for use in men with metastatic castration-resistant prostate cancer (mCRPC) who have deleterious or suspected deleterious germline or somatic homologous recombination repair (HRR) gene mutations. These mutations must be detected by an FDA-approved test after the disease has progressed following prior treatment with enzalutamide or abiraterone. In clinical trials, olaparib has demonstrated the ability to significantly delay disease progression and improve overall survival rates in this subset of patients.

The efficacy of Lynparza in prostate cancer was evaluated in the PROfound study, a Phase 3 randomized clinical trial that specifically looked at patients with HRR gene-mutated mCRPC who had progressed on prior next-generation hormonal agent (NHA) treatment. The results indicated that Lynparza significantly improved radiographic progression-free survival (rPFS) compared to the control group receiving NHA. Additionally, there was an observed improvement in overall survival, although this outcome was not the primary endpoint of the trial.

Orgovyx (Relugolix) Efficacy in Prostate Cancer

Orgovyx, with the generic name relugolix, is an oral gonadotropin-releasing hormone (GnRH) receptor antagonist indicated for the treatment of adult patients with advanced prostate cancer. As a GnRH antagonist, relugolix works by rapidly reducing testosterone levels, which is a critical aspect of managing advanced prostate cancer. Clinical studies have shown that Orgovyx is effective in achieving and maintaining castrate levels of testosterone in men with advanced prostate cancer.

The efficacy of Orgovyx was primarily demonstrated in a pivotal Phase 3 trial known as the HERO study. In this trial, patients with advanced prostate cancer were treated with Orgovyx and were compared to those receiving leuprolide, a commonly used injectable GnRH agonist. The results showed that Orgovyx was superior in achieving sustained testosterone suppression to castrate levels after 48 weeks of treatment. Furthermore, Orgovyx demonstrated a rapid onset of action, with a significant proportion of patients reaching castrate levels of testosterone on day 4 of treatment, which can be particularly beneficial for patients requiring quick testosterone suppression.

Regulatory Agency Approvals

Lynparza
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Orgovyx
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Lynparza or Orgovyx today

If Lynparza or Orgovyx are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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