Niraparib shows significant promise in the treatment of advanced ovarian cancer patients with poor treatment options


Encouraging results have emerged from a Phase3 clinical trial that investigated the efficacy of Niraparib, an orally administered poly ADP ribose polymerase (PARP) inhibitor, in patients with newly diagnosed advanced ovarian cancer who were at high risk for relapse (González-Martín et al, 2019). In such patients, Niraparib maintenance treatment resulted in significantly increasing progression-free survival (the time when the cancer did not progress further in the patient), compared to those treated with a placebo. Niraparib could consequently become an integral part in the arsenal against advanced ovarian cancer.

Ovarian cancer is characterised with the poorest survival rate among all gynaecological cancers resulting in 152,000 deaths worldwide each year. The main treatments for ovarian cancer are surgery, and combination chemotherapy with platinum and paclitaxel. However, up to 85% of the patients with advanced ovarian cancer have a relapse on completing chemotherapy. Even when treatments exist, there are safety concerns, or only a subset of patients is targeted. Therefore, there remains an unmet medical need for the vast majority of patients with advanced ovarian cancer.

The protein, poly ADP ribose polymerase (PARP), plays a crucial role in DNA repair. PARP helps repair damaged cells by mending single-strand breaks in the DNA. PARP inhibitors halt DNA repair in cancer cells leading to cell death. Previous clinical studies have focussed on PARP inhibitors in tumours with BRCA mutations as fault in this gene too results in impaired DNA repair. The rationale is that blocking PARP with a PARP inhibitor in such a context would prevent the cells from repairing themselves leading to cell death. Therefore, clinical trials had been conducted in selected patient populations. Niraparib, had been previously shown to be significantly effective in ovarian cancer patients with BRCA mutations leading to its regulatory approval. However, recent studies as evident in the PRIMA trial show that Niraparib is effective in ovarian cancer patients regardless of BRCA mutations.

The latest clinical trial involved 733 ovarian cancer patients. Patients were at  Stages III or IV who have advanced disease and  considered to have incurable disease with chemotherapy alone, including those who had tumors with homologous-recombination deficiency (with either mutated or unmutated BRCA) and those with homologous-recombination proficiency. All patients had been previously treated with platinum-based chemotherapy and had shown response to it. Patients were randomised and treated with Niprarib or a placebo.

-The median progression-free survival in patients having tumours with homologous-recombination deficiency, was 21.9 months in the Niraparib group which was significantly longer than in the placebo group (10.4 months).
Within the population with homologous-recombination deficiency, the median duration of progression-free survival in the subgroup with BRCA mutations was 22.1 months in the niraparib group and 10.9 months in the placebo group. In the subgroup without BRCA mutations progression-free survival was  19.6 months with niraprib and 8.2 months on placebo

-In the subgroup of patients with homologous-recombination proficiency, the median duration of progression-free survival was 8.1 months in the niraparib group and 5.4 months in the placebo group.
In patients with advanced ovarian cancer in other subgroups with a poor prognosis, including in those who received neoadjuvant chemotherapy, the median duration of progression-free survival 13.9 (Niraparib) vs. 8.2 months (placebo).

In the overall population, the progression-free survival was 13.8 months in niraparib group and 8.2 months with placebo.

References: González-Martín A et al, Niraparib in Patients with Newly Diagnosed Advanced Ovarian Cancer,  N Engl J Med. 2019 Sep 28.


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