New data presented at the ESMO Congress 2019 in Barcelona, Spain, show the benefit of a more intensive maintenance regimen for ovarian cancer with the PARP inhibitor olaparib added to bevacizumab, in an all-comers population, with and without a BRCA mutation. According to late breaking results of the PAOLA-1/ENGOT-ov25 trial, this approach extends progression free survival in patients with advanced ovarian cancer. (1)
Ovarian cancer is the fifth most common cancer in women and the most lethal gynaecological tumour. The majority of patients are diagnosed in an advanced stage and despite responding well to first-line treatment, usually relapse less than two years after diagnosis. Longer progression free survival after first-line therapy improves the probability of response to a new line of chemotherapy. The current standard of care for most patients with newly diagnosed advanced ovarian cancer is surgery and platinum-based chemotherapy combined with bevacizumab, followed by bevacizumab alone.
PAOLA-1/ENGOT-ov25 is the first phase III trial to examine the efficacy and safety of a PARP inhibitor with bevacizumab as first-line maintenance therapy in patients with ovarian cancer with and without a BRCA mutation. This international, academic-led trial enrolled 806 patients with stage III/IV ovarian cancer and partial or complete response to standard platinum-based chemotherapy and bevacizumab. After completing first-line chemotherapy, patients were randomly allocated 2:1 to olaparib or placebo, both on top of bevacizumab. They received olaparib for up to 24 months and bevacizumab for 15 months in total. The primary outcome was investigator-assessed progression free survival.
The median follow-up was 24 months in the olaparib arm and 22.7 months in the placebo arm. Median progression free survival was 22.1 months in the olaparib group and 16.6 months in the placebo group (hazard ratio 0.59; 95% confidence interval 0.49–0.72; p<0.0001).
“This study reports the greatest hazard ratio (0.59) and longest progression free survival we have ever seen,” said study author Prof Isabelle Ray-Coquard, Centre Leon Bérard, Université Claude Bernard, Lyon, and president of the GINECO group France. “Patient selection was not restricted by surgical outcome or BRCA mutation status, so participants represent the general population of women with advanced ovarian cancer. Previous studies of relapse have suggested benefits from combining anti-angiogenic agents and PARP inhibitors (2,3) and today’s results appear to support this. In addition, olaparib did not increase side-effects compared to placebo.”
In prespecified subgroup analyses, the progression free survival benefit of olaparib versus placebo was even more pronounced in patients with a BRCA mutation and in those with homologous recombination deficiency (HRD), with hazard ratios of 0.31 and 0.33, respectively. Median progression free survival with olaparib reached 37.2 months in patients with a BRCA mutation and in patients with HRD. “The results in HRD patients without a BRCA mutation identify, for the first time, a patient population with greater clinical benefit from olaparib when added to bevacizumab,” said Ray-Coquard.
Ray-Coquard noted that randomisation in PAOLA-1/ENGOT-ov25 started a median six weeks after the last cycle of chemotherapy, whereas most previous trials started randomisation with the first cycle of chemotherapy. “It is an important point to consider when comparing the results to other data,” she said.
Commenting on the relevance of the data, Dr Ana Oaknin, Vall d´Hebron Institute of Oncology (VHIO), Barcelona, said: “The main goal in ovarian cancer is to avoid relapse after first-line therapy because otherwise the probability of cure is quite low. The combination of bevacizumab and olaparib as maintenance therapy should become a new standard of care for patients with advanced ovarian cancer. The PAOLA-1/ENGOT-ov25 trial did not include patients with no response to first-line chemotherapy, but this is a small group. This trial is a significant step forward in treatment for these women.”
Other positive trials of PARP inhibitors in advanced ovarian cancer are presented at the ESMO Congress 2019. In the PRIMA trial, niraparib administered after completion of first-line chemotherapy significantly improved progression free survival. (4) In the VELIA/GOG-3005 trial, veliparib integrated with first-line chemotherapy then continued as maintenance treatment significantly extended progression free survival regardless of response to first-line treatment. (5)
Oaknin said these three trials and the SOLO-1 trial, (6) all integrating PARP inhibitors in first-line treatment, are a milestone for patients. “After decades studying different chemotherapy approaches, it is the first time we have meaningfully prolonged progression free survival and hopefully we will improve long-term outcome,” she said. Oaknin noted there were important differences between the two trials and PAOLA-1/ENGOT-ov25. For example, patients in PRIMA did not receive bevacizumab, were not stratified according to BRCA status, and were treated for almost three years. The VELIA trial tested veliparib concurrent with standard chemotherapy and then as maintenance therapy. “Therefore, comparisons between clinical trials should be made with caution due to their intrinsic differences,” she said.
Regarding the next priority for research in this field, Oaknin said: “The five-year overall survival for ovarian cancer is around 45% and we need strategies to improve that figure. I think the next approach is to incorporate immunotherapy as part of first-line therapy. Ongoing trials are expected to report in two to three years.”
- LBA2_PR ‘Phase III PAOLA-1/ENGOT-ov25 trial: Olaparib plus bevacizumab (bev) as maintenance therapy in patients (prs) with newly diagnosed, advanced ovarian cancer (OC) treated with platinum-based chemotherapy (PCh) plus bev‘ will be presented by Isabelle L. Ray-Coquard during the Presidential Symposium I on Saturday, 28 September, 16:30 to 18:20 (CEST) in the Barcelona Auditorium (Hall 2). Annals of Oncology, Volume 30, Supplement 5, October 2019
- Mirza MR, Åvall Lundqvist E, Birrer MJ, et al. Niraparib plus bevacizumab versus niraparib alone for platinum-sensitive recurrent ovarian cancer (NSGO-AVANOVA2/ENGOT-ov24): a randomised, phase 2, superiority trial. Lancet Oncol. 2019. pii: S1470-2045(19)30515-7. doi: 10.1016/S1470-2045(19)30515-7.
- Liu JF, Barry WT, Birrer M, et al. Overall survival and updated progression-free survival outcomes in a randomized phase II study of combination cediranib and olaparib versus olaparib in relapsed platinum-sensitive ovarian cancer. Ann Oncol. 2019;30:551–557. doi: 10.1093/annonc/mdz018.
- LBA1 ‘Niraparib treatment in patients with newly diagnosed advanced ovarian cancer (OC)‘ will be presented by A. González Martín during the Presidential Symposium I on Saturday, 28 September, 16:30 to 18:20 (CEST) in the Barcelona Auditorium (Hall 2).
- LBA3 ‘VELIA/GOG-3005: Integration of veliparib (V) with front-line chemotherapy and maintenance in women with high-grade serous carcinoma of ovarian, fallopian tube, or primary peritoneal origin (HGSC)‘will be presented by Robert L. Coleman during the Presidential Symposium I on Saturday, 28 September, 16:30 to 18:20 (CEST) in the Barcelona Auditorium (Hall 2).
- Moore K, Colombo N, Scambia G, et al. Maintenance Olaparib in Patients with Newly Diagnosed Advanced Ovarian Cancer. N Engl J Med 2018; 379:2495-2505. doi: 10.1056/NEJMoa1810858