Vigil Immunotherapy Prolongs RFS as Frontline Maintenance Treatment in Ovarian Cancer

Rodney P. Rocconi, MD

Rodney P. Rocconi, MD

Relapse-free survival (RFS) was prolonged in patients with stage III/IV ovarian cancer who received frontline maintenance treatment with Vigil immunotherapy compared with placebo. This was especially true for patients withBRCA1/2 wild-type disease, according to results from the phase II VITAL study.

Results showed that the median RFS favored the Vigil arm over placebo in the overall patient population (n = 91) at 12.6 months versus 8.4 months, respectively (HR, 0.69;P= .065).

However, when stratified byBRCAstatus, the RFS improvement was found to be statistically significant in the BRCA1/2wild-type patients (n = 67) in the Vigil arm at 19.4 months compared with 14.8 months in the control arm (HR, 0.459;P= .007) from time of randomization. Moreover, the median overall survival (OS) was not reached with Vigil and was 41.4 months with placebo from time of randomization (HR, 0.417;P= .020).

Having the first maintenance therapy that is specific to [BRCA1/2] wild-type patients that shows a survival benefit both in [relapse]-free and overall survival is significant in my mind,lead study author Rodney P. Rocconi, MD, Elsie Colle Chair of Oncology Research, associate director of Clinical Research, and professor of gynecologic oncology at USA Mitchell Cancer Institute, said in an interview withTargeted Oncology.

The second thing is that we're getting almost to the point to where we thought immunology would not work in ovarian cancer. This vaccine shows that by a different approach, or a different set of methods, that the door is not shut on immunotherapy in ovarian cancer; there are ways to go about this, added Rocconi, who was scheduled to present these data during the 2020 SGO Annual Meeting.

The overall prognosis for patients with advanced epithelial ovarian cancer is poor, and those with BRCA1/2 wild-type disease, which Rocconi said comprises 85% of all patients with ovarian cancer, have become an unmet need, he explained. Additionally, elevated TGF-β expression is found to also correlate with poor prognosis in this disease.

Vigil immunotherapy is defined as an autologous tumor cell vaccine that is comprised from autologous harvested tumor tissue that is transfected with a DNA plasmid encoding GMCSF and bi-shRNA-furin, which leads to control of TGF-β expression.

“One thing [about this vaccine, which makes it] a little bit different is that it's not really a global, immunologic therapy, but it's very targeted, and very specific,” said Rocconi. “We are actually harvesting a patient’s cancer at the time of surgery prior to chemotherapy, and we create vaccines to the neoantigens that are on that cancer cell. By doing that, the vaccine is attracted or targeted to that own individual patient’s cancer cells.”

In the double-blind, placebo-controlled, randomized VITAL trial (NCT02346747), investigators sought to evaluate whether a frontline maintenance approach with Vigil would improve RFS in this patient population. Investigators randomized 91 patients with advanced-stage ovarian cancer who achieved complete clinical response to frontline surgery and chemotherapy to receive Vigil at 1 x 10e7 cells/ml (n = 46) or placebo (n = 45) monthly for ≤12 doses.

To be eligible for enrollment, patients must have had stage IIIb, IIIc or IV high-grade papillary serous/clear cell/endometrioid ovarian, fallopian tube or primary peritoneal cancer; could not have received prior chemotherapy or investigational agents before tissue acquisition for Vigil manufacturing; could not have had another malignancy; had an ECOG performance status of 0 to 2 prior to diagnostic laparoscopy or debulking laparotomy; and must have had no prior history of hypersensitivity reactions with taxanes or platinum-based therapy.

ThroughBRCA1/2testing, it was determined that 74% of patients were BRCA1/2wild-type and 26% harbored BRCA1/2mutations. The key endpoints were RFS, safety, and proportion of recurrences. The median time from surgery to randomization was 6.9 months in the Vigil arm versus 6.6 months in the control group.

Moreover, additional findings showed that in the overall cohort, recurrence were observed in 54% of Vigil-treated patients compared with 76% of patients who received placebo (chi-squareP= .014). When stratified by BRCAstatus, 51% of Vigil-treated patients with BRCA1/2wild-type disease experienced disease relapse versus 79% of BRCA1/2wild-type patients who received placebo (chi-square P= .023).

However, in theBRCA1/2-mutant population, there was no benefit observed with the use of Vigil.

Additionally, 23% and 46% of patients on the Vigil and placebo arms had died, respectively. Regarding safety, there was no additional toxicity in the Vigil arm compared with the control group. Grade 2/3 adverse events (AEs) occurred in 8% of Vigil-treated patients compared with 18% of those in the control group. The most common AEs of this severity in the Vigil arm was bone pain and fatigue, while nausea and musculoskeletal pain were most common in the placebo arm. No grade 4/5 AEs were observed.

“If we are able to move this forward and essentially get an indication for this from the FDA, this would be the first agent that specifically benefits theBRCA1/2wild-type patient to have fewer recurrences and hopefully longer lives,” Rocconi concluded.

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Reference:

Rocconi RP, Barve M, Botts-ford-Miller JN, et al. Randomized double-blind placebo controlled trial of primary maintenance vigil immunotherapy (VITAL study) in stage III/IV ovarian cancer: Efficacy assessment in BRCA1/2-wt patients. Data made available as part of the virtual platform for the SGO 2020 Annual Meeting. Abstract LBA7.