Verzenio Approved to Treat Breast Cancer
Verzenio (abemaciclib) was granted FDA approval for certain patients with advanced or metastatic breast cancer.
Verzenio (abemaciclib) was granted FDA approval for the use in combination with Faslodex (fulvestrant) to treat patients with HR+/HER2- advanced breast cancer with disease progression following endocrine therapy. The CDK4/6 inhibitor has also been approved as a monotherapy for patients with HR+/HER2- breast cancer with metastatic disease who have previously received endocrine therapy and chemotherapy.
Support for combination indication comes from the phase 3 MONARCH 2 trial, in which adding Verzenio to Faslodex reduced the risk of disease progression or death by 45 percent versus Faslodex alone. The single-agent approval is based on the single-arm phase 2 MONARCH 1 trial, in which the median progression-free survival (PFS) in this patient population was 6 months (95 percent CI 4.2-7.5) and the median overall survival (OS) was 17.7 months.
"Verzenio provides a new targeted treatment option for certain patients with breast cancer who are not responding to treatment, and unlike other drugs in the class, it can be given as a stand-alone treatment to patients who were previously treated with endocrine therapy and chemotherapy," Richard Pazdur, M.D., director of the FDA’s Oncology Center of Excellence and acting director of the Office of Hematology and Oncology Products in the FDA’s Center for Drug Evaluation and Research, said in a statement.
In the international, double-blind phase 3 MONARCH 2 trial, 669 patients were randomized in a 2:1 ratio to Verzenio plus Faslodex (446 patients) or Faslodex plus placebo (223 patients). Patients had progressed during neoadjuvant or adjuvant endocrine therapy, within 12 months of adjuvant endocrine therapy, or during frontline endocrine treatment for metastatic disease. Individuals were excluded from enrollment if they were administered chemotherapy or more than 1 endocrine therapy in the metastatic setting.
Patient characteristics were well-balanced between the two arms. Overall, 82 percent of patients were postmenopausal, 72 percent had measurable disease, 56 percent had visceral disease and 25 percent had primary endocrine therapy resistance. About 60 percent of patients had received chemotherapy in the adjuvant or neoadjuvant setting.
Patients received 500 mg (per label) of Faslodex plus placebo or 150 mg of Verzenio twice daily. The initial Verzenio dose was 200 mg twice daily; however, the dose was amended after the first 178 patients were enrolled, due to diarrhea-related toxicity concerns. A GnRH agonist was given to pre/perimenopausal patients. The primary endpoint for the trial was PFS. Secondary endpoints included OS, response, clinical benefit rate, and safety.
Following 379 PFS events in the intent-to-treat population, the median PFS was 16.4 months in the Verzenio arm versus 9.3 months in the Faslodex -alone group. The ORRs among patients with measurable disease were 48.1 percent and 21.3 percent in the Verzenio and control arms, respectively.
The 48.1 percent ORR in the Verzenio cohort included a complete response rate of 3.5 percent. There were no complete responses in the control arm. The median duration of response was 25.6 months in the placebo arm and had not yet been reached in the Faslodex arm. The OS data are not yet mature.
The most common all-grade treatment-related AEs with the Verzenio combination versus Verzenio alone were diarrhea (86.4 percent vs 24.7 percent), neutropenia (46.0 percent vs 4.0 percent), nausea (45.1 percent vs 22.9 percent) and fatigue (39.9 percent vs 26.9 percent).
The most frequently reported grade 3 AEs in the Verzenio versus Faslodex -alone arms were neutropenia (23.6 percent vs 1.3 percent) and diarrhea (13.4 percent vs 0.4 percent). Grade 4 neutropenia occurred in 2.9 percent versus 0.4 percent of the Verzenio and Faslodex -alone groups, respectively. There were 3 deaths in the Verzenio arm linked to treatment-related AEs, compared with none in the control arm.
The MONARCH 1 trial included 132 patients with HR+/HER2- metastatic breast cancer who progressed during or after endocrine therapy and chemotherapy. The median age was 58 years (range, 36-89), 44.7 percent of patients had an ECOG performance status of 1, 90.2 percent had visceral disease, and 85.6 percent had at least two metastatic sites. Patients with CNS metastases were excluded from enrollment.
Patients had received a median of three (range, 1-8) prior lines of therapy—including a median of two lines of chemotherapy—for metastatic disease. Sixty-seven patients (50.8 percent) had received Faslodex in the metastatic setting. With chemotherapy, 68.9 percent (91 patients) of patients had received a taxane and 55.3 percent (73 patients) of patients had received capecitabine in the metastatic setting.
Verzenio was administered at 200 mg orally every 12 hours on a continuous schedule until progression or unacceptable toxicity. At the eight-month interim analysis, 35.6 percent of patients had received at least eight cycles of the CDK4/6 inhibitor.
Objective response rate (ORR) was the primary outcome measure. Secondary endpoints included duration of response, PFS, OS, clinical benefit rate, and safety.
The investigator-assessed, confirmed ORR was 19.7 percent (26 patients), which included all partial responses (PR). The rate of patients with stable disease (SD) at least six months was 22.7 percent, leading to a clinical benefit rate (complete response + PR + SD of six months or more) of 42.4 percent. The median time to response was 3.7 months and the median duration of response was 8.6 months. Thirty-four patients had progressive disease.
The most common non-laboratory, all-grade adverse events (AEs) were diarrhea (90.2 percent), fatigue (65.2 percent), nausea (64.4 percent), decreased appetite (45.5 percent) and abdominal pain (38.6 percent). The grade 3 rates of these events were 19.7 percent for diarrhea, 12.9 percent for fatigue, 4.5 percent for nausea, 3.0 percent for decreased appetite and 2.3 percent for abdominal pain.
Leukopenia (27.4 percent) and neutropenia (22.3 percent) were the most common laboratory AEs. The only grade 4 AE of any kind in the trial was neutropenia, which occurred in 4.6 percent of patients.
Serious AEs occurred in 24.2 percent (32 patients) of patients, with AEs leading to treatment discontinuation in 7.6 percent (10 patients) of patients. Dose reductions were required for 49.2 percent of patients (65 patients). The most common reason for dose reductions were diarrhea (20.5 percent) and neutropenia (10.6 percent). There were two patient deaths during treatment and one patient death within 30 days after study discontinuation.