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Antitumor activity of the combination of axitinib (Inlyta) and pembrolizumab (Keytruda) is superior to that expected from axitinib or PD-1/PD-L1 pathway inhibitor monotherapy in treatment-naïve patients with advanced renal cell carcinoma.
Michael Atkins, MD
Antitumor activity of the combination of axitinib (Inlyta) and pembrolizumab (Keytruda) is superior to that expected from axitinib or PD-1/PD-L1 pathway inhibitor monotherapy in treatment-naïve patients with advanced renal cell carcinoma, according to results from an open-label phase Ib single-arm clinical trial.
In addition, fewer liver function test abnormalities and less fatigue were reported compared with other combinations of VEGF inhibitors and PD-1 checkpoint inhibitors, lead investigator Michael B. Atkins, MD, said at the 2018 Genitourinary Cancers Symposium.
“The regimen was highly active,” he said, with 38 of 52 patients (73.1%) enrolled in the dose-finding and dose-expansion phases of the study having objective responses with the axitinib/pembrolizumab combination. Best overall response was a complete response in 4 patients (7.7%), partial response in 34 (65.4%), and stable disease in 8 (15.4%). The median progression-free survival was 20.9 months (95% CI, 15.4 to not evaluable). Median overall survival was not reached at a minimum follow-up of 17.6 months.
Prior studies in which VEGF inhibitors were combined with PD-1 checkpoint inhibitors were plagued by excess toxicity. Many of these toxicities were related to off-target effects of multitargeted tyrosine kinase inhibitors. The possibility that a more selective VEGF inhibitor would improve tolerability when combined with a PD-1 inhibitor while offering synergistic antitumor activity was the basis for the phase Ib study that Atkins reported at the symposium.
In the study, 11 treatment-naïve patients were enrolled in a dose-finding phase to estimate the maximum-tolerated dose and 41 in a dose-expansion phase. Axitinib at 5 mg was administered orally twice daily and pembrolizumab at 2 mg/kg was given intravenously every 3 weeks.
Tumors were assessed using RECIST v1.1 at baseline, week 12, and then every 6 weeks. The primary endpoint was dose-limiting toxicity during the first 2 cycles (6 weeks). “Per protocol, according to the investigators’ judgment, patients with evidence of disease progression experiencing what was thought to be clinical benefit were eligible for continued treatment,” said Atkins, deputy director, Georgetown-Lombardi Comprehensive Cancer Center.
To be included in the study, patients had to have treatment-naïve clear cell kidney cancer, prior nephrectomy, at least 1 measureable lesion by RECIST v1.1, an ECOG performance status of 0 or 1, and controlled hypertension.
Of the 11 patients treated in the dose-finding phase, 3 dose-limiting toxicities were reported. One patient had a transient ischemic attack. “Axitinib was held, she recovered from the event, axitinib was restarted at a lower dose, and she remains on therapy with a response almost 3 years later,” Atkins said. Two others could not complete at least 75% of the planned axitinib dose, 1 due to a grade 2/3 headache and another due to grade 3 headache, fatigue, asthenia, and dehydration. The maximum-tolerated dose, therefore, was estimated to be axitinib at 5 mg twice daily and pembrolizumab at 2 mg/kg every 3 weeks.
The entire cohort of 52 patients had a median age of 63 years (range, 28-75). Forty-six percent had a favorable International Metastatic Renal Cell Carcinoma Database risk score, although 26.9% of patients had Fuhrman grade 4 tumors. The median time from nephrectomy and initiation of therapy was 20.3 months.
As of the data cutoff on March 31, 2017, there were 25 patients on treatment, 22 were receiving the combination and 3 were receiving pembrolizumab only. Eight patients with confirmed disease progression were still receiving treatment for continued clinical benefit. Of the 27 patients who discontinued both study treatments, 10 did so for adverse events, 9 because of disease progression, 5 because of mixed disease progression and adverse events, and 3 for other reasons.
The median duration of axitinib/pembrolizumab treatment was 14.5 months. Some 61.5% of patients had their axitinib dose reduced to <5 mg twice weekly for at least 2 consecutive doses. One patient had an axitinib dose increase to 7 mg twice daily. The median dose of axitinib was 8.8 mg/day and the median dose of pembrolizumab was 2.0 mg/kg per cycle.
More than 90% of patients had tumor shrinkage. “Except in rare cases, continued treatment beyond disease progression was characterized more by stabilization or slow, continued progression rather than regression,” said Atkins.
The median time to response was 2.8 months (range 0.7-15.2 months) and the median duration of tumor response was 18.6 months. Nineteen of the 38 responders were continuing to respond at the time of data cutoff, including 17 patients who were still on therapy. Ten patients who discontinued both agents because of toxicity were censored even though their disease had not progressed, and 5 were still responding to treatment, Atkins noted.
“There were only 6 deaths total, 4 related to the disease under study and 2 for unrelated reasons,” he said.
About two-thirds (65.4%) had grade ≥3 toxicities. “Most of these were axitinib-related, with 23% having hypertension,” Atkins said. The other most common grade ≥3 adverse events were diarrhea (9.6%), fatigue (9.6%), and an increase in the level of ALT (7.7%). The most common immune-related grade ≥3 adverse events were diarrhea (7.7%), an increase in ALT (3.8%), an increase in the level of AST (3.8%), and fatigue (3.8%).
“Whether the combination works better than a sequence of a VEGF pathway inhibitor followed by an anti—PD-1 therapy awaits the completion of the phase III KEYNOTE-426 trial comparing axitinib/pembrolizumab with sunitinib,” said Atkins.
Atkins MB, Plimack ER, Puzanov I, et al. Safety and efficacy of axitinib (axi) in combination with pembrolizumab (pembro) in patients (pts) with advanced renal cell cancer (aRCC). Presented at: 2018 Genitourinary Cancers Symposium; February 8-10, 2018; San Francisco, Calif. Abstract 579.