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Phase II trial of pembrolizumab in patients with platinum refractory germ-cell tumors: a Hoosier Cancer Research
N Adra1, L H Einhorn1, S K Althouse2
1Melvin & Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, USA.
Background:
Despite remarkable results with salvage standard-dose or high-dose chemotherapy ∼15% of patients with relapsed germ-cell tumors (GCT) are incurable. Immune checkpoint inhibitors have produced significant remission in multiple tumor types. We report the first study of immunotherapy in patients with GCT.
Patients And Methods:
Single arm phase II trial investigating pembrolizumab 200 mg i.v. Q3weeks until disease progression in patients with relapsed GCT and no curable options. Patients age ≥18 with GCT who progressed after first-line cisplatin-based chemotherapy and after at least one salvage regimen (high-dose or standard-dose chemotherapy) were eligible. Centrally assessed programmed death-ligand 1 (PD-L1) on tumor and infiltrating immune cells was scored. Primary end point was overall response rate using immune-related response criteria. Simon two-stage design with type I error 20% and power 80% was utilized.
Results:
Twelve male patients were enrolled. Median age was 38 years. All patients had nonseminoma. Primary site was testis (11) or mediastinum (1). Median AFP 615 (range 1-32, 760) and hCG 4 (range 0.6-37, 096). Six patients had late relapse (>2 years). Median number of previous chemotherapy regimens was 3. Six patients received prior high-dose chemotherapy. Two patients had positive PD-L1 staining (H-score 90 and 170). Median number of pembrolizumab doses was 2 (range 1-8). There were six grade 3 adverse events. No immune-related adverse events were reported. No partial or complete responses were observed. Two patients achieved radiographic stable disease for 28 and 19 weeks, respectively; both had continued rising AFP level despite radiographic stability and had negative PD-L1 staining.
Conclusion:
This is the first reported trial evaluating immune checkpoint inhibitors in GCT. Pembrolizumab is well tolerated but does not appear to have clinically meaningful single-agent activity in refractory GCT.
Clinical Trial Information:
NCT02499952.
Insights
This study evaluated pembrolizumab for relapsed germ-cell tumors (GCT) in patients with no other options. The immunotherapy was well-tolerated but showed no significant clinical activity in refractory GCT.
Area of Science:
- Oncology
- Immunotherapy
- Clinical Trials
Background:
- Relapsed germ-cell tumors (GCT) present a challenge, with approximately 15% of patients remaining incurable despite salvage chemotherapy.
- Immune checkpoint inhibitors (ICIs) have shown promise in various cancers, prompting investigation in GCT.
Purpose of the Study:
- To evaluate the efficacy and safety of pembrolizumab, an immune checkpoint inhibitor, as a single-agent therapy in patients with relapsed GCT who have exhausted conventional treatment options.
- To determine the overall response rate (ORR) using immune-related response criteria in this patient population.
Main Methods:
- A single-arm, phase II trial enrolled 12 male patients with relapsed GCT who progressed after first-line chemotherapy and at least one salvage regimen.
- Patients received pembrolizumab 200 mg intravenously every 3 weeks until disease progression. Programmed death-ligand 1 (PD-L1) expression was assessed.
- The primary endpoint was the overall response rate, assessed using immune-related response criteria. A Simon two-stage design was employed.
Main Results:
- Pembrolizumab was administered for a median of 2 doses. Six patients experienced grade 3 adverse events, but no immune-related adverse events were reported.
- No partial or complete responses were observed. Two patients achieved radiographic stable disease for 28 and 19 weeks, respectively, despite rising AFP levels and negative PD-L1 staining.
Conclusions:
- This is the first study to report on the use of immune checkpoint inhibitors in germ-cell tumors.
- Pembrolizumab demonstrated good tolerability in patients with refractory GCT but did not show clinically meaningful single-agent activity.
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