A Phase I safety and pharmacokinetic (PK) study of recombinant Apo2L/TRAIL, an apoptosis-inducing protein in patients with advanced cancer.
Reviewer: John P. Plastaras, MD, PhD
Abramson Cancer Center of the University of Pennsylvania
Last Modified: June 3, 2006
Presenter: Roy S. Herbst Presenter's Affiliation: M. D. Anderson Cancer Center, Houston, TX Type of Session: Scientific
Death receptors, such as TNF-alpha receptor, Fas, and TRAIL-R (TNF-alpha Related Apoptosis Inducing Ligand Receptor)-1 and –2, can stimulate the extrinsic apoptotic pathway in tumor cells when activated by their cognate ligands
Stimulation of TNF-alpha receptor and Fas has been associated with unacceptable systemic toxicities, limiting the clinical utility of targeting these pathways. In contrast, pre-clinical data has shown that stimulation of the TRAIL receptor can selectively kill tumor cells without systemic toxicity
The ligand Apo2L/TRAIL can activate both of the human TRAIL receptors: TRAIL-R1 (DR4) and TRAIL-R2 (DR5) - Apo2L/TRAIL induces apoptosis in human tumor cell lines in vitro and in xenograft models. Its efficacy is p53-independent.
A His-tagged preparation of TRAIL was toxic to primary human hepatocytes in culture. In contrast, the preparation of native TRAIL being developed by Genentech and Amgen has no foreign sequences and is not toxic to primary human hepatocytes, nor is it toxic in murine or primate models.
This is the first report on the safely of Apo2L/TRAIL administered to humans.
Materials and Methods
Phase I study design:
Open label study conducted at five centers
58 patients with advanced solid tumors or NHL; 586 doses administered
Dose escalation: 0.5, 1.5, 4, 8, and 15 mg/kg i.v. administered daily for 5 days every 3 weeks
Given concerns surrounding potential hepatotoxicity, patients without liver metastasis were treated before patients with liver metastasis in a staggered manner
Toxicity, pharmacokinetics, immunogenicity and best responses were assessed
Median age: 59. Heavily pre-treated (median prior regimens = 4)
No dose limiting toxicities were observed in any of the cohorts.
Most of the adverse events were Grade 1/2 fatigue, nausea, and anemia
There were 2 each of Grade 3 hyperglycemia, pneumonia, and AST elevation.
All patients with liver toxicities had progressive disease
Two patients with sarcoma had adverse events related to tumor necrosis
Of the assessable patients, 53% had stable disease, 41% had progressive disease.
One patient with synovial chondrosarcoma treated with 8 mg/kg had a confirmed, objective partial response (70% by RECIST criteria)
Dose dependent and linear, which did not differ depending on presence of liver metastasis
half-life was 0.6 hr
No antibodies against Apo2L/TRAIL were detected.
Apo2L/TRAIL is safe and well tolerated up to 15 mg/kg. The 8 mg/kg cohort is being expanded for additional safety data.
Combination with other chemotherapeutic agents is warranted.
There was considerable trepidation regarding liver toxicity that was engendered by in vitro results using a His-TRAIL preparation. Therefore, it is significant that there were no dose limiting toxicities in this Phase I trial, even in patients with liver metastasis.
The partial response seen in one patient with chondrosarcoma was promising, however, like the agonistic antibodies, the majority of responses were stable disease
Unlike the agonistic antibodies, Apo2L/TRAIL targets both TRAIL-R1 and TRAIL-R2, which may broaden its efficacy. However, the short half-life requires an inconvenient dosing regimen (i.v. injections every day for 5 days) to get the predicted AUC required for activity.
There is marked heterogeneity in TRAIL sensitivity in human tumor cell lines, and the mechanisms of resistance are protean. Future studies should focus on optimal combination therapies with TRAIL, as its activity as a single-agent will likely be underwhelming.
Jan 26, 2012 - An A20 ligase mediates ubiquitination to inhibit tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis in glioblastoma cells, according to an experimental study published online Jan. 24 in Cancer Discovery.