Immune Checkpoint Inhibitors Hold Promise In Glioblastoma

Dale Chenoweth
Published: Friday, Nov 20, 2015

 Michael Lim, MD

Michael Lim, MD

The newly emerging class of immune checkpoint blockade drugs has produced impressive benefits for patients in several solid tumor types and there are reasons to suggest this strategy may be successful against central nervous system tumors as well, including glioblastoma, said Michael Lim, MD, in a presentation at the 2015 Society for Neuro-Oncology Annual Meeting.

“Although it’s relatively new, this approach is changing the paradigm of cancer therapy,” said Lim, director of Brain Tumor Immunotherapy and associate professor of Neurosurgery at Johns Hopkins University School of Medicine in Baltimore.

The success of monoclonal antibodies targeting immune checkpoints in melanoma and non–small cell lung cancer (NSCLC) has attracted the interest of researchers seeking new therapies against glioblastoma, Lim indicated. The rationale for employing this strategy in glial tumors also has been established in preclinical studies.

Ipilimumab (Yervoy), which inhibits CTLA-4, launched the checkpoint field in 2011 when the FDA approved the drug for patients with unresectable or metastatic melanoma. Since September 2014, the FDA has approved the PD-1 inhibitors nivolumab (Opdivo) and pembrolizumab (Keytruda) in melanoma and NSCLC, and additional agents that target the PD-1 ligand, PD-L1, are advancing in clinical development. Nivolumab also is approved in combination with ipilimumab for patients with BRAF V600 wild-type metastatic melanoma.

In an article submitted as part of the conference, Lim and colleague William T. Curry, MD, a neurosurgeon at Massachusetts General Hospital, noted three clinical studies currently under way that are evaluating checkpoint inhibitors in patients with glioblastoma1:

  • Nivolumab—The CheckMate 143 study is comparing nivolumab alone (3 mg/kg) versus bevacizumab alone (10 mg/kg) in patients with recurrent glioblastoma.1,2 Preliminary results from one cohort presented at the 2015 ASCO Annual Meeting demonstrated that nivolumab monotherapy was well tolerated without treatment-related grade 3/4 adverse events.The trial also was designed to test the safety of nivolumab alone versus the combination of nivolumab and ipilimumab, but 4 of 10 patients discontinued the combination because of toxicities.1  The trial is now proceeding to phase III as a comparison of nivolumab monotherapy with bevacizumab.The estimated completion date for collecting data on the primary outcome measures of safety and overall survival is June 2017.2 An estimated 440 patients are expected to enroil.
  • Pembrolizumab—Researchers at Dana-Farber Cancer Institute have launched a single-center phase II study randomizing participants to pembrolizumab alone or in combination with bevacizumab. The study, which seeks to enroll about 80 participants with grade 4 malignant glioma at first or second relapse, has a primary endpoint of 6-month progression-free survival and a primary completion date of February 2017.3
  • Durvalumab—The PD-L1 inhibitor, formerly known as MEDI4736, is being evaluated in a 3-cohort, phase II trial. The cohorts consist of patients who will receive durvalumab with these regimens: (a)  in combination with standard radiotherapy in patients with newly diagnosed unmethylated MGMT glioblastoma; (b) as monotherapy in bevacizumab-naïve patients with recurrent disease; (c) in combination with continued bevacizumab in bevacizumab-refractory patients with recurrent glioblastoma.4  The trial, which aims to enroll approximately 100 participants, has a primary completion date of April 2017.

Many Ways to Explore Checkpoints

A variety of strategies are being employed as researchers explore the concept of immune checkpoint modulation in glioblastoma, Lim indicated.

In addition to the PD-1 and CTLA-4 checkpoints, preclinical murine studies against gliomas have delved into agents that target the co-inhibitory Tim3 checkpoint and the co-stimulatory CD137 checkpoint.  In each study, the antitumor effect was mediated by T-cell populations: either CD4-positive T cells, CD8-positive T cells, or both. In both studies, the improved survival was again seen when the mice were challenged anew with the same tumor.

Because of the marked increase in overall survival seen with combined checkpoint inhibitors in some tumor types, combinating such agents is becoming one of the exciting new directions in which the field is moving, Lim noted. Another strategy being explored is the combination of immune checkpoint inhibitors with other immunotherapies, such as other agents that stimulate immune responses, IDO pathway inhibitors, and viruses.  




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