Immunotherapy May Be a Treatment Option for Mesothelioma

Patients with mesothelioma may be getting a new second-line treatment, thanks to results from a recent immunotherapy trial.
BY Allie Casey
PUBLISHED April 02, 2017
For patients with malignant pleural mesothelioma – which makes up about 90 percent of malignant mesothelioma cases – chemotherapy is the only frontline approved therapy, with no options for second-line treatment.
 
However, this may change soon, as findings from a group of patients in the KEYNOTE-028 study suggest that the PD-L1 checkpoint inhibitor Keytruda (pembrolizumab) may be effective in treating this disease.
 
Researchers note that this is first study to present positive findings from a checkpoint inhibitor immunotherapy drug for the treatment of malignant pleural mesothelioma. The disease is primarily caused by the inhalation of asbestos, a fiber commonly found in some forms of insulation, vinyl floor tiles, and other material. Tumors form in the pleura, a thin membrane of cells that line the lungs and chest wall. Most patients survive less than one year. This poor prognosis is partially due to the fact that most patients are not diagnosed until they are already at a late stage of the disease.
 
KEYNOTE-028 is an ongoing phase 1b trial (NCT02054806) involving 13 different research sites in six different countries examining the effect of Keytruda on patients with advanced malignancies, including malignant pleural mesothelioma. This study evaluated a subset of 25 patients with this disease and an ECOG performance status of 0 or 1 who had either already been treated with chemotherapy or were unable to receive chemotherapy. None of the patients had been treated with a checkpoint inhibitor prior to the study. Investigators used immunohistochemistry to determine PD-L1 positivity, defined as expression on 1 percent or more of tumor cells  
 
The first patients were enrolled two years ago and received a dose of Keytruda (10 mg/kg) every two weeks for up to two years until progression or intolerable toxicity. Median duration of therapy was 5.1 months. Fourteen patients experienced a reduction in tumor size. Median progression-free survival was 5.4 months and median overall survival was 18 months. Fourteen patients died during the study, nine due to disease progression. Median duration of response was 12 months.
 
At the time of data cutoff June 20, 2016, 21 patients had discontinued treatment, two remained on the drug and two had completed the maximum 24 months of treatment set by the investigators.
 
“Most patients who receive a second-line therapy have a life expectancy of about six or seven months, so to have four patients still ongoing at two years is very encouraging,” noted Evan Alley, M.D., Ph.D., the study’s lead author and chief of hematology and medical oncology at Penn Presbyterian Hospital.
 
Sixteen of the 25 patients on this arm of the study experienced an adverse event (AE). The most common AEs in the mesothelioma cohort were grade 1/2 fatigue and nausea (reported in six patients each) and grade 1/2 arthralgia (five patients).  
 
Overall, however, “one great sign in this study is that none of the patients had to stop treatment because of side-effects,” Alley continued, although three patients had a dose interruption due to an immune-related AE: “Some had temporary stoppages, but they were able to continue. The drug appears to be well-tolerated.”
 
Study authors concluded that, “Pembrolizumab appears to elicit significant clinical activity with durable responses and a manageable safety and toxicity profile in patients with PD-L1-positive malignant pleural mesothelioma, with tolerable safety, an indication of clinical activity, and substantial duration of response.”
 
Currently multiple studies are under way to confirm these findings. There are already plans for future trials testing the combination of Keytruda with other treatments, two of which will be conducted at Penn. These studies are expected to launch later in 2017. “This study provides evidence that some patients can have long-term disease control with this drug, which we haven’t seen before,” Alley said. “We need to better understand what we can do next to make immunotherapy more effective for more patients.”
 
 
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