Pembrolizumab Active in Heavily Pretreated Esophageal Tumors

Article

Treatment with the anti–PD-1 antibody pembrolizumab resulted in durable antitumor activity with manageable side effects in patients with heavily pretreated, PD-L1–positive advanced esophageal carcinoma, according to phase IB results of the KEYNOTE-028 study.

Treatment with the anti–programmed death-1 (PD-1) antibody pembrolizumab resulted in durable antitumor activity with manageable side effects in patients with heavily pretreated, PD-ligand 1 (PD-L1)-positive advanced esophageal carcinoma, according to phase IB results of the KEYNOTE-028 study published in the Journal of Clinical Oncology.

“Overall, tumor shrinkage from baseline in target lesions occurred in more than half the patients,” wrote Toshihiko Doi, MD, of National Cancer Center East, Japan, and colleagues.

KEYNOTE-028 was an international, multicenter, multi-cohort trial evaluating pembrolizumab in patients with 20 different types of PD-L1–positive advanced solid tumors. Patients were given pembrolizumab 10 mg/kg once every 2 weeks for up to 2 years or until progression, intolerable toxicity, or patient or investigator decision to discontinue. There were 83 patients with esophageal carcinoma and samples evaluable for PD-L1 expression; 37 had PD-L1 positive tumors and 23 were enrolled in the trial.

The median patient age was 65 years and most had squamous cell histology (78%). The majority of patients (87%) had two or more prior therapies for their disease.

At data cutoff, the median follow-up was 7 months. At that time, 39% of patients had treatment-related adverse events, the most common of which were decreased appetite, decreased lymphocyte count, generalized rash, and rash. No grade 4 or worse adverse events, or death, were attributed to pembrolizumab.

The overall response rate was 30%, with a median duration of response of 15 months. Responses occurred in patients with both adenocarcinoma and squamous cell histology. All of the responses were partial responses. Two additional patients had stable disease. The researchers found no pattern for responses related to prior chemotherapy regimen.

The median progression-free survival was 1.8 months and the 6-month and 12-month progression-free survival rates were 30% and 22%, respectively. The median overall survival was 7 months.

“Pembrolizumab demonstrated promising preliminary antitumor activity and a manageable safety profile in this heavily pretreated population of patients with PD-L1–positive advanced squamous cell carcinoma or adenocarcinoma of the esophagus enrolled in KEYNOTE-028,” the researchers wrote. “Evaluation of pembrolizumab for the treatment of esophageal carcinoma is ongoing.”

Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
Testing a patient’s genetics may influence decisions such as using longer courses of radiotherapy, says Rachit Kumar, MD.
Spatial transcriptomics and multiplex immunohistochemistry from samples may elucidate outcomes for patients who undergo surgical care for cancer.
Future work may focus on optimizing symptom management associated with percutaneous transesophageal gastrostomy placement in malignant bowel obstructions.
Post-operative length of stay ranged from 4 to 9 days for patients who underwent percutaneous transesophageal gastrostomy for malignant bowel obstructions.
Treatment with KRAS inhibitors may help mitigate a common driver of genetic alteration across a majority of pancreatic cancers.
Various methods of communication ensure that members from radiation oncology, pathology, and other departments are on the same page regarding treatment.
Updated results from the BREAKWATER study seemed to be most impactful to the CRC space, according to Michael J. Pishvaian, MD, PhD.
Related Content