Pembrolizumab and Peptide Receptor Radionuclide Therapy for Patients with Metastatic Well-Differentiated Neuroendocrine Tumors

PURPOSE: Objective responses to peptide receptor radionuclide therapy (PRRT) for pre-treated patients with well-differentiated neuroendocrine tumors (WD-NET) and Ki-67 index >10% may not be durable. Response rate to single agent immune checkpoint inhibitors for patients with WD-NET is low. Targeted radiation using PRRT may potentiate anti-tumor immune response. This study evaluated safety and efficacy of the combination of PRRT and the PD-1 inhibitor pembrolizumab in high-risk WD-NET. PATIENTS AND METHODS: In a single arm prospective pilot study, adult patients with WHO grade 2 or 3 well-differentiated (Ki-67 index >10%) somatostatin receptor avid metastatic NET of any primary site received concurrent pembrolizumab and 177Lu-DOTATATE PRRT. Primary endpoint was objective response rate (ORR) by RECIST v.1.1. Secondary endpoints were progression free survival (PFS), overall survival, and safety. RESULTS: A total of 26 patients were enrolled, including 20 patients with grade 3 NET. Median PFS was 13.3 months (range 2.1-33.4 months). ORR was 35%. Median overall survival was 24.1 months (range 4.4 to 52.3 months). Severe adverse events (SAE) occurred in 14 (54%) patients. The most common immune-related AEs were grade 1 or 2 hepatitis (n=7), grade 2 hypothyroidism (n=5), and diabetes mellitus (n=4). Clinical responses were associated with higher baseline frequencies of proliferating CD8+ T cells and lower frequencies of CD14+ myeloid-derived suppressor cells in the peripheral blood. CONCLUSIONS: Added benefit of CPI to PRRT for patients with high risk WD-NET remains unclear. SAE rate was higher than expected for PRRT alone.

Authors

Institutions

Publication Details

Journal
Clinical Cancer Research
Published
2026-09-28
DOI
https://doi.org/10.1158/1078-0432.ccr-26-1617
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Pembrolizumab and Peptide Receptor Radionuclide Therapy for Patients with Metastatic Well-Differentiated Neuroendocrine Tumors

Bridget P. Keenan, Alexander Cheung, Emily K. Bergsland, Ciara Benson et al.
Clinical Cancer Research
Neuroendocrine Tumor Research Advances
article

Pembrolizumab and Peptide Receptor Radionuclide Therapy for Patients with Metastatic Well-Differentiated Neuroendocrine Tumors

Bridget P. Keenan, Alexander Cheung, Emily K. Bergsland, Ciara Benson, David Yoonsuk Oh, Nicholas A. Fidelman, Thomas A. Hope, Lawrence H. Fong, Arun K. Chumber, Li Zhang, Kira Chan, Kiersten Tucker
article en

Abstract

PURPOSE: Objective responses to peptide receptor radionuclide therapy (PRRT) for pre-treated patients with well-differentiated neuroendocrine tumors (WD-NET) and Ki-67 index >10% may not be durable. Response rate to single agent immune checkpoint inhibitors for patients with WD-NET is low. Targeted radiation using PRRT may potentiate anti-tumor immune response. This study evaluated safety and efficacy of the combination of PRRT and the PD-1 inhibitor pembrolizumab in high-risk WD-NET. PATIENTS AND METHODS: In a single arm prospective pilot study, adult patients with WHO grade 2 or 3 well-differentiated (Ki-67 index >10%) somatostatin receptor avid metastatic NET of any primary site received concurrent pembrolizumab and 177Lu-DOTATATE PRRT. Primary endpoint was objective response rate (ORR) by RECIST v.1.1. Secondary endpoints were progression free survival (PFS), overall survival, and safety. RESULTS: A total of 26 patients were enrolled, including 20 patients with grade 3 NET. Median PFS was 13.3 months (range 2.1-33.4 months). ORR was 35%. Median overall survival was 24.1 months (range 4.4 to 52.3 months). Severe adverse events (SAE) occurred in 14 (54%) patients. The most common immune-related AEs were grade 1 or 2 hepatitis (n=7), grade 2 hypothyroidism (n=5), and diabetes mellitus (n=4). Clinical responses were associated with higher baseline frequencies of proliferating CD8+ T cells and lower frequencies of CD14+ myeloid-derived suppressor cells in the peripheral blood. CONCLUSIONS: Added benefit of CPI to PRRT for patients with high risk WD-NET remains unclear. SAE rate was higher than expected for PRRT alone.

Clinical Cancer Research
Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA), University of California, San Francisco (US), Fred Hutch Cancer Center (US), University of California San Francisco Medical Center (US), The Ohio State University (US), University of San Francisco (US), University of St. Francis (US)
Openalex Percentile: Top 11%
Neuroendocrine Tumor Research Advances
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.