Outcomes of Chemoimmunotherapy in Metastatic Pancreatic Neuroendocrine Carcinoma: A Single-Center Clinicopathologic Study

BACKGROUND: Pancreatic neuroendocrine carcinomas (PanNECs) are a rare, aggressive subtype of pancreatic neuroendocrine neoplasms. Based upon similarities to small cell lung cancer (SCLC), advanced PanNECs are commonly treated with platinum and etoposide chemotherapy; however, outcomes remain poor. Although first-line chemoimmunotherapy has improved survival in SCLC, its role in PanNEC is not well defined. METHODS: We report on a retrospective cohort of 13 patients with metastatic PanNEC treated at Memorial Sloan Kettering with either first-line combined chemoimmunotherapy or first-line chemotherapy alone. RESULTS: In the first-line metastatic setting, patients who received chemoimmunotherapy (N = 5) demonstrated longer median progression-free survival (17.0 months vs. 2.8 months, P = 0.002) and overall survival (31.0 months vs. 16.0 months, P = 0.031) compared with those who received chemotherapy alone (N = 8). In the second line or later setting, five patients received immunotherapy-containing regimens with a median progression free survival of only 3.0 months (95% confidence interval 1.4 months, Not Reached). Radiologic responses observed in patients receiving chemoimmunotherapy in the first-line metastatic setting were 2 complete responses and 3 partial responses. Germline variants included one patient with a BRCA2 mutation, one patient with co-existing BRCA2 and ATM mutations, and one patient with a MUTYH mutation. Exploratory genomic analyses showed common mutations in TP53, RB1, and KRAS, low tumor mutational burden, and microsatellite stability. Exploratory multiplex immunofluorescence demonstrated heterogenous immune cell infiltrates without a consistent biomarker pattern associated with response. CONCLUSION: In this single-center cohort, early incorporation of chemoimmunotherapy in PanNEC was associated with improved survival. These findings are hypothesis-generating and support prospective, multicenter evaluation of first-line chemoimmunotherapy strategies in PanNEC (SWOG S2012, NCT05058651) [1].

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Journal
The Oncologist
Published
2026-10-27
DOI
https://doi.org/10.1093/oncolo/oyag429
Primary Topic
Neuroendocrine Tumor Research Advances
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article
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article

Outcomes of Chemoimmunotherapy in Metastatic Pancreatic Neuroendocrine Carcinoma: A Single-Center Clinicopathologic Study

Rohit Thummalapalli, Danny N. Khalil, Wungki Park, Joanne F. Chou et al.
The Oncologist
Neuroendocrine Tumor Research Advances
article

Outcomes of Chemoimmunotherapy in Metastatic Pancreatic Neuroendocrine Carcinoma: A Single-Center Clinicopathologic Study

Rohit Thummalapalli, Danny N. Khalil, Wungki Park, Joanne F. Chou, Marinela Capanu, Marc Hilmi, Catherine Anne O'Connor, Nitya Prabhakar Raj, Daniel M. Muldoon, Geoffrey Yuyat Ku, Maria Perry, Eileen Mary O'Reilly, Zoe Goldberg, Olca Baştürk, Chaitanya Bandlamudi, Tae-Hyung Kim, Drew Moss, Nuray Tezcan, Christine Iacobuzio, James Harding, Ziv Etay
article en

Abstract

BACKGROUND: Pancreatic neuroendocrine carcinomas (PanNECs) are a rare, aggressive subtype of pancreatic neuroendocrine neoplasms. Based upon similarities to small cell lung cancer (SCLC), advanced PanNECs are commonly treated with platinum and etoposide chemotherapy; however, outcomes remain poor. Although first-line chemoimmunotherapy has improved survival in SCLC, its role in PanNEC is not well defined. METHODS: We report on a retrospective cohort of 13 patients with metastatic PanNEC treated at Memorial Sloan Kettering with either first-line combined chemoimmunotherapy or first-line chemotherapy alone. RESULTS: In the first-line metastatic setting, patients who received chemoimmunotherapy (N = 5) demonstrated longer median progression-free survival (17.0 months vs. 2.8 months, P = 0.002) and overall survival (31.0 months vs. 16.0 months, P = 0.031) compared with those who received chemotherapy alone (N = 8). In the second line or later setting, five patients received immunotherapy-containing regimens with a median progression free survival of only 3.0 months (95% confidence interval 1.4 months, Not Reached). Radiologic responses observed in patients receiving chemoimmunotherapy in the first-line metastatic setting were 2 complete responses and 3 partial responses. Germline variants included one patient with a BRCA2 mutation, one patient with co-existing BRCA2 and ATM mutations, and one patient with a MUTYH mutation. Exploratory genomic analyses showed common mutations in TP53, RB1, and KRAS, low tumor mutational burden, and microsatellite stability. Exploratory multiplex immunofluorescence demonstrated heterogenous immune cell infiltrates without a consistent biomarker pattern associated with response. CONCLUSION: In this single-center cohort, early incorporation of chemoimmunotherapy in PanNEC was associated with improved survival. These findings are hypothesis-generating and support prospective, multicenter evaluation of first-line chemoimmunotherapy strategies in PanNEC (SWOG S2012, NCT05058651) [1].

The Oncologist
Memorial Sloan Kettering Cancer Center (US), Harvard University (US), Parker Institute for Cancer Immunotherapy (US), Weill Cornell Medicine (US), Institut Curie (FR)
Openalex Percentile: Top 11%
Neuroendocrine Tumor Research Advances
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