Patterns and incidence of brain metastases in high-grade neuroendocrine carcinomas.

e14025 Background: High-grade neuroendocrine carcinomas (HGNEC) are aggressive malignancies with early dissemination. While small cell lung cancer (SCLC) is highly neurotropic, the incidence of brain metastases (BM) in large cell neuroendocrine carcinoma (LCNEC) and extrapulmonary NEC (EP-NEC) remains poorly characterized. We evaluated baseline and cumulative BM incidence and overall survival (OS) across HGNEC subtypes. Methods: Patients with HGNEC (SCLC, LCNEC, EP-NEC) treated at Roswell Park Comprehensive Cancer Center (2000–2024) were retrospectively reviewed. Baseline BM were intracranial lesions on imaging within 90 days of diagnosis; subsequent BM were new lesions >90 days post-diagnosis. Cumulative BM incidence was estimated using competing-risks methodology with death as the competing event. Multivariable Fine–Gray and Cox models assessed BM risk and OS. Results: Of 1665 patients (SCLC n=1215; EP-NEC n=366; LCNEC n=84), 270 (16.2%) had baseline BM. Baseline BM prevalence differed by histology (SCLC 19.5%, LCNEC 17.9%, EP-NEC 4.9%; p<0.001). Among 1394 patients without baseline BM, 24-month cumulative BM incidence was highest in SCLC (26.5%) versus LCNEC (10.1%) and EP-NEC (6.3%; p<0.001). SCLC had significantly higher subsequent BM risk versus EP-NEC (sHR 3.77, 95% CI 2.40–5.93; p<0.001). Median OS in BM-free patients was 15.8 months (SCLC), 20.2 months (LCNEC), and 13.9 months (EP-NEC; p=0.07); among patients with BM, median OS was 14.7, 14.1, and 10.3 months, respectively (p=0.054). Post-2018 diagnosis was associated with higher BM incidence (sHR 1.37, p=0.022) but improved OS (HR 0.79, p<0.001). Conclusions: In the largest single-institution HGNEC cohort reported to date, BM risk varies markedly by histology. SCLC demonstrates the highest baseline and cumulative BM incidence, followed by LCNEC, while EP-NEC shows the lowest CNS tropism. These findings support routine CNS surveillance for pulmonary HGNEC and a symptom-directed approach for EP-NEC. Histology SCLC (n=1215) EP-NEC (n=366) LCNEC (n=84) Baseline BM (%) 19.5 4.9 17.9 BM CI (%) 6/12/18/24 mo 3.6/17.7/23.7/26.5 2.0/4.6/6.0/6.3 1.4/7.2/10.1/10.1 OS, mo (BM-/BM+) 15.8/14.7 13.9/10.3 20.2/14.1 CI=cumulative incidence; OS=overall survival (months).

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Journal
Journal of Clinical Oncology
Published
2026-05-28
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.e14025
Primary Topic
Lung Cancer Research Studies
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article
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article

Patterns and incidence of brain metastases in high-grade neuroendocrine carcinomas.

Renuka Iyer, Prantesh Jain, Yongdong Ouyang, Reem Dergham et al.
Journal of Clinical Oncology
Lung Cancer Research Studies
article

Patterns and incidence of brain metastases in high-grade neuroendocrine carcinomas.

Renuka Iyer, Prantesh Jain, Yongdong Ouyang, Reem Dergham, Megan Wansart
article en

Abstract

e14025 Background: High-grade neuroendocrine carcinomas (HGNEC) are aggressive malignancies with early dissemination. While small cell lung cancer (SCLC) is highly neurotropic, the incidence of brain metastases (BM) in large cell neuroendocrine carcinoma (LCNEC) and extrapulmonary NEC (EP-NEC) remains poorly characterized. We evaluated baseline and cumulative BM incidence and overall survival (OS) across HGNEC subtypes. Methods: Patients with HGNEC (SCLC, LCNEC, EP-NEC) treated at Roswell Park Comprehensive Cancer Center (2000–2024) were retrospectively reviewed. Baseline BM were intracranial lesions on imaging within 90 days of diagnosis; subsequent BM were new lesions >90 days post-diagnosis. Cumulative BM incidence was estimated using competing-risks methodology with death as the competing event. Multivariable Fine–Gray and Cox models assessed BM risk and OS. Results: Of 1665 patients (SCLC n=1215; EP-NEC n=366; LCNEC n=84), 270 (16.2%) had baseline BM. Baseline BM prevalence differed by histology (SCLC 19.5%, LCNEC 17.9%, EP-NEC 4.9%; p<0.001). Among 1394 patients without baseline BM, 24-month cumulative BM incidence was highest in SCLC (26.5%) versus LCNEC (10.1%) and EP-NEC (6.3%; p<0.001). SCLC had significantly higher subsequent BM risk versus EP-NEC (sHR 3.77, 95% CI 2.40–5.93; p<0.001). Median OS in BM-free patients was 15.8 months (SCLC), 20.2 months (LCNEC), and 13.9 months (EP-NEC; p=0.07); among patients with BM, median OS was 14.7, 14.1, and 10.3 months, respectively (p=0.054). Post-2018 diagnosis was associated with higher BM incidence (sHR 1.37, p=0.022) but improved OS (HR 0.79, p<0.001). Conclusions: In the largest single-institution HGNEC cohort reported to date, BM risk varies markedly by histology. SCLC demonstrates the highest baseline and cumulative BM incidence, followed by LCNEC, while EP-NEC shows the lowest CNS tropism. These findings support routine CNS surveillance for pulmonary HGNEC and a symptom-directed approach for EP-NEC. Histology SCLC (n=1215) EP-NEC (n=366) LCNEC (n=84) Baseline BM (%) 19.5 4.9 17.9 BM CI (%) 6/12/18/24 mo 3.6/17.7/23.7/26.5 2.0/4.6/6.0/6.3 1.4/7.2/10.1/10.1 OS, mo (BM-/BM+) 15.8/14.7 13.9/10.3 20.2/14.1 CI=cumulative incidence; OS=overall survival (months).

Journal of Clinical OncologyVol. 44(16_suppl)
Roswell Park Comprehensive Cancer Center (US)
Good health and well-being
Openalex Percentile: Top 7%
Lung Cancer Research Studies
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