TY - JOUR
T1 - Real-world risk of brain metastases in stage III non-small cell lung cancer in the era of PET and MRI staging
AU - Alhusaini, Saud
AU - Lanman, Tyler A.
AU - Ko, Ryan B.
AU - Therkelsen, Kate E.
AU - Eyben, Rie Von
AU - Diehn, Maximilian
AU - Soltys, Scott G.
AU - Pollom, Erqi L.
AU - Chin, Alexander
AU - Vitzthum, Lucas
AU - Wakelee, Heather A.
AU - Padda, Sukhmani K.
AU - Ramchandran, Kavitha
AU - Loo, Billy W.
AU - Neal, Joel W.
AU - Nagpal, Seema
N1 - Publisher Copyright:
Copyright © 2023 Alhusaini, Lanman, Ko, Therkelsen, Eyben, Diehn, Soltys, Pollom, Chin, Vitzthum, Wakelee, Padda, Ramchandran, Loo, Neal and Nagpal.
PY - 2023
Y1 - 2023
N2 - OBJECTIVE: The 2-year incidence of brain metastases (BrMs) in stage III non-small lung cell cancer (NSCLC) has been estimated to be around 30%. However, recent clinical trials have demonstrated considerably lower BrMs rates in this patient population. In this study, we aimed to review the real-world incidence, surveillance, and treatment patterns of BrMs in stage III NSCLC.MATERIALS AND METHODS: Using a retrospective single-center study design, we identified patients with stage III NSCLC who received radiation with curative intent over a 10-year period. Outcome variables included BrMs incidence, overall survival (OS), and survival from date of BrMs. Additionally, we assessed patterns of BrMs surveillance in stage III NSCLC and treatment.RESULTS: We identified a total of 279 stage III NSCLC patients, of which 160 with adequate records were included in the final analyses [adenocarcinoma (n = 96), squamous cell carcinoma (n = 53), other histology subtype (n = 11)]. The median OS for the entire cohort was 41 months (95% CI, 28-53), while the median time from BrMs to death was 19 months (95% CI, 9-21). Twenty-three patients (14.4%) received planned surveillance brain MRIs at 6, 12, and 24 months after completion of treatment. The remaining 137 patients (85.6%) received brain MRIs at systemic recurrence (restaging) or when neurologically symptomatic. A total of 37 patients (23%) developed BrMs, with a 2-year cumulative BrMs incidence of 17% (95% CI, 11-23). A higher incidence of BrMs was identified in patients with adenocarcinoma relative to those with squamous cell carcinoma (
p < 0.01). Similarly, a higher 2-year BrMs incidence was observed in patients who received planned surveillance brain MRI relative to those who did not, although statistical significance was not reached. Stereotactic radiosurgery (SRS) treated 29 of BrMs patients (78.4%) and was preferred over WBRT, which treated only 3 patients (8.1%).
CONCLUSIONS: At our center, BrMs incidence in stage III NSCLC patients was lower than historically reported but notably higher than the incidence described in recent clinical trials. Routine BrMs surveillance potentially allows earlier detection of asymptomatic BrMs. However, asymptomatic BrMs were mostly detected on restaging MRI at the time of recurrence.
AB - OBJECTIVE: The 2-year incidence of brain metastases (BrMs) in stage III non-small lung cell cancer (NSCLC) has been estimated to be around 30%. However, recent clinical trials have demonstrated considerably lower BrMs rates in this patient population. In this study, we aimed to review the real-world incidence, surveillance, and treatment patterns of BrMs in stage III NSCLC.MATERIALS AND METHODS: Using a retrospective single-center study design, we identified patients with stage III NSCLC who received radiation with curative intent over a 10-year period. Outcome variables included BrMs incidence, overall survival (OS), and survival from date of BrMs. Additionally, we assessed patterns of BrMs surveillance in stage III NSCLC and treatment.RESULTS: We identified a total of 279 stage III NSCLC patients, of which 160 with adequate records were included in the final analyses [adenocarcinoma (n = 96), squamous cell carcinoma (n = 53), other histology subtype (n = 11)]. The median OS for the entire cohort was 41 months (95% CI, 28-53), while the median time from BrMs to death was 19 months (95% CI, 9-21). Twenty-three patients (14.4%) received planned surveillance brain MRIs at 6, 12, and 24 months after completion of treatment. The remaining 137 patients (85.6%) received brain MRIs at systemic recurrence (restaging) or when neurologically symptomatic. A total of 37 patients (23%) developed BrMs, with a 2-year cumulative BrMs incidence of 17% (95% CI, 11-23). A higher incidence of BrMs was identified in patients with adenocarcinoma relative to those with squamous cell carcinoma (
p < 0.01). Similarly, a higher 2-year BrMs incidence was observed in patients who received planned surveillance brain MRI relative to those who did not, although statistical significance was not reached. Stereotactic radiosurgery (SRS) treated 29 of BrMs patients (78.4%) and was preferred over WBRT, which treated only 3 patients (8.1%).
CONCLUSIONS: At our center, BrMs incidence in stage III NSCLC patients was lower than historically reported but notably higher than the incidence described in recent clinical trials. Routine BrMs surveillance potentially allows earlier detection of asymptomatic BrMs. However, asymptomatic BrMs were mostly detected on restaging MRI at the time of recurrence.
KW - MRI brain
KW - brain metastases
KW - incidence
KW - non-small cell lung cancer
KW - surveillance
UR - http://www.scopus.com/inward/record.url?scp=85152543768&partnerID=8YFLogxK
U2 - 10.3389/fonc.2023.1139940
DO - 10.3389/fonc.2023.1139940
M3 - Article
C2 - 37035171
AN - SCOPUS:85152543768
SN - 2234-943X
VL - 13
SP - 1139940
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1139940
ER -