TY - JOUR
T1 - Outcomes in Patients With Non–small-cell Lung Cancer With Brain Metastases Treated With Pembrolizumab-based Therapy
AU - Sun, Lova
AU - Davis, Christiana W.
AU - Hwang, Wei Ting
AU - Jeffries, Seth
AU - Sulyok, Lydia Frenzel
AU - Marmarelis, Melina E.
AU - Singh, Aditi P.
AU - Berman, Abigail T.
AU - Feigenberg, Steven J.
AU - Levin, William
AU - Ciunci, Christine A.
AU - Bauml, Joshua M.
AU - Cohen, Roger B.
AU - Langer, Corey J.
AU - Aggarwal, Charu
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/1
Y1 - 2021/1
N2 - Background: Patients with metastatic non–small-cell lung cancer (mNSCLC) and untreated brain metastases (BM) have been excluded from most trials of immune checkpoint inhibitors (ICIs). Real-world evidence on efficacy and survival outcomes of ICIs in patients with BM is limited. Patients and Methods: We conducted a single-center retrospective study of patients with mNSCLC treated with pembrolizumab with or without chemotherapy and compared progression-free survival (PFS) and overall survival (OS) between patients with and without BM using Kaplan-Meier and Cox methodology. We also characterized systemic and intracranial objective response rate (ORR) and treatment details, including timing of cranial irradiation. Results: Between Augutst 2013 and December 2018, 570 patients with mNSCLC treated with pembrolizumab-based therapy were analyzed. Of 126 (22.1%) patients with BM, 96 (76.2%) had treated BM (local therapy prior to pembrolizumab), and 30 (23.8%) had untreated BM. Of patients with untreated BM, 17 (56.7%) underwent radiation within 30 days after pembrolizumab initiation. In the remaining 13 (43.3%) treated with pembrolizumab-based therapy alone, intracranial ORR was 36.4%. Patients with and without BM did not have significantly different systemic ORR (27.8% vs. 29.7%; P = .671), PFS (mPFS 9.2 vs. 7.7 months; P = .609), or OS (mOS 18.0 vs. 18.7 months; P = .966). Factors associated with improved survival on Cox analysis included female gender, performance status, adenocarcinoma histology, and first-line therapy. Conclusions: Patients with BM did not have inferior survival to patients without BM after treatment with pembrolizumab-based therapy. In the current era, BM may not automatically confer inferior survival, and should not exclude patients from receiving pembrolizumab-based therapy.
AB - Background: Patients with metastatic non–small-cell lung cancer (mNSCLC) and untreated brain metastases (BM) have been excluded from most trials of immune checkpoint inhibitors (ICIs). Real-world evidence on efficacy and survival outcomes of ICIs in patients with BM is limited. Patients and Methods: We conducted a single-center retrospective study of patients with mNSCLC treated with pembrolizumab with or without chemotherapy and compared progression-free survival (PFS) and overall survival (OS) between patients with and without BM using Kaplan-Meier and Cox methodology. We also characterized systemic and intracranial objective response rate (ORR) and treatment details, including timing of cranial irradiation. Results: Between Augutst 2013 and December 2018, 570 patients with mNSCLC treated with pembrolizumab-based therapy were analyzed. Of 126 (22.1%) patients with BM, 96 (76.2%) had treated BM (local therapy prior to pembrolizumab), and 30 (23.8%) had untreated BM. Of patients with untreated BM, 17 (56.7%) underwent radiation within 30 days after pembrolizumab initiation. In the remaining 13 (43.3%) treated with pembrolizumab-based therapy alone, intracranial ORR was 36.4%. Patients with and without BM did not have significantly different systemic ORR (27.8% vs. 29.7%; P = .671), PFS (mPFS 9.2 vs. 7.7 months; P = .609), or OS (mOS 18.0 vs. 18.7 months; P = .966). Factors associated with improved survival on Cox analysis included female gender, performance status, adenocarcinoma histology, and first-line therapy. Conclusions: Patients with BM did not have inferior survival to patients without BM after treatment with pembrolizumab-based therapy. In the current era, BM may not automatically confer inferior survival, and should not exclude patients from receiving pembrolizumab-based therapy.
KW - Adenocarcinoma of Lung/drug therapy
KW - Aged
KW - Antibodies, Monoclonal, Humanized/therapeutic use
KW - Antineoplastic Agents, Immunological/therapeutic use
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
KW - Brain Neoplasms/drug therapy
KW - Carcinoma, Non-Small-Cell Lung/drug therapy
KW - Carcinoma, Squamous Cell/drug therapy
KW - Female
KW - Follow-Up Studies
KW - Humans
KW - Lung Neoplasms/drug therapy
KW - Lymphatic Metastasis
KW - Male
KW - Middle Aged
KW - Prognosis
KW - Retrospective Studies
KW - Survival Rate
UR - http://www.scopus.com/inward/record.url?scp=85097385257&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2020.10.017
DO - 10.1016/j.cllc.2020.10.017
M3 - Article
C2 - 33279417
AN - SCOPUS:85097385257
SN - 1525-7304
VL - 22
SP - 58-66.e3
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 1
ER -