TY - JOUR
T1 - Real-world Treatment Patterns and Clinical Outcomes Across Lines of Therapy in Patients With Advanced/Metastatic Gastric or Gastroesophageal Junction Cancer
AU - Le, Dung T.
AU - Ott, Patrick A.
AU - Korytowsky, Beata
AU - Le, Hannah
AU - Le, T. Kim
AU - Zhang, Ying
AU - Maglinte, Gregory A.
AU - Abraham, Pranav
AU - Patel, Dhiren
AU - Shangguan, Tong
AU - Chau, Ian
N1 - Funding Information:
D.T. Le has received research funding from, and participated in advisory boards for, Bristol-Myers Squibb and Merck Serono, and has received speaker's honoraria from Merck Serono. P.A. Ott has received research funding and/or consultancy fees from Amgen, ARMO Biosciences, Array, AstraZeneca, Bristol-Myers Squibb, Celldex, CytomX, Genentech, Merck Serono, Neon Therapeutics, Novartis, and Pfizer. B. Korytowsky, T.K. Le, Y. Zhang, P. Abraham, D. Patel, and T. Shangguan are employees of, and hold stock in, Bristol-Myers Squibb. H. Le and G.A. Maglinte were employed by Bristol-Myers Squibb at the time of analysis. I. Chau has participated in advisory boards for AstraZeneca, Bayer, Bristol-Myers Squibb, Eli Lilly, Five Prime Therapeutics, Merck Serono, MSD, Oncologie International, Pierre Fabre, and Roche, and received honorarium and/or research funding from Eli Lilly, Janssen-Cilag, Merck Serono, and Sanofi.This study was sponsored by Bristol-Myers Squibb. Medical writing assistance was provided by Martin Bell, PhD, of Evidence Scientific Solutions, and was funded by Bristol-Myers Squibb. Hannah Le and Gregory A. Maglinte were employees of Bristol-Myers Squibb at the time of the analysis.
Funding Information:
D.T. Le has received research funding from, and participated in advisory boards for, Bristol-Myers Squibb and Merck Serono , and has received speaker’s honoraria from Merck Serono. P.A. Ott has received research funding and/or consultancy fees from Amgen , ARMO Biosciences , Array , AstraZeneca , Bristol-Myers Squibb , Celldex , CytomX , Genentech , Merck Serono , Neon Therapeutics , Novartis , and Pfizer . B. Korytowsky, T.K. Le, Y. Zhang, P. Abraham, D. Patel, and T. Shangguan are employees of, and hold stock in, Bristol-Myers Squibb. H. Le and G.A. Maglinte were employed by Bristol-Myers Squibb at the time of analysis. I. Chau has participated in advisory boards for AstraZeneca, Bayer, Bristol-Myers Squibb, Eli Lilly, Five Prime Therapeutics, Merck Serono, MSD, Oncologie International, Pierre Fabre, and Roche, and received honorarium and/or research funding from Eli Lilly , Janssen-Cilag , Merck Serono , and Sanofi .
Publisher Copyright:
© 2019 The Authors
PY - 2020/3
Y1 - 2020/3
N2 - Background: First-line (1L) and second-line (2L) therapies for advanced/metastatic gastric cancer (GC) and gastroesophageal junction cancer (GEJC) have modest efficacy, and therapeutic options in subsequent lines are limited as disease progresses. We assessed real-world treatment patterns and outcomes for advanced/metastatic GC/GEJC. Patients and Methods: Adult patients diagnosed with advanced/metastatic GC/GEJC between January 1, 2011 and April 30, 2018 were identified using the Flatiron Health database. Median overall survival (OS) from start of each line of therapy until death was estimated by the Kaplan-Meier method. Duration of therapy (DoT) was time from start date until end date of each line. Results: We identified 3291 patients with advanced/metastatic GC/GEJC adenocarcinoma. At diagnosis, the median age was 68 years, 60% were white, 53% had initial stage IV disease, and 57% had GC. Of these 3291 patients, most (75%) received at least 1 therapy; 32% received 2L, 14% received third-line (3L) therapy, and 6% received at least 4 lines of therapy (4L+). The median OS from start of 1L was 10.7 months (2L, 7.6 months; 3L, 6.1 months; 4L+, 2.8 months). The median DoT in 1L was 2.2 months (2L, 2.1 months; 3L, 1.7 months; 4L+, 3.0 months). Use of targeted and immunotherapies generally increased progressively with each subsequent line of therapy. Conclusion: One-quarter of patients with advanced/metastatic GC/GEJC remained untreated, and only approximately one-half of patients receiving 1L therapy received subsequent treatment. In all lines of therapy, OS was generally poor and DoT was short. More effective treatment options are needed across all lines of therapy for this highly burdensome disease.
AB - Background: First-line (1L) and second-line (2L) therapies for advanced/metastatic gastric cancer (GC) and gastroesophageal junction cancer (GEJC) have modest efficacy, and therapeutic options in subsequent lines are limited as disease progresses. We assessed real-world treatment patterns and outcomes for advanced/metastatic GC/GEJC. Patients and Methods: Adult patients diagnosed with advanced/metastatic GC/GEJC between January 1, 2011 and April 30, 2018 were identified using the Flatiron Health database. Median overall survival (OS) from start of each line of therapy until death was estimated by the Kaplan-Meier method. Duration of therapy (DoT) was time from start date until end date of each line. Results: We identified 3291 patients with advanced/metastatic GC/GEJC adenocarcinoma. At diagnosis, the median age was 68 years, 60% were white, 53% had initial stage IV disease, and 57% had GC. Of these 3291 patients, most (75%) received at least 1 therapy; 32% received 2L, 14% received third-line (3L) therapy, and 6% received at least 4 lines of therapy (4L+). The median OS from start of 1L was 10.7 months (2L, 7.6 months; 3L, 6.1 months; 4L+, 2.8 months). The median DoT in 1L was 2.2 months (2L, 2.1 months; 3L, 1.7 months; 4L+, 3.0 months). Use of targeted and immunotherapies generally increased progressively with each subsequent line of therapy. Conclusion: One-quarter of patients with advanced/metastatic GC/GEJC remained untreated, and only approximately one-half of patients receiving 1L therapy received subsequent treatment. In all lines of therapy, OS was generally poor and DoT was short. More effective treatment options are needed across all lines of therapy for this highly burdensome disease.
KW - Chemotherapies
KW - Gastric cancer
KW - Immunotherapy
KW - Observational
KW - Utilization patterns
UR - http://www.scopus.com/inward/record.url?scp=85076240337&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076240337&partnerID=8YFLogxK
U2 - 10.1016/j.clcc.2019.09.001
DO - 10.1016/j.clcc.2019.09.001
M3 - Article
C2 - 31813769
AN - SCOPUS:85076240337
SN - 1533-0028
VL - 19
SP - 32-38.e3
JO - Clinical colorectal cancer
JF - Clinical colorectal cancer
IS - 1
ER -