Treatment patterns among patients with advanced/recurrent endometrial cancer in the United States.

Authors

null

Jinan Liu

GlaxoSmithKline, Navy Yard, PA

Jinan Liu, Eric M Maiese, Bruno Émond, Marie-Hélène Lafeuille, Patrick Lefebvre, Isabelle Ghelerter, Caterina Wu, Jean Hurteau, Premal H. Thaker

Organizations

GlaxoSmithKline, Navy Yard, PA, Analysis Group, Montreal, QC, Canada, Analysis Group, Inc., Montreal, QC, Canada, Analysis Group, Inc., Menlo Park, CA, GlaxoSmithKline, Waltham, MA, Department of Gynecologic Oncology, Washington University School of Medicine, St. Louis, MO

Research Funding

Pharmaceutical/Biotech Company
GlaxoSmithKline

Background: Among patients (pts) with endometrial cancer (EC), response rates for platinum-based regimens in the first-line (1L) setting range from 40% to 62% in clinical trials. This study describes patient characteristics, treatment patterns, time to next treatment (TTNT), and overall survival (OS) among pts with advanced/recurrent EC treated with a platinum-based regimen in a real-world setting in the US. Methods: This retrospective study used Optum Clinformatics Extended Data Mart de-identified databases from January 1, 2007, to December 31, 2019. Adult pts with advanced/recurrent EC who initiated a 1L platinum-based regimen and subsequently initiated second-line (2L) antineoplastic therapy were identified. Prior to initiation of 1L, a 12-month washout period of continuous enrollment without use of antineoplastic agents (except hormonal agents) was imposed. Kaplan-Meier (KM) rates were used to report TTNT and OS from 2L, third line (3L), and fourth line (4L), separately. Results: A total of 1878 pts with advanced/recurrent EC initiated 2L therapy following a platinum-based regimen in 1L. Among them, 739 (39.4%) pts initiated 3L and 330 (17.6%) initiated 4L or later (4L+) therapy. Median pt age was 68.0 years. More pts received platinum-based regimens (56.4%) in 2L than other options (Table). Few pts (3.3%) received immunotherapy. Among pts receiving 3L, a similar percentage of pts were treated with platinum-based (33.2%) and other chemotherapy regimens (33.8%); few pts received immunotherapy (3.0%). Among pts receiving 4L+, the most frequent treatment option was other chemotherapy (46.1%). Median TTNT was 17.7, 10.6, and 8.4 months for 2L, 3L, and 4L pts, respectively. KM rates of OS following initiation of 2L therapy at 1, 2, 3, and 4 years were 68.4%, 49.6%, 41.3%, and 33.6%, respectively, with a median OS of 23.5 months. Conclusions: Among pts with advanced/recurrent EC treated with platinum-based therapy in 1L, platinum-based regimens remain prevalent treatment choices in later lines of therapy. In this study, immunotherapy was used infrequently in 2L, 3L, and 4L+. The median TTNT decreased in later lines of therapy. This study highlights a critical need for novel, more effective treatment options in later lines of therapy to optimize outcomes among pts with advanced/recurrent EC.


1L

n = 1878
2L

n = 1878
3L

n = 739
4L+

n = 330
Duration of treatment, mean ± StDev (median), months
4.5±3.0

(4.4)
4.1±4.0

(3.1)
4.5±4.8

(3.2)
3.8±3.2

(3.1)
Duration of treatment-free interval, mean ± StDev (median), months
8.0±13.3

(3.5)
10.0±19.5

(2.1)
4.0±10.6

(0.5)
2.8±8.1

(0.4)
Treatment option, %

Platinum-based regimen

Other chemotherapy

Targeted therapy

NCCN-recommended immunotherapy

Other immunotherapy


100










56.4

21.8

9.6

3.1

0.2


33.2

33.8

17.1

2.7

0.3


31.5

46.1

32.4

7.9


Median TTNT, months

17.7
10.6
8.4

NCCN, National Comprehensive Cancer Network; StDev, standard deviation.

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Abstract Details

Meeting

2021 ASCO Quality Care Symposium

Session Type

Poster Session

Session Title

Poster Session B: Patient Experience; Quality, Safety, and Implementation Science; Technology and Innovation in Quality of Care

Track

Technology and Innovation in Quality of Care,Patient Experience,Quality, Safety, and Implementation Science,Cost, Value, and Policy,Health Care Access, Equity, and Disparities

Sub Track

Real-World Evidence

Clinical Trial Registration Number

OneCDP#213577

Citation

J Clin Oncol 39, 2021 (suppl 28; abstr 291)

DOI

10.1200/JCO.2020.39.28_suppl.291

Abstract #

291

Poster Bd #

Online Only

Abstract Disclosures