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Prescribers and patients drive maintenance therapy patterns in a community oncology practice: National guidelines versus the real-world experience.
Chase, Dana M; Iadeluca, Laura; Lim, Jonathan; Tseng, Wan-Yu; Bulsara, Purva; Patton, Gregory.
Afiliação
  • Chase DM; University of California, Los Angeles, 100 UCLA Medical Plaza, Suite 383, Los Angeles, CA 90024, USA.
  • Iadeluca L; GSK, 2929 Walnut Street, Ste. 1700, Philadelphia, PA 19104, USA.
  • Lim J; GSK, 2929 Walnut Street, Ste. 1700, Philadelphia, PA 19104, USA.
  • Tseng WY; Ontada, 33 Arch Street, 20th Floor, Boston, MA 02110, USA.
  • Bulsara P; Ontada, 33 Arch Street, 20th Floor, Boston, MA 02110, USA.
  • Patton G; Ontada, 33 Arch Street, 20th Floor, Boston, MA 02110, USA.
Gynecol Oncol Rep ; 54: 101440, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39040942
ABSTRACT

Objective:

Previous studies have shown that first-line (1L) maintenance therapy (MT) with poly(ADP-ribose) polymerase inhibitors and/or bevacizumab improves outcomes among patients with advanced ovarian cancer (OC); however, these treatments are underutilized. This study aimed to provide a real-world understanding of MTs among patients with advanced OC who received 1L platinum-based chemotherapy (PBC).

Methods:

A retrospective chart review using iKnowMed electronic health records to identify patients aged ≥18 years with advanced OC who initiated 1L PBC between January 1, 2018-December 31, 2020. Following 1L PBC, patients could have received MT or active surveillance (AS). Kaplan-Meier methods were used to estimate time to treatment discontinuation (TTD), real-world progression-free survival (rwPFS), and overall survival (OS).

Results:

Of the 600 chart-reviewed patients included, 239 (39.8 %) received MT and 315 (52.5 %) received AS. Patients who were <65 years of age, or those with higher-stage disease or those who had received neoadjuvant treatment, were more likely to initiate MT than AS. Genetic testing rates were low across both cohorts. Median (95 % confidence interval [CI]) TTD for the MT cohort was 13.6 months (11.0, 21.2). Median (95 % CI) rwPFS was 26.9 months (21.3, not reached) and 11.3 months (9.5, 13.0) for the 1L MT and AS cohorts, respectively (p < 0.0001). OS at 36 months was 82.4 % in the 1L MT cohort and 58.0 % in the 1L AS cohort.

Conclusions:

This study reinforces clinical trial findings that 1L MT improves outcomes in patients with advanced OC; however, genetic testing rates and 1L MT remained low.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article