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Rates of genetic consultation in high-grade serous ovarian cancer patients in the era of PARP inhibitor therapy: A population-based study.
Brent, Shannon E; McGee, Jacob; Vicus, Danielle; Kim, Raymond; Eisen, Andrea; Wilton, Andrew S; Gien, Lilian T.
Afiliación
  • Brent SE; Department of Obstetrics and Gynaecology, University of Toronto, Toronto, Ontario, Canada.
  • McGee J; Department of Obstetrics and Gynaecology, Western University, London, Ontario, Canada.
  • Vicus D; Department of Obstetrics and Gynaecology, University of Toronto, Toronto, Ontario, Canada.
  • Kim R; Division of Gynecologic Oncology, Sunnybrook Odette Cancer Center, Toronto, Ontario, Canada.
  • Eisen A; Division of Medical Oncology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Wilton AS; Department of Medical Oncology, Sunnybrook Health Sciences Centre, Odette Cancer Centre, Toronto, Ontario, Canada.
  • Gien LT; ICES Research, Toronto, Ontario, Canada.
Int J Gynaecol Obstet ; 166(1): 282-289, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38284267
ABSTRACT

OBJECTIVE:

The American Society of Clinical Oncology recommends all patients with high-grade serous ovarian carcinoma (HGSC) undergo germline genetic testing. Genetic consultation rates in Ontario, Canada, only reached 13.3% in 2011. In 2016, PARP inhibitor maintenance therapy became available in Ontario for BRCA-positive HGSC patients. Given expanding treatment options, we re-examined genetic consultation rates among HGSC patients.

METHODS:

This retrospective cohort study identified patients diagnosed with HGSC between 2012 and 2019 using population-based administrative data from Ontario. Genetics consultations were identified using Ontario Health Insurance Plan billing codes. Consultation rates over time were analyzed using Cochran-Armitage trend test and segmental regression analysis. Multivariable analysis identified factors associated with attending genetics consultation.

RESULTS:

This study included 4645 HGSC patients. The mean age was 64.2 years (±SD 12.3); 56.3% had stage 3-4 disease. Overall, approximately 35% attended genetics consultations. The genetic consultation rate per year increased significantly from 21.6% to 42.6% (P < 0.001). Shorter times between diagnosis and genetics consult were observed after PARP inhibitors became available (68.1 vs 34.1 weeks, P < 0.001). Patients treated at designated cancer centers (odds ratio [OR] 2.11, P < 0.001), diagnosed in later years (OR 1.33, P < 0.001), and from higher income groups (P < 0.05) were more likely to attend genetics consultation; older patients were less likely (OR 0.98, P < 0.001). After PARP inhibitors became available, consultation rates plateaued (P < 0.001).

CONCLUSIONS:

Between 2012 and 2019, genetic consultation rates improved significantly among HGSC patients; however, a large proportion of patients never attended consultation. Further exploration of barriers to care is warranted to improve consultation rates and ensure equitable access to care.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Derivación y Consulta / Cistadenocarcinoma Seroso / Inhibidores de Poli(ADP-Ribosa) Polimerasas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: America do norte Idioma: En Revista: Int J Gynaecol Obstet / Int. j. gynaecol. obstet / International journal of gynaecology and obstetrics Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Derivación y Consulta / Cistadenocarcinoma Seroso / Inhibidores de Poli(ADP-Ribosa) Polimerasas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: America do norte Idioma: En Revista: Int J Gynaecol Obstet / Int. j. gynaecol. obstet / International journal of gynaecology and obstetrics Año: 2024 Tipo del documento: Article