Skip to search boxSkip to navigationSkip to main content

Evaluation of a Streamlined Oncologist-Led BRCA Mutation Testing and Counseling Model for Patients With Ovarian Cancer

  • Nicoletta Colombo(corresponding author)
    ,
  • Gloria Huang
    ,
  • Giovanni Scambia
    ,
  • Eva Chalas
    ,
  • Sandro Pignata
    ,
  • James Fiorica
*Corresponding author for this work
  • University of Milan - Bicocca
    ,
  • Yeshiva University
    ,
  • Catholic University of the Sacred Heart
    ,
  • Winthrop University Hospital
    ,
  • IRCCS Istituto nazionale tumori Fondazione Giovanni Pascale - Napoli
    ,
  • Sarasota Memorial Hospital
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Purpose There is a growing demand for BRCA1/2 mutation (BRCAm) testing in patients with ovarian cancer; however, the limited number of genetic counselors presents a potential barrier. To facilitate more widespread BRCAm testing in ovarian cancer, pretest counseling by the oncology team could shorten testing turnaround times and ease the pressure on genetic counselors. Patients and Methods The prospective, observational Evaluating a Streamlined Onco-genetic BRCA Testing and Counseling Model Among Patients With Ovarian Cancer (ENGAGE) study evaluated a streamlined, oncologist-led BRCAm testing pathway. The analysis population comprised 700 patients with ovarian cancer at 26 sites in the United States, Italy, and Spain. The primary objectives were to assess turnaround time and, using questionnaires, to evaluate stakeholder satisfaction (patients, oncologists, and geneticists or genetic counselors) with the oncologist-led BRCAm testing pathway. Results The median overall turnaround time was 9.1 weeks (range, 0.9 to 37.1 weeks), with median turnaround times in the United States, Italy, and Spain of 4.1 weeks (range, 0.9 to 37.1 weeks), 20.4 weeks (range, 2.9 to 35.4 weeks), and 12.0 weeks (range, 2.0 to 36.7 weeks), respectively. Patient satisfaction with the oncologist-led BRCAm testing pathway was high, with . 99% of patients expressing satisfaction with pre- and post-BRCAm test counseling. Oncologist satisfaction with the BRCAm testing pathway was also high, with . 80% agreeing that the process for performing BRCAm testing worked well and that counseling patients on BRCAm testing was an efficient use of their time. Oncologists expressed higher levels of satisfaction with the BRCAm testing pathway than did geneticists or genetic counselors. Conclusion The results of the ENGAGE study demonstrate that an oncologist-led BRCAm testing process is feasible in ovarian cancer. Development of local BRCAm testing guidelines similar to the one used in this study could allow faster treatment decisions and better use of resources in the management of patients with ovarian cancer.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1300-1307 (8 pages)

Journal (Volume, Issue Number)

Journal of Clinical Oncology (Volume 36, Issue 13)

Publication milestones

  • Published - 05/01/2018

Publication status

Published - 05/01/2018

ISSN

0732-183X

Publication IDs

  • Scopus: 85046007455
  • PubMed: 29558274

Publication metrics

Metrics

SciVal
citations
39
Fractional count
1
Fractional count
0.06
Fractional count
15
Fractional count
0.94
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
3.37
SciVal
Author count
16
SciVal
Paper percentile
97
SciVal
Top percentile
5

PlumX, opens in new tab

Mentions
3
Captures
84
Citation count
93

Funding Details

We thank the following ENGAGE study co-investigators who contributed to patient recruitment and data collection: Italy: Laura Cortesi (University Hospital Azienda Ospedaliero-Universitaria Policlinico di Modena), Sabino De Placido (Università Federico II di Napoli), Serafina Mammoliti (IRCCS Hospital San Martino), Franco Odicino (University of Brescia), and Paolo Zola (University of Turin); Spain: José Ángel Arranz Arija (Hospital Gregorio Marañón), Alfonso Yubero Esteban (Hospital Clínico Universitario Lozano Blesa), Tomás Pascual (Hospital La Princesa), and Andrés Redondo (Hospital Universitario La Paz); United States: John Chan (California Pacific Medical Center Research Institute/Palo Alto Medical Foundation), Paul DiSilvestro (Women and Infants Hospital), Veena John (Monter Cancer Center, NS-LIJHS), Donna McNamara (Hackensack University Medical Center), and Susan Zweizig (University of Massachusetts Memorial Medical Center). We thank Nazneen Rahman (Institute of Cancer Research, London), who contributed to the study design and data review; Ilian Tchakov and Jerzy Tyczynski (formerly AstraZeneca), who contributed to the study design; Alvin Milner (AstraZeneca), who contributed to data review and manuscript preparation; and Kamil Jedynski, Yasmina Tazir, and Hilary Bagguley (AstraZeneca), who contributed to study management and execution. Writing assistance was provided by Gillian Keating from Mudskipper Business Limited, funded by AstraZeneca. Current affiliation for Gloria Huang is Yale School of Medicine and Yale Cancer Center, New Haven, CT, and current affiliation for Sudeep Karve is AbbVie Inc, North Chicago, IL.
FundersFunding number
NCI
P30CA016086
ACC
-
UNINA
-
IRCCS Fondazione Policlinico San Matteo - Pavia
-
UMMS
-
MMCRI
-
Azienda Ospedaliero Universitaria Maggiore della Carità
-
ICR
-