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Barriers to Prescribing Targeted Therapies for Patients With NSCLC With Highly Actionable Gene Variants in the Veterans Affairs National Precision Oncology Program.
Vashistha, Vishal; Armstrong, Jenna; Winski, David; Poonnen, Pradeep J; Hintze, Bradley; Price, Meghan; Snowdon, Jane L; Weeraratne, Dilhan; Brotman, David; Jackson, Gretchen P; Kelley, Michael J.
Afiliação
  • Vashistha V; Raymond G. Murphy New Mexico Veterans Affairs Medical Center, Section of Hematology/Oncology, Albuquerque, NM.
  • Armstrong J; Durham Veterans Affairs Medical Center, Division of Hematology and Oncology, Durham, NC.
  • Winski D; National Oncology Program Office, Department of Veterans Affairs, Durham, NC.
  • Poonnen PJ; Duke University School of Medicine, Durham, NC.
  • Hintze B; Veterans Affairs Boston Healthcare System, Jamaica Plan Campus, Boston, MA.
  • Price M; Durham Veterans Affairs Medical Center, Division of Hematology and Oncology, Durham, NC.
  • Snowdon JL; National Oncology Program Office, Department of Veterans Affairs, Durham, NC.
  • Weeraratne D; Duke University School of Medicine, Durham, NC.
  • Brotman D; Duke University Health System, Divisions of Medical Oncology, Hematology, Hematologic Malignancies and Cell Therapeutics, Durham, NC.
  • Jackson GP; Duke University School of Medicine, Durham, NC.
  • Kelley MJ; Durham Veterans Affairs Medical Center, Division of Hematology and Oncology, Durham, NC.
JCO Oncol Pract ; 17(7): e1012-e1020, 2021 07.
Article em En | MEDLINE | ID: mdl-33780286
ABSTRACT

PURPOSE:

Next-generation sequencing (NGS) gene panels are frequently completed for patients with advanced non-small-cell lung cancer (NSCLC). Patients with highly actionable gene variants have improved outcomes and reduced toxicities with the use of corresponding targeted agents. We sought to identify barriers to targeted agent use within the Veterans Health Affairs' National Precision Oncology Program (NPOP).

METHODS:

A retrospective evaluation of patients with NSCLC who underwent NGS multigene panels through NPOP between July 2015 and February 2019 was conducted. Patients who were assigned level 1 or 2A evidence for oncogenic gene variants by an artificial intelligence offering (IBM Watson for Genomics [WfG]) and NPOP staff were selected. Antineoplastic drug prescriptions and provider notes were reviewed. Reasons for withholding targeted treatments were categorized.

RESULTS:

Of 1,749 patients with NSCLC who successfully underwent NGS gene panel testing, 112 (6.4%) patients were assigned level 1 and/or 2A evidence for available targeted treatments by WfG and NPOP staff. All highly actionable gene variants were within ALK, BRAF, EGFR, ERBB2, MET, RET, and ROS1. Of these, 36 (32.1%) patients were not prescribed targeted agents. The three most common reasons were (1) patient did not carry a diagnosis of metastatic disease (33.3%), (2) treating provider did not comment on the NGS results (25.0%), and (3) provider felt that patient could not tolerate therapy (19.4%). No patients were denied access to level 1 or 2A targeted drugs because of rejection of a nonformulary drug request.

CONCLUSION:

A substantial minority of patients with NSCLC bearing highly actionable gene variants are not prescribed targeted agents. Further provider- and pathologist-directed educational efforts and implementation of health informatics systems to provide real-time decision support for test ordering and interpretation are needed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veteranos / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Oncol Pract Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veteranos / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Oncol Pract Ano de publicação: 2021 Tipo de documento: Article