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Effectiveness research in oncology with electronic health record data: A retrospective cohort study emulating the PALOMA-2 trial.
Merola, David; Young, Jessica; Schrag, Deborah; Lin, Kueiyu Joshua; Alwardt, Sarah; Schneeweiss, Sebastian.
Afiliação
  • Merola D; Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Young J; Department of Epidemiology, Harvard TH Chan School of Public Health, Boston, Massachusetts, USA.
  • Schrag D; Department of Epidemiology, Harvard TH Chan School of Public Health, Boston, Massachusetts, USA.
  • Lin KJ; Department of Population Medicine, Harvard Medical School & Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.
  • Alwardt S; CAUSALab, Harvard TH Chan School of Public Health, Boston, Massachusetts, USA.
  • Schneeweiss S; Department of Medicine, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical School, New York, New York, USA.
Pharmacoepidemiol Drug Saf ; 32(4): 426-434, 2023 04.
Article em En | MEDLINE | ID: mdl-36345809
ABSTRACT

PURPOSE:

Oncology electronic health record (EHR) databases have increased in quality and availability over the past decade, yet it remains unclear whether these clinical practice data can be used to conduct reliable comparative effectiveness studies. We sought to emulate a clinical trial with EHR data in the advanced breast cancer population and compare our results against the trial.

METHODS:

This cohort study used EHR data from US oncology practices. All elements of the study were defined to mimic the PALOMA-2 trial as closely as possible. Patients with hormone-positive, HER-2 negative metastatic breast cancer with no prior treatment for metastatic disease were included. Patients initiating palbociclib and letrozole on the same day following the earliest record of metastasis were compared to those initiating letrozole only. The primary associational measure was the conditional hazard ratio for time-to-next treatment (TTNT). TTNT is well-measured in our data source and amenable for calibration against the randomized study results of the PALOMA-2 trial. We used multiple imputation for several patient characteristics with missing values.

RESULTS:

There were 3836 study-eligible women with advanced breast cancer. The hazard ratio for TTNT in the observational study (HR 0.62; 95% CI 0.56-0.68) was closely aligned with that of the randomized trial (HR 0.64; 95% CI 0.52-0.78).

CONCLUSIONS:

Under our assumptions on missing data and comparability of the two study populations, results from our non-randomized study closely matched that of the randomized trial. Further studies are needed to determine whether EHR data can yield reliable conclusions on treatment effects in oncology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Registros Eletrônicos de Saúde Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Pharmacoepidemiol Drug Saf Assunto da revista: EPIDEMIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Registros Eletrônicos de Saúde Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Pharmacoepidemiol Drug Saf Assunto da revista: EPIDEMIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos