AI Article Synopsis

  • The study evaluates national compliance with the Cancer Program Practice Profile Reports (CP3R) metrics, focusing on the use of combination chemotherapy or chemo-immunotherapy for certain breast cancer patients within 120 days of diagnosis.
  • An analysis of data from the National Cancer Database shows an increase in treatment concordance from 75.7% in 2004 to 89.5% in 2014, with better overall survival for patients receiving recommended treatments.
  • Patients treated at academic hospitals and those with private insurance experienced greater survival benefits, highlighting the importance of accessibility to high-quality care.

Article Abstract

Background: Cancer Program Practice Profile Reports (CP3R) metrics were released by the Commission on Cancer to provide standards for high-quality care. One metric is the recommendation of combination chemotherapy or chemo-immunotherapy (CIT) within 120 days of diagnosis for women under 70 with AJCC T1cN0M0 or Stage IB-III HER2+ or hormone receptor negative breast cancer ([Multi-agent chemotherapy] MAC). Our study assesses national concordance rates for MAC and CIT.

Methods: The National Cancer Database was queried from 2004-2014.

Results: 122,045 patients met criteria, of whom treatment for 101,800 (83.4%) patients was concordant with MAC and CIT. Treatment concordance increased from 75.7% in 2004 to 89.5% in 2014. For HER2+ patients, use of CIT treatment downtrended with progression of pathological stage, from 70.1% (stage I) to 58.1% (stage III). Mean overall survival of patients whose treatment was concordant with MAC and CIT was longer than that of patients who were non-concordant (146.6 vs 143.8 months, <.01). On Cox regression, there was a survival benefit for concordant patients who were treated at academic hospitals (HR .89, 95% CI 0.802-.976) and had private insurance (HR .76, 95% CI 0.65-.89).

Conclusion: Compliance with MAC and CIT has improved over the past decade and is associated with a significant improvement in overall survival.

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Source
http://dx.doi.org/10.1177/00031348211051674DOI Listing

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