Breast Cancer Patients Fare Worse When Adjuvant Chemotherapy Is Delayed

Publication
Article
Oncology & Biotech NewsMarch 2014
Volume 8
Issue 3

Breast cancer patients whose chemotherapy is initiated >60 days following surgery experience worse survival outcomes

Mariana Chavez-MacGregor, MD

Breast cancer patients whose chemotherapy is initiated >60 days following surgery experience worse survival outcomes, according to a large, retrospective review of patient medical records conducted by Mariana Chavez-MacGregor, MD, and her colleagues at The University of Texas MD Anderson Cancer Center. The impact of treatment delay is greatest among patients with stage III or triple-negative breast cancer (TNBC) and those whose HER2-positive tumors have been treated with trastuzumab.

Most adjuvant breast cancer chemotherapy begins within a few weeks of surgery; however, previous research results differ on the impact that longer time to chemotherapy (TTC) might have on survival. Treatment delays also have been reported to occur more frequently among low-income groups, racial minorities, and Medicare patients.

To further investigate the impact of TTC, Chavez-MacGregor, an assistant professor in the department of Breast Medical Oncology, Division of Cancer Medicine, at MD Anderson, and colleagues analyzed the records of 6827 patients diagnosed with stage I to III invasive primary breast cancer who received treatment at the cancer center between 1997 and 2011. Most patients had stage I/II disease (84.3%) and 15.5% had stage III.

Patient medical records were divided into three groups based on the number of days between completion of surgery and start of chemotherapy: ≤30 days (n = 2716), 31 to 60 days (n = 2994), and ≥61 days (n = 1117). Overall survival (OS), relapse-free survival (RFS), and distant relapse-free survival (DRFS) were assessed for the study population as a whole and also according to breast cancer subtype, with a median follow- up of 59.3 months.

Investigators applied multivariable models and adjusted for confounders to estimate 5-year OS, RFS, and DRFS for all patients based on TTC and other patient characteristics. They determined that when compared with patients who had adjuvant chemotherapy ≤30 days after surgery, patients whose TTC was ≥61 days post-surgery had a 19% increased risk of death (HR = 1.19; 95% CI, 1.02-1.38).

Although TTC was not significantly linked to outcome in patients with stage I disease, the risk of distant relapse was estimated to increase by 18% in stage II patients whose chemotherapy started 31 to 60 days after surgery, and by 20% in the ≥61 days cohort. For patients with stage III disease who started chemotherapy ≥61 days after surgery, the risk of death was increased by 76%, the risk of relapse by 34%, and the risk of distant relapse by 36%, when compared with patients whose TTC was ≤30 days.

The impact of TTC on survival and relapse also varied according to breast cancer subtype. Patients with hormone receptor (HR)-positive tumors receiving chemotherapy ≥61 days after surgery had a 29% increased risk of death (HR = 1.29; 95% CI, 1.02-1.64).

HR-positive patients who received chemotherapy 31 to 60 days after surgery were estimated to have a 15% increased risk of relapse and an 18% increased risk of distant relapse, compared with patients whose TTC was ≤30 days, the researchers reported.

The magnitude of risk was more pronounced when the researchers looked at the records of patients with TNBC and those who were HER2-positive and treated with trastuzumab.

Patients with TNBC who received chemotherapy either 31 to 60 days or ≥61 days after surgery had a 74% and 54% increased risk of death, respectively, compared with the ≤30 days group, but RFS and DRFS were not impacted by TTC in these patients.

For patients who were HER2-positive but not treated with trastuzumab (n = 551), outcomes were not adversely affected by longer TTC, but a statistically significant increase in death risk was observed in the trastuzumab- treated group (n = 591) when chemotherapy was initiated ≥61 days after surgery versus ≤30 days (HR = 3.09; 95% CI, 1.49-6.39). A trend toward worse RFS and DRFS was also reported for this group.

The researchers concluded that for patients with stage II and III breast cancer, those with TNBC, and those with HER2-positive tumors, “Every effort should be made to avoid postponing the initiation of adjuvant chemotherapy. This may lead to an improvement in outcomes for these subsets of patients.”

de Melo Gagliato D, Gonzalez-Angulo AM, Lei X, et al. Clinical impact of delaying initiation of adjuvant chemotherapy in patients with breast cancer [published online January 27, 2014]. J Clin Oncol. doi:10.1200/ JCO.2013.49.7693.

Related Videos
Julia Foldi, MD, PhD
Video 4 - "The Evolving Treatment Landscape with CDK4/6 Inhibitors in Early HR+/HER2- Breast Cancer"
Margaret E. Gatti-Mays, MD, MPH, FACP, of The Ohio State University Comprehensive Cancer Center
Ko Un “Clara” Park, MD
Erin Frances Cobain, MD
Video 3 - "5-Year Data from the MonarchE Trial Investigating Abemaciclib in HR+, HER2- High-Risk, Early Breast Cancer"
Rita Nanda, MD
Carlos Arteaga, MD
Video 2 - "NCCN Guidelines vs Real-World Practice: Risk Stratifying HR+/HER2- Early Breast Cancer"