Weill Cornell Medical College in Qatar, Doha, Qatar
Reem Chamseddine , Stella Major , Arash Rafii , Hind Doha Elmalik
Background: Body Mass Index (BMI) is a significant prognostic factor in the survival of patients with hormone receptor-positive breast cancer (BC).[1-2] However, the relationship between BMI and survival is not well-established in hormone receptor-negative (HR-) breast tumors. [3] Emerging data is mixed: some studies show that BMI does not impact outcomes in HR- tumors [4], while others reveal worse survival in patients with elevated BMI.[5] In this study, our objective was to corroborate recent evidence about the relationship between BMI and mortality in hormone-negative breast cancer. Methods: We used the PLCO cancer screening trial, a publicly available database containing information about 155,000 participants enrolled in the United States between 1993 and 2001. Data were collected on cancer mortality through 2018 (median follow-up of 19.2 years post enrollment). The methodology of the PLCO trial has been described previously.[6] All female patients with a diagnosis of HR- BC diagnoses were selected for data retrieval, including HR-/HER2+ and HR-/HER2- tumors. Patients with equivocal receptor status were excluded. We used multivariate Cox regression to analyze mortality by BMI category, after adjusting for all significant variables at the bivariate level (p<0.25). Results: 348 women with confirmed HR- BC at the time of study participation were included. Mean age was 69 years old, and 62 patients (17.8%) passed away due to breast cancer during study enrollment or follow-up. Patients who were of normal weight (BMI 25-<30) at age of trial enrollment were not significantly more likely to survive compared to overweight or obese patients (Hazard Ratio 1.274, p= 0.623). Conclusions: Our results show no significant relationship between BMI and mortality in patients with HR- BC tumors. This finding adds to the growing literature about weight status in hormone receptor-negative tumors. Our data suggests that the mechanism of tumor progression in HR- breast tumors is unlikely to involve signaling mechanisms in adipocytes. Clinical trial information: NCT00002540, NCT01696968, NCT01696981, NCT01696994.
Baseline Characteristics | P value for bivariate Cox regression | Hazard ratio (95% CI) * | P value for multivariate Cox regression |
---|---|---|---|
Age at diagnosis | 0.578 | - | - |
Race | 0.297 | - | - |
Number of comorbidities | 0.134 Diabetes:0.023 | - | 0.811 Diabetes: 0.034 |
Tumor Histology | 0.172 | - | 0.405 |
Stage | <0.001 | - | <0.001 |
HER2 Status | 0.400 | - | - |
Underweight Category ** (BMI < 18.5) | - | 2.598 (0.220-30.645) | 0.448 |
Normal Weight Category (BMI 18.5 - < 25) | - | 1.274 (0.485-3.342) | 0.623 |
Overweight Category (BMI 25 - < 30) | - | 0.456 (0.199-1.046) | 0.064 |
* Values are hazard ratios (HR) relative to the reference (obese category, BMI ³30). HRs were adjusted for history of diabetes and tumor stage, factors significant at p<0.25 at the bivariate level. ** Cell number < 5.
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