Differential effect of body mass index (BMI) on outcomes of patients treated with docetaxel in prostate cancer - An exploratory analysis. (2022)
- Record Type:
- Journal Article
- Title:
- Differential effect of body mass index (BMI) on outcomes of patients treated with docetaxel in prostate cancer - An exploratory analysis. (2022)
- Main Title:
- Differential effect of body mass index (BMI) on outcomes of patients treated with docetaxel in prostate cancer - An exploratory analysis.
- Authors:
- Verma, Saurav
Arora, Shalabh
Sahoo, Ranjit Kumar
Singh, Prabhjot
Nayak, Brusabhanu
Haresh, KP
Das, Chandan J
Shamim, Shamim A
Kaushal, Seema
Batra, Atul - Abstract:
- Highlights: There is conflicting data on effect of docetaxel based on BMI in mCRPC patients. We analysed whether benefit of docetaxel in patients with mCRPC is modified by BMI. There was no effect of BMI on PFS in patients receiving docetaxel. Overweight and obese patients had a longer OS compared with lean patients. Abstract: Objective: : There are contradictory data on differential effect of docetaxel based on BMI in patients with breast and prostate cancer. We performed an exploratory analysis to determine if the benefit of docetaxel in patients with metastatic castration-resistant prostate cancer (mCRPC) is modified by BMI. Methods: : We performed a post ho c analysis of the data retrieved from the ENTHUSE M1C study. BMI (kg/m 2 ) was categorized as: 18.5 to <25 as lean; 25 to <30 as overweight; and ≥30 as obese. Cox regression models were constructed to determine the impact of BMI on progression-free survival (PFS) and overall survival (OS). Results: : A total of 466 patients were eligible for the current analysis. The median PFS was 7.3, 7.7 and 8.4 months (hazard ratio [HR], 0.92; 95% confidence interval [CI], 0.81 to 1.06; P = 0.261) in lean, overweight and obese patients. The median OS was 16.6, 20.1 and 21.4 months (HR, 0.75; 95% CI, 0.63 to 0.89; P = 0.002) for lean, overweight and obese patients. After adjusting for baseline and tumor characteristics, there was no association of BMI with PFS (overweight, HR, 0.89; 95% CI, 0.71 to 1.13; P = 0.353; obese, HR,Highlights: There is conflicting data on effect of docetaxel based on BMI in mCRPC patients. We analysed whether benefit of docetaxel in patients with mCRPC is modified by BMI. There was no effect of BMI on PFS in patients receiving docetaxel. Overweight and obese patients had a longer OS compared with lean patients. Abstract: Objective: : There are contradictory data on differential effect of docetaxel based on BMI in patients with breast and prostate cancer. We performed an exploratory analysis to determine if the benefit of docetaxel in patients with metastatic castration-resistant prostate cancer (mCRPC) is modified by BMI. Methods: : We performed a post ho c analysis of the data retrieved from the ENTHUSE M1C study. BMI (kg/m 2 ) was categorized as: 18.5 to <25 as lean; 25 to <30 as overweight; and ≥30 as obese. Cox regression models were constructed to determine the impact of BMI on progression-free survival (PFS) and overall survival (OS). Results: : A total of 466 patients were eligible for the current analysis. The median PFS was 7.3, 7.7 and 8.4 months (hazard ratio [HR], 0.92; 95% confidence interval [CI], 0.81 to 1.06; P = 0.261) in lean, overweight and obese patients. The median OS was 16.6, 20.1 and 21.4 months (HR, 0.75; 95% CI, 0.63 to 0.89; P = 0.002) for lean, overweight and obese patients. After adjusting for baseline and tumor characteristics, there was no association of BMI with PFS (overweight, HR, 0.89; 95% CI, 0.71 to 1.13; P = 0.353; obese, HR, 0.86; 95% CI, 0.66 to 1.13; P = 0.277) while overweight (HR, 0.68; 95% CI, 0.51 to 0.89; P = 0.006) and obese (HR, 0.59; 95% CI, 0.41 to 0.83; P = 0.003) patients had significantly better OS compared with lean patients. Conclusions: : There was no effect of BMI on PFS in patients with mCRPC receiving docetaxel. Interestingly, overweight and obese patients had a longer OS compared with lean patients, which is in contradiction to a recent study in breast cancer; and warrants further investigation. … (more)
- Is Part Of:
- Cancer treatment and research communications. Number 31(2022)
- Journal:
- Cancer treatment and research communications
- Issue:
- Number 31(2022)
- Issue Display:
- Volume 31, Issue 31 (2022)
- Year:
- 2022
- Volume:
- 31
- Issue:
- 31
- Issue Sort Value:
- 2022-0031-0031-0000
- Page Start:
- Page End:
- Publication Date:
- 2022
- Journal URLs:
- http://www.sciencedirect.com/ ↗
- DOI:
- 10.1016/j.ctarc.2022.100520 ↗
- Languages:
- English
- ISSNs:
- 2468-2942
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21546.xml