PRO-BMI study: prognostic role of body mass index (BMI) in metastatic castration resistant prostate cancer (mCRPC) patients receiving chemotherapy.

Authors

null

Marcello Tucci

San Luigi Hospital, Orbassano (Turin), Italy

Marcello Tucci , Stefania Eufemia Lutrino , Massimo Di Maio , Giuseppe Procopio , Francesco Massari , Nicola Calvani , Caterina Fontanella , Francesco Atzori , Sandro Barni , Chiara Caliolo , Francesca Vignani , Caterina Accettura , Annamaria Quaranta , Enrica Mazzoni , Maria D'amico , Claudio Scavelli , Maria Concetta Chetrì , Pasqualinda Ferrara , Saverio Cinieri

Organizations

San Luigi Hospital, Orbassano (Turin), Italy, Perrino Hospital, Brindisi, Italy, Department of Oncology, University of Turin, Orbassano (TO), Italy, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy, Medical Oncology, Azienda Ospedaliera Universitaria Integrata, University of Verona, Verona, Italy, Oncology Department A Perrino Hospital, Brindisi, Italy, University Hospital, Udine, Italy, Struttura Complessa di Oncologia Medica, A.O.U. di Cagliari, Cagliari, Italy, Division of Oncology, Azienda Ospedaliera Treviglio, Treviglio, Italy, Medical Oncology & Breast Unit, Brindisi, Italy, Department of Oncology, AOU San Luigi Gonzaga, Orbassano (TO), Italy, Medical Oncology, V. Fazzi- Lecce, Lecce, Italy, Medical Oncology & Breast Unit, A. Perrino Hospital, Brindisi, Italy, Medical Oncology Unit and Breast Unit, S Perrino Hospital, Brindisi, Italy, Gallipoli S. Cuore Hospital, Gallipoli, Italy, Medical Oncology & Breast Unit,, Brindisi, Italy, Sen Antonio Perrino Hospital, Francavilla Fontana, Italy

Research Funding

Other

Background: Limited data are available regarding the relationship between body mass index (BMI) and metastatic castration resistant prostate cancer (mCRPC). Pro-BMI trial is an Italian, observational, retrospective study designed to evaluate the correlation between BMI and outcome, in terms of progression-free survival (PFS) and overall survival (OS), of mCRPC patients (pts) treated with first-line chemotherapy. Methods: We analyzed 212 consecutive mCRPC pts who received docetaxel 75 mg/m2 every 3 weeks as first-line therapy in 10 Italian Institutions between 2003 and 2015. Data about baseline characteristics, treatment and outcome were collected in an anonymized dedicated database. Pts were stratified in 3 groups according to the World Health Organization BMI classification: normal weight (BMI < 25kg/m2), overweight (25 ≤ BMI < 30kg/m2), and obese (BMI ≥ 30kg/m2). PFS and OS were measured from the date of start of docetaxel: preplanned analyses aimed to compare obese vs. normal/overweight pts. Results: The median age at the time of start of docetaxel for mCRPC was 69 years (range 45-87). At baseline, 32% of pts were normal weight, 51% were overweight, and 17% were obese. 89% of obese pts had at least 1 co-morbidity versus 63% of overweight pts and 54% of normal weight pts (p = 0.002). PFS was not statistically different between obese (median 10.4 months) and normal/overweight pts (median 7.2 months, Hazard Ratio 0.84, 95%CI 0.58 – 1.22, p = 0.35). Similarly, OS was not statistically different between obese (median 27.7 months) and normal/overweight pts (median 24.4 months, Hazard Ratio 0.80, 95%CI 0.49 – 1.31, p = 0.38). Proportion of pts starting with full dose and needing dose reduction was slightly higher in obese pts (32.4%) vs. normal/overweight pts (21.5%), but this difference was not statistically significant (p = 0.17). Incidence of any hematologic toxicity was significantly higher in obese pts (69% vs 50%, p = 0.03). Conclusions: In this retrospective analysis, no significant association between BMI and outcome of pts receiving docetaxel for mCRPC was found. However, our results suggest that obesity could be associated with a lower tolerance to chemotherapy.

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Abstract Details

Meeting

2016 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Genitourinary (Prostate) Cancer

Track

Genitourinary Cancer—Prostate, Testicular, and Penile

Sub Track

Prostate Cancer - Advanced Disease

Citation

J Clin Oncol 34, 2016 (suppl; abstr e16543)

DOI

10.1200/JCO.2016.34.15_suppl.e16543

Abstract #

e16543

Abstract Disclosures