The DASciS Software for BSI Calculation as a Valuable Prognostic Tool in mCRPC Treated with 223RaCl2: A Multicenter Italian Study

Author:

De Feo Maria Silvia1,Frantellizzi Viviana1ORCID,Bauckneht Matteo23ORCID,Farcomeni Alessio4ORCID,Filippi Luca5ORCID,Rizzini Elisa Lodi6ORCID,Lavelli Valentina7,Stazza Maria Lina8,Di Raimondo Tania2,Fornarini Giuseppe9ORCID,Rebuzzi Sara Elena1011ORCID,Filippo Mammini612,Mammucci Paolo7,Marongiu Andrea8ORCID,Monari Fabio612,Rubini Giuseppe7ORCID,Spanu Angela8ORCID,De Vincentis Giuseppe1ORCID

Affiliation:

1. Department of Radiological Sciences, Oncology and Anatomo-Pathology, Sapienza, University of Rome, 00161 Rome, Italy

2. Department of Health Sciences (DISSAL), University of Genova, 16132 Genova, Italy

3. Nuclear Medicine, IRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy

4. Department of Economics & Finance, University of Rome “Tor Vergata”, 00133 Rome, Italy

5. Department of Nuclear Medicine, Santa Maria Goretti Hospital, 04100 Latina, Italy

6. Radiation Oncology, IRCSS Azienza Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy

7. Nuclear Medicine Section, Interdisciplinary Department of Medicine, University of Bari “Aldo Moro”, 70124 Bari, Italy

8. Unit of Nuclear Medicine, Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy

9. Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy

10. Medical Oncology, Ospedale San Paolo, 17100 Savona, Italy

11. Department of Internal Medicine and Medical Specialties (Di.M.I.), University of Genova, 16132 Genova, Italy

12. Radiation Oncology, Department of Medical and Surgical Siences (DIMEC), Alma Mater Studiorum Bologna University, 40138 Bologna, Italy

Abstract

Background/Aim: Radium-223 dichloride (223RaCl2) represents a therapeutic option for metastatic castration-resistant prostate cancer (mCRPC) patients dealing with symptomatic bone metastases. The identification of baseline variables potentially affecting the life-prolonging role of 223RaCl2 is still ongoing. Bone scan index (BSI) defines the total load of bone metastatic disease detected on a bone scan (BS) and is expressed as a percentage value of the whole bone mass. The aim of this multicenter study was to assess the impact of baseline BSI on overall survival (OS) in mCRPC patients treated with 223RaCl2. For this purpose, the DASciS software developed by the Sapienza University of Rome for BSI calculation was shared between six Italian Nuclear Medicine Units. Methods: 370 pre-treatment BS were analyzed through the DASciS software. Other clinical variables relevant to OS analysis were taken into account for the statistical analysis. Results: Of a total of 370 patients, 326 subjects had died at the time of our retrospective analysis. The median OS time from the first cycle of 223RaCl2 to the date of death from any cause or last contact was 13 months (95%CI 12–14 months). The mean BSI value resulted in 2.98% ± 2.42. The center-adjusted univariate analysis showed that baseline BSI was significantly associated with OS as an independent risk factor (HR 1.137, 95%CI: 1.052–1.230, p = 0.001), meaning that patients with higher BSI values had worse OS. When adjusting for other measures on multivariate analysis, in addition to Gleason score and baseline values of Hb, tALP, and PSA, baseline BSI was confirmed to be a statistically significant parameter (HR 1.054, 95%CI: 1.040–1.068, p < 0.001). Conclusions: Baseline BSI significantly predicts OS in mCRPC treated with 223RaCl2. The DASciS software was revealed to be a valuable tool for BSI calculation, showing rapid processing time and requiring no more than a single demonstrative training for each participating center.

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference51 articles.

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