Abstract
Objective: We assessed the prognostic value of quantitative indices extracted from bone SPECT-CT to evaluate the response of bone metastatic castrate-resistant prostate cancer (BmCRPC) to abiraterone.Methods: Consecutive patients with BmCRPC initiating treatment with abiraterone from March 2014 to March 2015 were prospectively included. Three 2-bed SPECT-CT [at baseline [M0], after 3 months [M3], and 6 months [M6] of treatment], were planned (Symbia Intevo®, Siemens). SPECT data were reconstructed using an Ordered Subset Conjugate Gradient Minimization (OSCGM) algorithm allowing SUV quantification. SUVmax and SUVpeak of the highest uptake lesion were measured in each SPECT-CT. Total Neoplastic Osteoblastic Metabolic Volume (NOMV) was assessed. PSA level was recorded at baseline, M3, and M6 of treatment. Overall survival (OS), progression-free survival (PFS), and disease-specific survival (DSS) were calculated.Results: Nineteen patients aged 71.1 ± 7.7 years were included. Low M0 SUVmax was significantly predictive of longer OS (p = 0.04). Low NOMV at M0 were significantly predictive of longer PFS (p = 0.02). Patients with increase of at least 12.5% of the SUVpeak of the highest uptake lesion between M0 and M3 (ΔSUVpeakM0M3) had a significantly longer OS (p = 0.03). Patients with increase (or decrease lesser than 25%) of ΔSUVpeakM0M3 had a significantly longer DSS (p = 0.01). Patients with increase of NOMV of at least 45% between M0 and M6 had a significantly shorter PFS (p < 0.001). Variations of NOMV between M0 and M6 were significantly correlated with PSA variations between M0 and M6 (rs = 0.73, p = 0.02).Conclusions: Quantitative bone SPECT-CT appears to be a promising tool of BmCRPC assessment. Early flare-up phenomenon seems to predict longer OS.
Highlights
Prostate adenocarcinoma is one of the most common cancers in men [1], and bone remains the most frequent site of distant metastasis
Low M0 SUVmax was significantly predictive of longer overall survival (OS) (p = 0.04)
Low Neoplastic Osteoblastic Metabolic Volume (NOMV) at M0 were significantly predictive of longer progression-free survival (PFS) (p = 0.02)
Summary
Prostate adenocarcinoma is one of the most common cancers in men [1], and bone remains the most frequent site of distant metastasis. During the last two decades, the prostate cancer specific mortality has greatly decreased thanks to new therapeutic molecules, among which the second generation of hormonotherapy has revolutionized the treatment of metastatic castrate-resistant prostate cancer (mCRPC). The response assessment to this new generation hormone therapy and the identification of treatment-refractory patients remains a real challenge [4]. In 2007, the Prostate Cancer Working Group (PCWG) published the PCWG 2 criteria guiding the therapeutic response assessment in prostate cancer trials [5]. These criteria are based on composite data including clinical signs (such as general condition and bone pain), Prostatic Specific Antigen (PSA) variations, computed tomography (CT) scan [using RECIST 1.1 criteria [6]] and bone scan results
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