scholarly journals EP-1402: Impact of SBRT on pain and local control for bone metastases: a systematic review and meta-analysis

2017 ◽  
Vol 123 ◽  
pp. S749
Author(s):  
J.M. Van der Velden ◽  
A.S. Gerlich ◽  
E. Wong ◽  
E. Chow ◽  
M. Intven ◽  
...  
2019 ◽  
Vol 111 (10) ◽  
pp. 1023-1032 ◽  
Author(s):  
Katie L Spencer ◽  
Joanne M van der Velden ◽  
Erin Wong ◽  
Enrica Seravalli ◽  
Arjun Sahgal ◽  
...  

Abstract Background Stereotactic radiotherapy (SBRT) might improve pain and local control in patients with bone metastases compared to conventional radiotherapy, although an overall estimate of these outcomes is currently unknown. Methods A systematic review was carried out following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Pubmed, Embase, and Cochrane databases were systematically searched to identify studies reporting pain response and local control among patients with bone metastases from solid-organ tumors who underwent SBRT in 1–6 fractions. All studies prior to April 15, 2017, were included. Study quality was assessed by predefined criteria, and pain response and local control rates were extracted. Results A total of 2619 studies were screened; 57 were included (reporting outcomes for 3995 patients) of which 38 reported pain response and 45 local control rates. Local control rates were high with pain response rates above those previously reported for conventional radiotherapy. Marked heterogeneity in study populations and delivered treatments were identified such that quantitative synthesis was not appropriate. Reported toxicity was limited. Of the pain response studies, 73.7% used a retrospective cohort design and only 10.5% used the international consensus endpoint definitions of pain response. The median survival within the included studies ranged from 8 to 30.4 months, suggesting a high risk of selection bias in the included observational studies. Conclusions This review demonstrates the potential benefit of SBRT over conventional palliative radiotherapy in improving pain due to bone metastases. Given the methodological limitations of the published literature, however, large randomized trials are now urgently required to better quantify this benefit.


2017 ◽  
Vol 115 ◽  
pp. 67-80 ◽  
Author(s):  
Jean-Jacques Body ◽  
Geoffrey Quinn ◽  
Susan Talbot ◽  
Emma Booth ◽  
Gaston Demonty ◽  
...  

2019 ◽  
Vol 176 (3) ◽  
pp. 507-517 ◽  
Author(s):  
Arif Ali Awan ◽  
Brian Hutton ◽  
John Hilton ◽  
Sasha Mazzarello ◽  
Catherine Van Poznak ◽  
...  

2015 ◽  
Vol 26 (11) ◽  
pp. 2205-2213 ◽  
Author(s):  
M.F.K. Ibrahim ◽  
S. Mazzarello ◽  
R. Shorr ◽  
L. Vandermeer ◽  
C. Jacobs ◽  
...  

2013 ◽  
Vol 49 (2) ◽  
pp. 416-430 ◽  
Author(s):  
John A. Ford ◽  
Rob Jones ◽  
Andrew Elders ◽  
Clive Mulatero ◽  
Pamela Royle ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e16067-e16067
Author(s):  
Kenji Omae ◽  
Yasushi Tsujimoto ◽  
Michitaka Honda ◽  
Tsunenori Kondo ◽  
Yasunobu Hashimoto ◽  
...  

e16067 Background: Bone-modifying agents (BMA) have been well-demonstrated to be effective for preventing and inhibiting skeletal-related events (SRE) in patients with bone metastases of breast or prostate cancer. However, the role of BMA treatment has not yet been clearly defined in patients with bone metastases of renal cell carcinoma (RCC). We, therefore, conducted a systematic review and meta-analysis to evaluate the efficacy and safety of BMA in patients with bone metastases of RCC. Methods: Literature search was conducted on MEDLINE, the Cochrane Central Register of Controlled Trials, the WHO International Clinical Trials Registry Platform, and ClinicalTrials.gov to identify randomized controlled trials of BMA for the treatment of bone metastases in RCC patients. The primary outcomes were SRE and serious adverse events (AEs). Hazard ratios (HRs) were calculated with a random effects model. The Grading of Recommendation Assessment, Development, and Evaluation (GRADE) approach was used to assess the certainty of the evidence. This review was prospectively registered on PROSPERO (No. CRD42016032742). Results: Three studies (259 patients) were identified for the systematic review. Two studies that compared zoledronic acid with placebo or non-zoledronic acid showed that zoledronic acid reduced the SRE risk by 68% (HR 0.32; 95% confidence interval (CI) 0.19–0.55; P < 0.0001). The quality of evidence was moderate. No serious osteonecrosis was reported in both studies. The incidence of serious AEs was identical (80%) on both treatment arms in one study and not reported in the other study. In the remaining study, which compared denosumab with zoledronic acid, analyses of the individual patient data shared through Amgen showed a favorable trend for denosumab in terms of SRE (HR 0.71; 95% CI 0.43–1.17) and serious AEs (risk ratio 0.86; 95% CI 0.68–1.08), but this trend did not reach statistical significance. Conclusions: The moderate-quality evidence indicates that zoledronic acid significantly reduces the risk of SRE among patients with bone metastases of RCC.


2021 ◽  
Vol 94 ◽  
pp. 102168
Author(s):  
Esmeralda Garcia-Torralba ◽  
Francesca Spada ◽  
Kok Haw Jonathan Lim ◽  
Timothy Jacobs ◽  
Jorge Barriuso ◽  
...  

Rare Tumors ◽  
2013 ◽  
Vol 5 (1) ◽  
pp. 5-10 ◽  
Author(s):  
Thomas J. Wood ◽  
Kathleen M. Quinn ◽  
Forough Farrokhyar ◽  
Ben Deheshi ◽  
Tom Corbett ◽  
...  

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