Development of a predictive model for patients with bone metastases referred to palliative radiotherapy: Secondary analysis of a multicenter study (the PRAIS trial)

被引:0
作者
Rossi, Romina [1 ,2 ]
Medici, Federica [2 ,3 ]
Habberstad, Ragnhild [4 ,5 ]
Klepstad, Pal [6 ,7 ]
Cilla, Savino [8 ]
Dall'Agata, Monia [9 ]
Kaasa, Stein [10 ]
Caraceni, Augusto Tommaso [11 ,12 ]
Morganti, Alessio Giuseppe [2 ,3 ]
Maltoni, Marco [13 ]
机构
[1] IRCCS, Ist Romagnolo Studio Tumori IRST Dino Amadori, I-47014 Meldola, Italy
[2] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci DIMEC, Radiat Oncol, Bologna, Italy
[3] IRCCS Azienda Osped Univ Bologna, Radiat Oncol, Via Albertoni 15, I-40138 Bologna, Italy
[4] Norwegian Univ Sci & Technol, Dept Clin & Mol Med, Trondheim, Norway
[5] St Olavs Univ Hosp, Dept Oncol, Trondheim, Norway
[6] Norwegian Univ Sci & Technol, Dept Circulat & Med Imaging, Trondheim, Norway
[7] St Olavs Univ Hosp, Dept Anesthesiol & Intens Care Med, Trondheim, Norway
[8] Responsible Res Hosp, Med Phys Unit, Campobasso, Italy
[9] IRCCS, Ist Romagnolo Studio Tumori IRST Dino Amadori, Unit Biostat & Clin Trials, Meldola, Italy
[10] Oslo Univ Hosp, Dept Oncol, Oslo, Norway
[11] Fdn IRCCS Ist Nazl Tumori, Palliat Care Pain Therapy & Rehabil Unit, Milan, Italy
[12] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
[13] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci DIMEC, Pharmacol Unit, Bologna, Italy
来源
CANCER MEDICINE | 2024年 / 13卷 / 19期
关键词
bone metastasis; LASSO; multicenter; palliative therapy; predictive model; radiotherapy; PROGNOSTIC-FACTORS; SCORING SYSTEM; TERMINALLY-ILL; IL-8; CANCER; SURVIVAL; INTERLEUKIN-8; INVASIVENESS; VEGF;
D O I
10.1002/cam4.70050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The decision to administer palliative radiotherapy (RT) to patients with bone metastases (BMs), as well as the selection of treatment protocols (dose, fractionation), requires an accurate assessment of survival expectancy. In this study, we aimed to develop three predictive models (PMs) to estimate short-, intermediate-, and long-term overall survival (OS) for patients in this clinical setting. Materials and Methods This study constitutes a sub-analysis of the PRAIS trial, a longitudinal observational study collecting data from patients referred to participating centers to receive palliative RT for cancer-induced bone pain. Our analysis encompassed 567 patients from the PRAIS trial database. The primary objectives were to ascertain the correlation between clinical and laboratory parameters with the OS rates at three distinct time points (short: 3 weeks; intermediate: 24 weeks; prolonged: 52 weeks) and to construct PMs for prognosis. We employed machine learning techniques, comprising the following steps: (i) identification of reliable prognostic variables and training; (ii) validation and testing of the model using the selected variables. The selection of variables was accomplished using the LASSO method (Least Absolute Shrinkage and Selection Operator). The model performance was assessed using receiver operator characteristic curves (ROC) and the area under the curve (AUC). Results Our analysis demonstrated a significant impact of clinical parameters (primary tumor site, presence of non-bone metastases, steroids and opioid intake, food intake, and body mass index) and laboratory parameters (interleukin 8 [IL-8], chloride levels, C-reactive protein, white blood cell count, and lymphocyte count) on OS. Notably, different factors were associated with the different times for OS with only IL-8 included both in the PMs for short- and long-term OS. The AUC values for ROC curves for 3-week, 24-week, and 52-week OS were 0.901, 0.767, and 0.806, respectively. Conclusions We successfully developed three PMs for OS based on easily accessible clinical and laboratory parameters for patients referred to palliative RT for painful BMs. While our findings are promising, it is important to recognize that this was an exploratory trial. The implementation of these tools into clinical practice warrants further investigation and confirmation through subsequent studies with separate databases.
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页数:12
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