Circulating SMRP and CA-125 before and after pleurectomy decortication for pleural mesothelioma

被引:1
作者
Paajanen, Juuso [1 ,2 ,3 ,7 ,8 ,9 ]
Sadek, Ahmed [1 ,2 ,3 ]
Richards, William G. [1 ,2 ,3 ]
Xie, Yue [4 ]
Mazzola, Emanuele [4 ]
Sidopoulos, Kristina [1 ,2 ,3 ]
Kuckelman, John [1 ,2 ,3 ]
Gill, Ritu R. [5 ,6 ]
Bueno, Raphael [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Thorac Surg Oncol Lab, Boston, MA USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Int Mesothelioma Program, Div Thorac Surg, Boston, MA USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Lung Ctr, Boston, MA USA
[4] Dana Farber Canc Inst, Deparment Data Sci, Boston, MA USA
[5] Beth Israel Deaconess Med Ctr, Dept Radiol, Boston, MA USA
[6] Harvard Med Sch, Boston, MA USA
[7] Brigham & Womens Hosp, Div Thorac Surg, 75 Francis St, Boston, MA 02115 USA
[8] Brigham & Womens Hosp, Lung Ctr, 75 Francis St, Boston, MA 02115 USA
[9] Harvard Med Sch, 75 Francis St, Boston, MA 02115 USA
关键词
biomarkers; CA-125; pleural mesothelioma; pleurectomy decortication; SMRP; PERITONEAL MESOTHELIOMA; MULTIMODALITY THERAPY; SERUM MESOTHELIN; TUMOR-MARKERS; CA125; OSTEOPONTIN; MANAGEMENT; DIAGNOSIS; PROGNOSIS; FIBULIN-3;
D O I
10.1111/1759-7714.15264
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Tumor recurrence remains the main barrier to survival after surgery for pleural mesothelioma (PM). Soluble mesothelin-related protein (SMRP) and cancer antigen 125 (CA-125) are established blood-based biomarkers for monitoring PM. We prospectively studied the utility of these biomarkers after pleurectomy decortication (PD). Methods: Patients who underwent PD and achieved complete macroscopic resection with available preoperative SMRP levels were included. Tumor marker levels were determined within 60 days of three timepoints: (1) preoperation, (2) post-operation, and (3) recurrence. Results: Of 356 evaluable patients, 276 (78%) had recurrence by the end of follow-up interval. Elevated preoperative SMRP levels were associated with epithelioid histology (p < 0.013), advanced TNM (p < 0.001) stage, and clinical stage (p < 0.001). Preoperative CA-125 levels were not significantly associated with clinical covariates. Neither biomarker was associated with survival or disease-free survival. With respect to nonpleural and nonlymphatic recurrences, mean SMRP levels were elevated in patients with pleural (p = 0.021) and lymph node (p = 0.042) recurrences. CA-125 levels were significantly higher in patients with abdominal (p < 0.001) and lymph node (p = 0.004) recurrences. Among patients with all three timepoints available, we observed an average decrease in SMRP levels by 1.93 nmol/L (p < 0.001) postoperatively and again an average increase at recurrence by 0.79 nmol/L (p < 0.001). There were no significant changes in levels of CA-125 across the study timepoints (p = 0.47). Conclusions: Longitudinal changes in SMRP levels corresponded with a radiographic presence of disease in a subset of patients. SMRP surveillance could aid in detection of local recurrences, whereas CA-125 could be helpful in recognizing abdominal recurrences.
引用
收藏
页码:1237 / 1245
页数:9
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