Supplementary Prognostic Variables for Pleural Mesothelioma A Report from the IASLC Staging Committee

被引:57
作者
Pass, Harvey I. [1 ]
Giroux, Dorothy [2 ]
Kennedy, Catherine [3 ]
Ruffini, Enrico [4 ]
Cangir, Ayten K. [5 ]
Rice, David [6 ]
Asamura, Hisao [7 ]
Waller, David [8 ]
Edwards, John [9 ]
Weder, Walter [10 ]
Hoffmann, Hans [11 ]
van Meerbeeck, Jan P. [12 ]
Rusch, Valerie W. [13 ]
机构
[1] NYU Langone Med Ctr, Dept Cardiothorac Surg, New York, NY 10016 USA
[2] Univ Washington, Dept Stat, Seattle, WA 98195 USA
[3] Univ Sydney, Strathfield Private Hosp Campus, Dept Cardiothorac Surg, Sydney, NSW 2006, Australia
[4] Univ Torino, Dept Thorac Surg, Osped San Giovanni Battista, Turin, Italy
[5] Ankara Univ Fac Med, Dept Thorac Surg, Ankara, Turkey
[6] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX 77030 USA
[7] Natl Canc Ctr, Tokyo, Japan
[8] Glenfield Gen Hosp, Dept Thorac Surg, Leicester LE3 9QP, Leics, England
[9] No Gen Hosp, Dept Cardiothorac Surg, Sheffield, S Yorkshire, England
[10] Univ Zurich Hosp, CH-8091 Zurich, Switzerland
[11] Heidelberg Univ, Dept Thorac Surg, Thoraxklin, Heidelberg, Germany
[12] Univ Hosp, Ghent, Belgium
[13] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10021 USA
关键词
Mesothelioma; Surgery; Prognosis; Registry; Staging; TO-LYMPHOCYTE RATIO; PHASE-II TRIALS; MALIGNANT MESOTHELIOMA; EXTRAPLEURAL PNEUMONECTOMY; INTERNATIONAL-ASSOCIATION; LUNG-CANCER; SURVIVAL; VALIDATION; EXPRESSION; VOLUME;
D O I
10.1097/JTO.0000000000000181
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The staging system for malignant pleural mesothelioma is controversial. To revise this system, the International Association for the Study of Lung Cancer Staging Committee developed an international database. This report analyzes prognostic variables in a surgical population, which are supplementary to previously published CORE variables (stage, histology, sex, age, and type of procedure). Methods: Supplementary prognostic variables were studied in three scenarios: (1) all data available, that is, patient pathologically staged and other CORE variables available (2) only clinical staging available along with CORE variables, and (3) only age, sex, histology, and laboratory parameters are known. Survival was analyzed by Kaplan-Meier, prognostic factors by log rank and stepwise Cox regression modeling after elimination of nonsignificant variables. p value less than 0.05 was significant. Results: A total of 2141 patients with best tumor, node, metastasis (TNM) stages (pathologic with/without clinical staging) had nonmissing age, sex, histology, and type of surgical procedure. Three prognostic models were defined. Scenario A (all parameters): best pathologic stage, histology, sex, age, type of surgery, adjuvant treatment, white blood cell count (WBC) (>= 15.5 or not), and platelets (>= 400 k or not) (n = 550). Scenario B (no surgical staging): clinical stage, histology, sex, age, type of surgery, adjuvant treatment, WBC, hemoglobin (<14.6 or not), and platelets (n = 627). Scenario C (limited data): histology, sex, age, WBC, hemoglobin, and platelets (n = 906). Conclusion: Refinement of these models could define not only the appropriate patient preoperatively for best outcomes after cytoreductive surgery but also stratify surgically treated patients after clinical and pathologic staging who do or do not receive adjuvant therapy.
引用
收藏
页码:856 / 864
页数:9
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