Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set
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作者:
Fibla, Juan J.
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Mayo Clin, Div Gen Thorac Surg, Rochester, MN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Fibla, Juan J.
[1
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Cassivi, Stephen D.
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Mayo Clin, Div Gen Thorac Surg, Rochester, MN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Cassivi, Stephen D.
[1
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Brunelli, Alessandro
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Mayo Clin, Div Gen Thorac Surg, Rochester, MN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Brunelli, Alessandro
[1
]
Decker, Paul A.
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Mayo Clin, Div Biostat, Rochester, MN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Decker, Paul A.
[2
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Allen, Mark S.
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Mayo Clin, Div Gen Thorac Surg, Rochester, MN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Allen, Mark S.
[1
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Darling, Gail E.
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Univ Toronto, Div Thorac Surg, Toronto, ON, CanadaMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Darling, Gail E.
[3
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Landreneau, Rodney J.
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Univ Pittsburgh, Med Ctr, Dept Surg, Pittsburgh, PA USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Landreneau, Rodney J.
[4
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Putnam, Joe B.
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Vanderbilt Univ, Div Thorac Surg, Memphis, TN USAMayo Clin, Div Gen Thorac Surg, Rochester, MN USA
Putnam, Joe B.
[5
]
机构:
[1] Mayo Clin, Div Gen Thorac Surg, Rochester, MN USA
[2] Mayo Clin, Div Biostat, Rochester, MN USA
[3] Univ Toronto, Div Thorac Surg, Toronto, ON, Canada
[4] Univ Pittsburgh, Med Ctr, Dept Surg, Pittsburgh, PA USA
[5] Vanderbilt Univ, Div Thorac Surg, Memphis, TN USA
Purpose: This study seeks to clarify the modern prognostic significance of visceral pleura invasion (VPI) in Stage IB (T2aN0M0) non-small cell lung cancer (NSCLC) within the context of the 7th edition TNM classification using the data set from a recent prospective multicenter trial. Patients and methods: 1111 early-stage NSCLC patients participating in the ACOSOG Z0030 trial (1990-2004) underwent curative pulmonary resection. After excluding T2b tumours (>5 cm and <= 7 cm) and non-size-based T2 factors other than VPI, 289 patients were categorized as Stage IB NSCLC - T2aN0M0 - according to the AJCC 7th edition classification. The patients were divided into three groups according to size and VPI: tumours <= 3 cm with VPI (Group I, "VPI-alone", n = 83), tumours > 3 cm and <= 5 cm without VPI (Group II, "Size-alone", n = 156), and turnouts > 3 cm and <= 5 cm with VPI (Group III, "VPI +Size", n = 50). Multivariate Cox regression analysis was used to assess the association of VPI and size with survival, adjusting for age, gender, histology and type of resection. Results: VPI in Stage IB was identified in 133 patients (46.0%). Survival analysis in these patients identified an optimal cutpoint for survival based on size of 3.1 cm. Group III (VPI + Size) had a 5-year survival rate of 55.0% significantly shorter when compared to Group I (VPI-alone = 68.3%, p = 0.009), and Group II (Size-alone = 67.2%, p = 0.021). No difference was found between Groups land II. Multivariable analysis showed that VPI associated with size was an independent negative prognostic factor of long-term survival, along with older age and limited resection. Conclusions: Stage IB patients with VPI and tumours >3 cm and <= 5 cm have significantly worse prognosis than those with 'T2a' tumours on the basis of VPI or tumour size alone. This finding would suggest upstaging these patients from the current IB status to Stage IIA. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
机构:
Univ Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Ignatius, Sai-Hong
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Zell, Jason A.
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Univ Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Zell, Jason A.
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Ziogas, Argyrios
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Univ Calif Irvine, Genet Epidemiol Res Inst, Irvine, CA USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Ziogas, Argyrios
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Anton-Culver, Hoda
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Univ Calif Irvine, Genet Epidemiol Res Inst, Irvine, CA USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
机构:
Univ Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Ignatius, Sai-Hong
;
Zell, Jason A.
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机构:
Univ Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Zell, Jason A.
;
Ziogas, Argyrios
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机构:
Univ Calif Irvine, Genet Epidemiol Res Inst, Irvine, CA USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA
Ziogas, Argyrios
;
Anton-Culver, Hoda
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif Irvine, Genet Epidemiol Res Inst, Irvine, CA USAUniv Calif Irvine, Med Ctr, Chao Family Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Orange, CA 92868 USA