Micropapillary and/or Solid Histologic Subtype Based on Pre-Treatment Biopsy Predicts Local Recurrence After Thermal Ablation of Lung Adenocarcinoma

被引:22
作者
Gao, Song [1 ,2 ]
Stein, Seth [1 ]
Petre, Elena N. [1 ]
Shady, Waleed [1 ]
Durack, Jeremy C. [1 ]
Ridge, Carole [1 ,3 ]
Adusumilli, Prasad [4 ]
Rekhtman, Natasha [5 ]
Solomon, Stephen B. [1 ]
Ziv, Etay [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Intervent Radiol Serv, Howard 118,1275 York Ave, New York, NY 10065 USA
[2] Peking Univ, Canc Hosp & Inst, Key Lab Carcinogenesis & Translat Res, Intervent Therapy Dept,Minist Educ Beijing, Beijing 100142, Peoples R China
[3] Mater Misericordiae Univ Hosp, Dept Radiol, Dublin 7, Ireland
[4] Mem Sloan Kettering Canc Ctr, Thorac Surg Serv, Howard 118,1275 York Ave, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Pathol Diagnost Serv, Howard 118,1275 York Ave, New York, NY 10065 USA
关键词
Lung ablation; Histologic subtype; Micropapillary and solid; Local recurrence; RADIOFREQUENCY ABLATION; PERCUTANEOUS RADIOFREQUENCY; INTERNATIONAL ASSOCIATION; REPORTING CRITERIA; FOLLOW-UP; HIGH-RISK; CANCER; STANDARDIZATION; CLASSIFICATION; TERMINOLOGY;
D O I
10.1007/s00270-017-1760-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate whether histologic subtyping from biopsies can predict local recurrence after thermal ablation for lung adenocarcinoma. Patients treated with CT-guided thermal ablation for lung adenocarcinoma that had pre-ablation needle biopsy with analysis of histologic components were identified. Age, gender, smoking status, treatment indication (primary stage 1 tumor versus salvage), histologic subtype, ground-glass radiographic appearance, tumor size, ablation modality, and ablation margin were evaluated in relation to time to local recurrence (TTLR). Cumulative incidence of recurrence (CIR) was calculated using competing risks analysis and compared across groups using Fine and Grey method with clustering. Multivariate analysis was conducted with stepwise regression. There were 53 patients with 57 tumors diagnosed as adenocarcinoma on pre-ablation biopsy and with histologic subtype analysis. Of these, 19% (11) had micropapillary components, 14% (8) had solid components, and 26% (15) had micropapillary and/or solid components. In the univariate analysis, solid (subdistribution hazard ratio [SHR] = 4.04, p = 0.0051, 95% confidence interval [CI] = 1.52-10.7), micropapillary (SHR = 3.36, p = 0.01, CI = 1.33-8.47), and micropapillary and/or solid components (SHR = 5.85, p = 0.00038, CI = 2.21-15.5) were significantly correlated with shorter TTLR. On multivariate analysis, the presence of micropapillary and/or solid component (SHR = 11.4, p = 0.00021, CI: 3.14-41.3) was the only independent predictor of TTLR. The 1-, 2-, and 3-year CIR in patients with micropapillary and/or solid components was 33, 49, and 66% compared to 5, 14, and 18% in patients with no micropapillary or solid components on biopsy specimens. Micropapillary and/or solid histologic components identified in pre-ablation biopsy are associated with shorter TTLR after thermal ablation of lung adenocarcinoma.
引用
收藏
页码:253 / 259
页数:7
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