Complete pathological response is predictive for clinical outcome after tri-modality therapy for carcinomas of the superior pulmonary sulcus

被引:19
作者
Blaauwgeers, Johannes L. [1 ]
Kappers, Ingrid [2 ]
Klomp, Houke M. [2 ]
Belderbos, Jose S. [3 ]
Dijksman, Lea M. [4 ]
Smit, Egbert F. [5 ]
Postmus, Pieter E. [5 ]
Paul, Marinus A. [6 ]
Oosterhuis, Jan W. [6 ]
Hartemink, Koen J. [6 ]
Vos, Cornelis G. [6 ]
Burgers, Jacobus A. [7 ]
Dahele, Max [8 ]
Phernambucq, Erik C. [8 ]
Witte, Birgit I. [9 ]
Thunnissen, Erik [10 ]
机构
[1] Onze Lieve Vrouw Hosp, Dept Pathol, NL-1090 HM Amsterdam, Netherlands
[2] Netherlands Canc Inst NKI AVL, Dept Surg, Amsterdam, Netherlands
[3] Netherlands Canc Inst NKI AVL, Dept Radiotherapy, Amsterdam, Netherlands
[4] Onze Lieve Vrouw Hosp, Dept Teaching Hosp, NL-1090 HM Amsterdam, Netherlands
[5] VU Univ Med Ctr VUmc, Dept Pulmonol, Amsterdam, Netherlands
[6] VU Univ Med Ctr VUmc, Dept Surg, Amsterdam, Netherlands
[7] Netherlands Canc Inst NKI AVL, Dept Pulmonol, Amsterdam, Netherlands
[8] VU Univ Med Ctr VUmc, Dept Radiat Oncol, Amsterdam, Netherlands
[9] VU Univ Med Ctr VUmc, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[10] VU Univ Med Ctr VUmc, Dept Pathol, Amsterdam, Netherlands
关键词
Pancoast; Lung cancer; Chemoradiation; Histopathology; Prognosis; INDUCTION CHEMORADIATION; NEOADJUVANT THERAPY; SURGICAL RESECTION; CANCER; REGRESSION; RADIATION;
D O I
10.1007/s00428-013-1404-6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The objective was to define the relationship between histopathological changes after pre-operative chemo-radiotherapy (CRT) and clinical outcome following tri-modality therapy in patients with superior sulcus tumours. A retrospective analysis of tumour material was performed in a series of 46 patients who received tri-modality therapy between 1997 and 2007. Median follow-up was 34 months (5-154). Pathological complete response (pCR) was present in 20/46 tumours (43 %). The most common RECIST score after CRT in patients with pCR was a partial response (PR; 10/17, three unknown), whereas in patients without a pCR, stable disease was the most common (22/26) (p = 0.002). In 26 specimens with residual tumour, this was mainly located in the periphery of the lesion rather than the centre (Spearman's correlation = 0.67, p < 0.001). Prognosis was significantly better after a pCR compared to residual tumour (70 % 5-year overall survival vs. 20 %; p = 0.001) and in patients with fewer than 10 % vital tumour cells as compared to those with > 10 % (65 % 5-year overall survival vs. 18 %; p < 0.001). A low mitotic count was associated with a longer disease-free survival (p = 0.02). Complete pathological response and the presence of fewer than 10 % vital tumour cells after pre-operative CRT are both associated with a more favourable prognosis. A modification of the pathological staging system after radiotherapy, incorporating the percentage of vital tumour cells, is proposed.
引用
收藏
页码:547 / 556
页数:10
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