Validation of a Proposed Tumor Regression Grading Scheme for Pancreatic Ductal Adenocarcinoma After Neoadjuvant Therapy as a Prognostic Indicator for Survival

被引:92
作者
Lee, Sun Mi [1 ]
Katz, Matthew H. G. [2 ]
Liu, Li [1 ]
Sundar, Manonmani [4 ]
Wang, Hua [3 ]
Varadhachary, Gauri R. [3 ]
Wolff, Robert A. [3 ]
Lee, Jeffrey E. [2 ]
Maitra, Anirban [1 ,4 ]
Fleming, Jason B. [2 ]
Rashid, Asif [1 ]
Wang, Huamin [1 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Unit 085,1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Translat Mol Pathol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
pancreatic cancer; histologic tumor regression grade; neoadjuvant therapy; survival; prognosis; RANDOMIZED CONTROLLED-TRIAL; GEMCITABINE-BASED CHEMORADIATION; PREOPERATIVE CHEMORADIATION; RESECTABLE ADENOCARCINOMA; ADJUVANT CHEMOTHERAPY; CANCER; RESECTION; CARCINOMA; HEAD; CHEMORADIOTHERAPY;
D O I
10.1097/PAS.0000000000000738
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Neoadjuvant therapy has been increasingly used to treat patients with potentially resectable pancreatic ductal adenocarcinoma (PDAC). Although the College of American Pathologists (CAP) grading scheme for tumor response in posttherapy specimens has been used, its clinical significance has not been validated. Previously, we proposed a 3-tier histologic tumor regression grading (HTRG) scheme (HTRG 0, no viable tumor; HTRG 1, < 5% viable tumor cells; HTRG 2, >= 5% viable tumor cells) and showed that the 3-tier HTRG scheme correlated with prognosis. In this study, we sought to validate our proposed HTRG scheme in a new cohort of 167 consecutive PDAC patients who completed neoadjuvant therapy and pancreaticoduodenectomy. We found that patients with HTRG 0 or 1 were associated with a lower frequency of lymph node metastasis (P = 0.004) and recurrence (P = 0.01), lower ypT (P < 0.001) and AJCC stage (P < 0.001), longer disease-free survival (DFS, P = 0.004) and overall survival (OS, P = 0.02) than those with HTRG 2. However, there was no difference in either DFS or OS between the groups with CAP grade 2 and those with CAP grade 3 (P > 0.05). In multivariate analysis, HTRG grade 0 or 1 was an independent prognostic factor for better DFS (P = 0.03), but not OS. Therefore we validated the proposed HTRG scheme from our previous study. The proposed HTRG scheme is simple and easy to apply in practice by pathologists and might be used as a successful surrogate for longer DFS in patients with potentially resectable PDAC who completed neoadjuvant therapy and surgery.
引用
收藏
页码:1653 / 1660
页数:8
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