Predictors and survival for pathologic tumor response grade in borderline resectable and locally advanced pancreatic cancer treated with induction chemotherapy and neoadjuvant stereotactic body radiotherapy

被引:76
作者
Mellon, Eric A. [1 ,2 ]
Jin, William H. [1 ]
Frakes, Jessica M. [1 ]
Centeno, Barbara A. [3 ]
Strom, Tobin J. [1 ]
Springett, Gregory M. [4 ]
Malafa, Mokenge P. [4 ]
Shridhar, Ravi [5 ]
Hodul, Pamela J. [4 ]
Hoffe, Sarah E. [1 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Radiat Oncol, Tampa, FL USA
[2] Univ Miami, Miller Sch Med, Sylvester Comprehens Canc Ctr, Dept Radiat Oncol, Miami, FL 33136 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Pathol, Tampa, FL USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Gastrointestinal Tumor Program, Tampa, FL USA
[5] Florida Hosp Canc Inst, Dept Radiat Oncol, Orlando, FL USA
关键词
PREOPERATIVE CHEMORADIOTHERAPY; DUCTAL ADENOCARCINOMA; JUNCTIONAL CANCER; SERUM CA-19-9; THERAPY; CHEMORADIATION; GEMCITABINE; RADIATION; OUTCOMES; TRIAL;
D O I
10.1080/0284186X.2016.1256497
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Neoadjuvant therapy response correlates with survival in multiple gastrointestinal malignancies. To potentially augment neoadjuvant response for pancreas adenocarcinoma, we intensified treatment with stereotactic body radiotherapy (SBRT) following multi-agent chemotherapy. Using this regimen, we analyzed whether the College of American Pathology (CAP) tumor regression grade (TRG) at pancreatectomy correlated with established response biomarkers and survival. Materials and methods: We identified borderline resectable (BRPC) and locally advanced (LAPC) pancreatic cancer patients treated according to our institutional clinical pathway who underwent surgical resection with reported TRG (n = 81, median follow-up after surgery 24.2 months). Patients had baseline CA19-9, computed tomography (CT), endoscopic ultrasound, and FDG positron emission tomography (PET)/CT then underwent multi-agent chemotherapy (79% with three cycles of gemcitabine, docetaxel and capecitabine) followed by 5-fraction SBRT. They then underwent restaging CT, PET/CT and CA19-9. Overall (OS) and progression-free (PFS) survival were estimated and compared by Kaplan-Meier and log-rank methods. Univariate ordinal logistic regression correlated TRG with baseline, restaging and change in CA19-9 and the PET maximum standardized uptake value (SUVmax). Results: Restaging level and decrease in CA19-9 correlated with improved TRG (p=.02 for both) as did restaging SUVmax (p<.01), yet there was no TRG correlation with decrease in SUVmax (p=.10) or CT response (p=.30). The TRG groups had similar OS and PFS except the TRG 0 (complete response) group. Compared to partial response levels (TRG 1-3, median OS 33.9 months, median PFS 13.0 months), the six (7%) patients with TRG 0 had no deaths (p=.05) and only one progression (p=.03). A group of 10 (12%) TRG 1 patients with only residual isolated tumor cells had similar outcomes to the other TRG 1-3 patients. Conclusion: Pre-operative PET-CT and CA19-9 response correlate with histopathologic tumor regression. Patients with complete pathologic response have superior outcomes, suggesting a rationale for intensification and personalization of neoadjuvant therapy in BRPC and LAPC.
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收藏
页码:391 / 397
页数:7
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