Oncological Benefits of Neoadjuvant Chemoradiation With Gemcitabine Versus Upfront Surgery in Patients With Borderline Resectable Pancreatic Cancer

Jin‐Young Jang(Seoul National University Hospital), Youngmin Han(Seoul National University Hospital), Hongeun Lee(Seoul National University Hospital), Sun‐Whe Kim(Samsung Medical Center), Wooil Kwon(Seoul National University Hospital), Kyung-Hun Lee(Seoul National University Hospital), Do‐Youn Oh(Seoul National University Hospital), Eui Kyu Chie(Seoul National University Hospital), Jeong Min Lee(Seoul National University Hospital), Jin Seok Heo(Samsung Medical Center), Joon Oh Park(Samsung Medical Center), Do Hoon Lim(Samsung Medical Center), Seong Hyun Kim(Samsung Medical Center), Sang‐Jae Park(National Cancer Center), Woo Jin Lee(National Cancer Center), Young Hwan Koh(National Cancer Center), Joon Seong Park(Samsung Medical Center), Dong Sup Yoon(Gangnam Severance Hospital), Ik Jae Lee(Samsung Medical Center), Seong Ho Choi(Samsung Medical Center)
Annals of Surgery
February 18, 2018
Cited by 676Open Access
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Abstract

OBJECTIVE: This study was performed to determine whether neoadjuvant treatment increases survival in patients with BRPC. SUMMARY BACKGROUND DATA: Despite many promising retrospective data on the effect of neoadjuvant treatment for borderline resectable pancreatic cancer (BRPC), no high-level evidence exists to support the role of such treatment. METHODS: This phase 2/3 multicenter randomized controlled trial was designed to enroll 110 patients with BRPC who were randomly assigned to gemcitabine-based neoadjuvant chemoradiation treatment (54 Gray external beam radiation) followed by surgery or upfront surgery followed by chemoradiation treatment from four large-volume centers in Korea. The primary endpoint was the 2-year survival rate (2-YSR). Interim analysis was planned at the time of 50% case enrollment. RESULTS: After excluding the patients who withdrew consent (n = 8) from the 58 enrolled patients, 27 patients were allocated to neoadjuvant treatment and 23 to upfront surgery groups. The overall 2-YSR was 34.0% with a median survival of 16 months. In the intention-to-treat analysis, the 2-YSR and median survival were significantly better in the neoadjuvant chemoradiation than the upfront surgery group [40.7%, 21 months vs 26.1%, 12 months, hazard ratio 1.495 (95% confidence interval 0.66-3.36), P = 0.028]. R0 resection rate was also significantly higher in the neoadjuvant chemoradiation group than upfront surgery (n = 14, 51.8% vs n = 6, 26.1%, P = 0.004). The safety monitoring committee decided on early termination of the study on the basis of the statistical significance of neoadjuvant treatment efficacy. CONCLUSION: This is the first prospective randomized controlled trial on the oncological benefits of neoadjuvant treatment in BRPC. Compared to upfront surgery, neoadjuvant chemoradiation provides oncological benefits in patients with BRPC.


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