Suneel Kamath, Joanna Roopkumar, Ying Ni, Minqian Shen, Pablo Bejarano, Daniela Allende, Arun Nagarajan, Tim Nguyen, Bachar Dergham, Dale Shepard, Marc A Shapiro, Michael J McNamara, Bassam N Estfan, Kanika G Nair, Alok A Khorana
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Clinical data were obtained, and next-generation sequencing was performed. Statistical analyses comparing the 2 groups were performed using descriptive statistics, the Kaplan-Meier method, and the log-rank test.</p><p><strong>Results: </strong>The study comprised 4 exceptional responders and 6 controls. Both groups were well balanced in age, sex, race, and treatment regimens. Exceptional responders had significantly fewer nonsynonymous mutations than controls (2.25 vs 5.17; P = .014). A mutation count of less than 3 was associated with significantly better progression-free survival (17.2 vs 2.3 months; P = .002) and overall survival (29.4 vs 4.6 months; P = .013). Tumor mutational burden did not differ between exceptional responders and controls (4.88 vs 5.70 mut/Mb; P = .39).</p><p><strong>Conclusion: </strong>A lower number of nonsynonymous mutations may correlate with exceptional outcomes in patients with pancreatic cancer. 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引用次数: 0
摘要
简介晚期胰腺癌患者对治疗的特殊反应非常罕见。本研究探讨了典型反应和特殊反应之间可能存在的基因组差异,这些差异可能赋予患者更有利的生物学特性:我们纳入了 2013 年 4 月至 2017 年 8 月期间克利夫兰诊所的晚期胰腺癌特殊应答者和对照组。特殊应答者定义为转移性疾病总生存期超过18个月,局部晚期疾病总生存期超过24个月的患者。获得了临床数据,并进行了新一代测序。采用描述性统计、Kaplan-Meier 法和对数秩检验对两组患者进行了统计分析:研究包括 4 例特殊应答者和 6 例对照组。两组患者在年龄、性别、种族和治疗方案方面都非常均衡。特殊应答者的非同义突变明显少于对照组(2.25 vs 5.17;P = .014)。突变数小于 3 与无进展生存期(17.2 个月 vs 2.3 个月;P = .002)和总生存期(29.4 个月 vs 4.6 个月;P = .013)明显更佳相关。肿瘤突变负荷在特殊应答者和对照组之间没有差异(4.88 vs 5.70 mut/Mb;P = .39):结论:非同义突变数量较少可能与胰腺癌患者的特殊治疗效果有关。结论:较少的非同义突变数量可能与胰腺癌患者的特殊结果相关,这些发现应鼓励未来对特殊反应的基因组特征进行研究。
Genomic Predictors Associated With Exceptional Response to Systemic Therapy in Advanced Pancreatic Cancer.
Introduction: Exceptional response to therapy is rare in patients with advanced pancreatic cancer. This study explored potential genomic differences between typical and exceptional responses that could confer more favorable biology.
Methods: We included exceptional responders and controls with advanced pancreatic cancer from Cleveland Clinic from April 2013 to August 2017. Exceptional responders were defined as patients with an overall survival of more than 18 months for metastatic disease and more than 24 months for locally advanced disease. Clinical data were obtained, and next-generation sequencing was performed. Statistical analyses comparing the 2 groups were performed using descriptive statistics, the Kaplan-Meier method, and the log-rank test.
Results: The study comprised 4 exceptional responders and 6 controls. Both groups were well balanced in age, sex, race, and treatment regimens. Exceptional responders had significantly fewer nonsynonymous mutations than controls (2.25 vs 5.17; P = .014). A mutation count of less than 3 was associated with significantly better progression-free survival (17.2 vs 2.3 months; P = .002) and overall survival (29.4 vs 4.6 months; P = .013). Tumor mutational burden did not differ between exceptional responders and controls (4.88 vs 5.70 mut/Mb; P = .39).
Conclusion: A lower number of nonsynonymous mutations may correlate with exceptional outcomes in patients with pancreatic cancer. These findings should encourage future studies into genomic signatures of exceptional response.
期刊介绍:
Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.