Using Tumor-Informed Circulating Tumor DNA (ctDNA)-Based Testing for Patients with Anal Squamous Cell Carcinoma

被引:8
作者
Azzi, Georges [1 ]
Tavallai, Mehrad [2 ]
Aushev, Vasily N. [2 ]
Koyen Malashevich, Allyson [2 ]
Botta, Gregory P. [3 ]
Tejani, Mohamedtaki A. [4 ]
Hanna, Diana [5 ]
Krinshpun, Shifra [2 ]
Malhotra, Meenakshi [2 ]
Jurdi, Adham [2 ]
Aleshin, Alexey [2 ]
Kasi, Pashtoon M. [6 ,7 ]
机构
[1] HolyCross Med Grp, Ft Lauderdale, FL USA
[2] Natera Inc, Austin, TX USA
[3] UC San Diego Hlth, San Diego, CA USA
[4] AdventHlth Canc Inst, Orlando, FL USA
[5] USC Norris Comprehens Canc Ctr, Los Angeles, CA USA
[6] Weill Cornell Med, New York, NY USA
[7] NewYork Presbyterian Hosp, Meyer Canc Ctr, Englander Inst Precis Med, Weill Cornell Med,Dept Med Oncol & Hematol, New York, NY 10021 USA
关键词
circulating tumor DNA; anal squamous cell carcinoma; prognostic biomarker; minimal; molecular residual disease; CANCER;
D O I
10.1093/oncolo/oyac249
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Anal squamous cell carcinoma (SCCA) is an uncommon malignancy with a rising incidence that has a high cure rate in its early stages. There is an unmet need for a reliable method to monitor response to treatment and assist in surveillance. Circulating tumor DNA (ctDNA) testing has shown great promise in other solid tumors for monitoring disease progression and detecting relapse in real time. This study aimed to determine the feasibility and use of personalized and tumor-informed ctDNA testing in SCCA. Patients and Methods We analyzed real-world data from 251 patients (817 plasma samples) with stages I-IV SCCA, collected between 11/5/19 and 5/31/22. The tumor genomic landscape and feasibility of ctDNA testing was examined for all patients. The prognostic value of longitudinal ctDNA testing was assessed in patients with clinical follow-up (N = 37). Results Whole-exome sequencing analysis revealed PIK3CA as the most commonly mutated gene, and no associations between mutations and stage. Anytime ctDNA positivity and higher ctDNA levels (MTM/mL) were associated with metastatic disease (P = .004). For 37 patients with clinical follow-up, median follow-up time was 21.0 months (range: 4.1-67.3) post-diagnosis. For patients with stages I-III disease, anytime ctDNA-positivity after definitive treatment was associated with reduced DFS (HR: 28.0; P = .005). Conclusions Our study demonstrates the feasibility of personalized and tumor-informed ctDNA testing as an adjunctive tool in patients with SCCA as well as potential use for detection of molecular/minuteimal residual disease, and relapse during surveillance. Prospective studies are needed to better evaluate the use of ctDNA testing in this indication. Circulating tumor DNA (ctDNA) testing has shown great promise in solid tumors for monitoring disease progression and detecting relapse in real time. This article reports on the feasibility and use of personalized and tumor-informed ctDNA testing specific to anal squamous cell carcinoma. Exploratory analysis from whole exome sequencing (WES; N=251) is also reported.
引用
收藏
页码:220 / 229
页数:10
相关论文
共 29 条
[21]   Landscape of Phosphatidylinositol-3-Kinase Pathway Alterations Across 19 784 Diverse Solid Tumors [J].
Millis, Sherri Z. ;
Ikeda, Sadakatsu ;
Reddy, Sandeep ;
Gatalica, Zoran ;
Kurzrock, Razelle .
JAMA ONCOLOGY, 2016, 2 (12) :1565-1573
[22]   Circulating Tumor DNA in Advanced Anal Cancer: A Blood Biomarker Goes Viral [J].
Morris, Van K. .
CLINICAL CANCER RESEARCH, 2019, 25 (07) :2030-2032
[23]   Nivolumab for previously treated unresectable metastatic anal cancer (NCI9673): a multicentre, single-arm, phase 2 study [J].
Morris, Van K. ;
Salem, Mohamed E. ;
Nimeiri, Halla ;
Iqbal, Syma ;
Singh, Preet ;
Ciombor, Kristen ;
Polite, Blase ;
Deming, Dustin ;
Chan, Emily ;
Wade, James L. ;
Xiao, Lianchun ;
Bekaii-Saab, Tanios ;
Vence, Luis ;
Blando, Jorge ;
Mahvash, Armeen ;
Foo, Wai Chin ;
Ohaji, Chimela ;
Pasia, Manolo ;
Bland, Gail ;
Ohinata, Aki ;
Rogers, Jane ;
Mehdizadeh, Amir ;
Banks, Kimberly ;
Lanman, Richard ;
Wolff, Robert A. ;
Streicher, Howard ;
Allison, James ;
Sharma, Padmanee ;
Eng, Cathy .
LANCET ONCOLOGY, 2017, 18 (04) :446-453
[24]   Squamous cell carcinoma of the anal canal [J].
Morton, Michael ;
Melnitchouk, Nelya ;
Bleday, Ronald .
CURRENT PROBLEMS IN CANCER, 2018, 42 (05) :486-492
[25]  
Oki, 2022, SOC SURG ONCOLOGY
[26]   Squamous cell anal cancer: Management and therapeutic options [J].
Pessia, Beatrice ;
Romano, Lucia ;
Giuliani, Antonio ;
Lazzarin, Gianni ;
Carlei, Francesco ;
Schietroma, Mario .
ANNALS OF MEDICINE AND SURGERY, 2020, 55 :36-46
[27]   ctDNA guiding adjuvant immunotherapy in urothelial carcinoma [J].
Powles, Thomas ;
Assaf, Zoe June ;
Davarpanah, Nicole ;
Banchereau, Romain ;
Szabados, Bernadett E. ;
Yuen, Kobe C. ;
Grivas, Petros ;
Hussain, Maha ;
Oudard, Stephane ;
Gschwend, Jurgen E. ;
Albers, Peter ;
Castellano, Daniel ;
Nishiyama, Hiroyuki ;
Daneshmand, Siamak ;
Sharma, Shruti ;
Zimmermann, Bernhard G. ;
Sethi, Himanshu ;
Aleshin, Alexey ;
Perdicchio, Maurizio ;
Zhang, Jingbin ;
Shames, David S. ;
Degaonkar, Viraj ;
Shen, Xiaodong ;
Carter, Corey ;
Bais, Carlos ;
Bellmunt, Joaquim ;
Mariathasan, Sanjeev .
NATURE, 2021, 595 (7867) :432-+
[28]   Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer [J].
Reinert, Thomas ;
Henriksen, Tenna Vesterman ;
Christensen, Emil ;
Sharma, Shruti ;
Salari, Raheleh ;
Sethi, Himanshu ;
Knudsen, Michael ;
Nordentoft, Iver ;
Wu, Hsin-Ta ;
Tin, Antony S. ;
Rasmussen, Mads Heilskov ;
Vang, Soren ;
Shchegrova, Svetlana ;
Johansen, Amanda Frydendahl Boll ;
Srinivasan, Ramya ;
Assaf, Zoe ;
Balcioglu, Mustafa ;
Olson, Alexander ;
Dashner, Scott ;
Hafez, Dina ;
Navarro, Samantha ;
Goel, Shruti ;
Rabinowitz, Matthew ;
Billings, Paul ;
Sigurjonsson, Styrmir ;
Dyrskjot, Lars ;
Swenerton, Ryan ;
Aleshin, Alexey ;
Laurberg, Soren ;
Madsen, Anders Husted ;
Kannerup, Anne-Sofie ;
Stribolt, Katrine ;
Krag, Soren Palmelund ;
Iversen, Lene H. ;
Sunesen, Kare Gotschalck ;
Lin, Cheng-Ho Jimmy ;
Zimmermann, Bernhard G. ;
Andersen, Claus Lindbjerg .
JAMA ONCOLOGY, 2019, 5 (08) :1124-1131
[29]   Double PIK3CA mutations in cis increase oncogenicity and sensitivity to PI3Kα inhibitors [J].
Vasan, Neil ;
Razavi, Pedram ;
Johnson, Jared L. ;
Shao, Hong ;
Shah, Hardik ;
Antoine, Alesia ;
Ladewig, Erik ;
Gorelick, Alexander ;
Lin, Ting-Yu ;
Toska, Eneda ;
Xu, Guotai ;
Kazmi, Abiha ;
Chang, Matthew T. ;
Taylor, Barry S. ;
Dickler, Maura N. ;
Jhaveri, Komal ;
Chandarlapaty, Sarat ;
Rabadan, Raul ;
Reznik, Ed ;
Smith, Melissa L. ;
Sebra, Robert ;
Schimmoller, Frauke ;
Wilson, Timothy R. ;
Friedman, Lori S. ;
Cantley, Lewis C. ;
Scaltriti, Maurizio ;
Baselga, Jose .
SCIENCE, 2019, 366 (6466) :714-+