Histological transformation to signet-ring cell carcinoma in a patient with clinically aggressive poorly differentiated adenocarcinoma of the ascending colon after response to chemotherapy plus cetuximab: a case report

被引:0
作者
Nagano, Hideki [1 ]
Ohyama, Shigekazu [1 ]
Sato, Atsushi [1 ]
Igarashi, Jun [1 ]
Yamamoto, Tomoko [1 ]
Kadoya, Masumi [2 ]
Kobayashi, Mikiko [3 ]
机构
[1] Marunouchi Hosp, Dept Surg, 1-7-45 Nagisa Matsumoto, Nagano 3900841, Japan
[2] Marunouchi Hosp, Dept Radiol, 1-7-45 Nagisa Matsumoto, Nagano 3900841, Japan
[3] Marunouchi Hosp, Dept Pathol, 1-7-45 Nagisa Matsumoto, Nagano 3900841, Japan
关键词
Histological transformation; Poorly differentiated adenocarcinoma; Signet-ring cell carcinoma; Ascending colon cancer; Chemotherapy; Cetuximab; LIQUID BIOPSIES; ACQUIRED-RESISTANCE; EVOLUTION; FEATURES; THERAPY;
D O I
10.1186/s12957-023-03053-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAlteration of chemosensitivity or tumor aggressiveness in response to chemotherapy has been reported, and liquid biopsy assessment during chemotherapy for colorectal cancers has confirmed the acquisition of mutations in various oncogenes. However, the occurrence of histological transformation seems to be extremely rare in colorectal cancers, and the few existing case reports of this transformation are from lung cancer and breast cancer. In this report, we describe the histological transformation of clinically aggressive scirrhous-type poorly differentiated adenocarcinoma of the ascending colon to signet-ring cell carcinoma in almost all recurrent tumors that were confirmed by autopsy after response to chemotherapy plus cetuximab.Case presentationA 59-year-old woman visited our hospital with whole abdominal pain and body weight loss and was diagnosed with scirrhous-type poorly differentiated adenocarcinoma of the ascending colon with aggressive lymph node metastases. The intrinsic chemosensitivity of the tumors was evident upon initiation of mFOLFOX6 plus cetuximab therapy, and right hemicolectomy was performed, and the tumor obviously remained in the peripancreatic area, paraaortic region, or other retroperitoneal areas. The ascending colon tumors mainly consisted of poorly differentiated adenocarcinoma and were not associated with signet-ring cell components except for minute clusters in a few lymphatic emboli in the main tumor. Chemotherapy was continued, and metastases were eliminated at 8 months after the operation; this response was maintained for an additional 4 months. Discontinuation of chemotherapy plus cetuximab resulted in immediate tumor recurrence and rapid expansion, and the patient died of the recurrent tumor 1 year and 2 months after the operation. Autopsy specimens revealed that almost all of the recurrent tumors exhibited transformation and consisted of signet-ring cell histology.ConclusionThis case might suggest that various oncogene mutations or epigenetic changes resulting from chemotherapy, especially regimens that include cetuximab, contribute to the transformation of non-signet-ring cell colorectal carcinoma to signet-ring cell carcinoma histology and can promote the aggressive clinical progression characteristic of signet-ring cell carcinoma.
引用
收藏
页数:11
相关论文
共 26 条
[1]   Clinicopathological and Molecular Characteristics of Colorectal Signet Ring Cell Carcinoma: A Review [J].
An, Yang ;
Zhou, Jiaolin ;
Lin, Guole ;
Wu, Huanwen ;
Cong, Lin ;
Li, Yunhao ;
Qiu, Xiaoyuan ;
Shi, Weikun .
PATHOLOGY & ONCOLOGY RESEARCH, 2021, 27
[2]   Liquid Biopsies, What We Do Not Know (Yet) [J].
Bardelli, Alberto ;
Pantel, Klaus .
CANCER CELL, 2017, 31 (02) :172-179
[3]   Primary signet-ring cell carcinoma of the colorectum [J].
Bittorf, B ;
Merkel, S ;
Matzel, KE ;
Wein, A ;
Dimmler, A ;
Hohenberger, W .
LANGENBECKS ARCHIVES OF SURGERY, 2004, 389 (03) :178-183
[4]   Signet ring cell differentiation in mucinous colorectal carcinoma [J].
Borger, M. E. ;
Gosens, M. J. E. M. ;
Jeuken, J. W. M. ;
van Kempen, L. C. L. T. ;
van de velde, C. J. H. ;
van Krieken, J. H. J. M. ;
Nagtegaal, I. D. .
JOURNAL OF PATHOLOGY, 2007, 212 (03) :278-286
[5]   Genomic characterization of intrinsic and acquired resistance to cetuximab in colorectal cancer patients [J].
Bray, Steven M. ;
Lee, Jeeyun ;
Kim, Seung Tae ;
Hur, Joon Young ;
Ebert, Philip J. ;
Calley, John N. ;
Wulur, Isabella H. ;
Gopalappa, Thejaswini ;
Wong, Swee Seong ;
Qian, Hui-Rong ;
Ting, Jason C. ;
Liu, Jiangang ;
Willard, Melinda D. ;
Novosiadly, Ruslan D. ;
Park, Young Suk ;
Park, Joon Oh ;
Lim, Ho Yeong ;
Kang, Won Ki ;
Aggarwal, Amit ;
Kim, Hee Cheol ;
Reinhard, Christoph .
SCIENTIFIC REPORTS, 2019, 9 (1)
[6]   The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers [J].
Diaz, Luis A., Jr. ;
Williams, Richard T. ;
Wu, Jian ;
Kinde, Isaac ;
Hecht, J. Randolph ;
Berlin, Jordan ;
Allen, Benjamin ;
Bozic, Ivana ;
Reiter, Johannes G. ;
Nowak, Martin A. ;
Kinzler, Kenneth W. ;
Oliner, Kelly S. ;
Vogelstein, Bert .
NATURE, 2012, 486 (7404) :537-540
[7]   Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing [J].
Gerlinger, Marco ;
Rowan, Andrew J. ;
Horswell, Stuart ;
Larkin, James ;
Endesfelder, David ;
Gronroos, Eva ;
Martinez, Pierre ;
Matthews, Nicholas ;
Stewart, Aengus ;
Tarpey, Patrick ;
Varela, Ignacio ;
Phillimore, Benjamin ;
Begum, Sharmin ;
McDonald, Neil Q. ;
Butler, Adam ;
Jones, David ;
Raine, Keiran ;
Latimer, Calli ;
Santos, Claudio R. ;
Nohadani, Mahrokh ;
Eklund, Aron C. ;
Spencer-Dene, Bradley ;
Clark, Graham ;
Pickering, Lisa ;
Stamp, Gordon ;
Gore, Martin ;
Szallasi, Zoltan ;
Downward, Julian ;
Futreal, P. Andrew ;
Swanton, Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (10) :883-892
[8]   Duration of hormone replacement therapy, breast tumour size and grade in a screening programme [J].
Gertig, DM ;
Erbas, B ;
Fletcher, A ;
Amos, A ;
Kavanagh, AM .
BREAST CANCER RESEARCH AND TREATMENT, 2003, 80 (03) :267-273
[9]  
HAMAZAKI M, 1987, ACTA PATHOL JAPON, V37, P1679
[10]   Primary Tumor Location as a Predictive Factor for First-line Bevacizumab Effectiveness in Metastatic Colorectal Cancer Patients [J].
He, Wen-Zhuo ;
Liao, Fang-Xin ;
Jiang, Chang ;
Kong, Peng-Fei ;
Yin, Chen-Xi ;
Yang, Qiong ;
Qiu, Hui-Juan ;
Zhang, Bei ;
Xia, Liang-Ping .
JOURNAL OF CANCER, 2017, 8 (03) :388-394