Literature DB >> 32588692

Treatment of esophageal cancer with multiple liver metastases: a case experience of sustained complete response.

Jiangfang Wang1, Chaoyang Xu2.   

Abstract

Esophageal squamous cell cancer with distant metastases has a poor prognosis. The metastatic sites usually involve the liver, bones, and lungs. Treatment of metastatic disease is essentially palliative and based on chemoradiotherapy. A 57-year-old man with a solitary metastatic mass of 82 × 58 mm in the left liver was treated on 19 October 2012. Irinotecan and cisplatin combination chemotherapy and nimotuzumab targeted therapy were administered. The liver metastatic mass was treated by stereotactic Gamma Knife radiosurgery. Complete remission of the primary disease and hepatic lesion was achieved, and no local or distant recurrence was found during the 7-year follow-up. Because extrahepatic lesions were ruled out and the local disease was completely locoregionally controlled, the use of stereotactic Gamma Knife radiosurgery to remove the hepatic lesion was justified and produced a reasonable outcome.

Entities:  

Keywords:  Metastases; complete response; esophageal squamous cell cancer; liver mass; prognosis; stereotactic radiosurgery

Mesh:

Year:  2020        PMID: 32588692      PMCID: PMC7323305          DOI: 10.1177/0300060520935214

Source DB:  PubMed          Journal:  J Int Med Res        ISSN: 0300-0605            Impact factor:   1.671


Introduction

Esophageal squamous cell cancer (EPC) is a tumor with a poor prognosis, and the median survival time is only about 6 months. Treatments including radiotherapy, targeted therapy, and chemotherapy have made only limited progress in improving the generally disappointing outcomes in recent years.[1] Targeted therapy is a useful treatment approach in breast cancer, lung cancer, and gastric cancer, but targeted therapy in esophageal cancer is still poorly defined.[2,3] We herein report a case of EPC with large liver metastases that was successfully treated with radiotherapy, chemotherapy, and targeted therapy.

Case report

A 57-year-old man presented with a left liver mass of 82 × 58 mm that had been detected by B-mode ultrasonography. He had a history of untreated esophageal cancer and exhibited no progressive dysphagia, pain behind the sternum, melena, or bloody stool. Gastroscopy revealed irregular mucosal processes leading into the lumen, producing surface irregularity, erosion, and congestion about 35 cm from the teeth in the medial and lower esophagus (Figure 1). Histopathological examination revealed EPC (Figure 2(a)). Immunohistochemistry examination showed positive expression of epidermal growth factor receptor (EGFR) (Figure 2(b)). Abdominal computed tomography showed thickening of the medial and lower esophageal wall, many metastatic lymph nodes in the cardia, and several hepatic masses (Figure 3(a), (c)). Abdominal B-ultrasound showed that the liver size was within the normal range and that its capsule was smooth. The distribution of ultrasonic light spots was uniform. The left liver contained an 82- × 58-mm mass and the right liver contained an 87- × 75-mm mass; both had well-defined boundaries and slight hyperechogenicity. According to the American Joint Committee on Cancer Staging, the EPC was stage IV (T3N1M1). Irinotecan and cisplatin chemotherapy was administered, and nimotuzumab targeted therapy was given every 3 weeks for 3 cycles. The diameter of the hepatic lesions significantly decreased along with a remarkable reduction of the EPC by the end of the chemotherapy and targeted therapy sessions (Figure 3(b)). The concurrent liver metastases were treated by stereotactic Gamma Knife radiosurgery (Figure 3(d)). No evidence of other organ metastasis was found during the 7-year follow-up.
Figure 1.

Gastroscopy showed esophageal squamous cell cancer about 35 cm from the teeth in the medial and lower esophagus.

Figure 2.

(a) Histopathological examination revealed esophageal squamous cell cancer (hematoxylin and eosin, ×100). (b) Immunohistochemistry showed positive expression of epidermal growth factor receptor. (c) Negative control (negative expression of epidermal growth factor receptor).

Figure 3.

Abdominal computed tomography showed the medial and lower esophageal wall (a) before treatment and (b) after treatment and the liver metastases (c) before treatment and (d) after treatment. The arrows indicate the locations of the esophageal lesion and liver metastatic lesion.

Gastroscopy showed esophageal squamous cell cancer about 35 cm from the teeth in the medial and lower esophagus. (a) Histopathological examination revealed esophageal squamous cell cancer (hematoxylin and eosin, ×100). (b) Immunohistochemistry showed positive expression of epidermal growth factor receptor. (c) Negative control (negative expression of epidermal growth factor receptor). Abdominal computed tomography showed the medial and lower esophageal wall (a) before treatment and (b) after treatment and the liver metastases (c) before treatment and (d) after treatment. The arrows indicate the locations of the esophageal lesion and liver metastatic lesion. This study was approved by the Ethics Committee of the First Affiliated Hospital of Shaoxing University, Shaoxing People’s Hospital. The patient and his relative provided consent for publication of this report.

Discussion

The liver is one of the main sites of metastasis from EPC.[4] Autopsy data show that considerable numbers of patients with EPC die of liver metastasis. The standard palliative treatment for metastatic EPC is combined chemotherapy. In the present case, neoadjuvant treatment was given with a targeted drug (cetuximab) and combined chemotherapy (paclitaxel and cisplatin), and partial remission was achieved as shown by the decrease in the diameter of the EPC and hepatic lesions. In some studies, the response rate to irinotecan and cisplatin combination chemotherapy for EPC with metastasis was about 30%, with median progression-free survival of 4.5 months and overall survival of 8.8 months.[5,6] Lee et al.[7] assessed the efficacy irinotecan and cisplatin in 32 patients with metastatic EPC. The results showed that 31.3% of patients achieved a partial response, with median progression-free survival of 4.4 months and overall survival of 9.6 months.[7] There is increasing evidence that combination chemotherapy with irinotecan and cisplatin may be well tolerated and can be an effective treatment option for patients with EPC. EGFR is a member of the ErbB receptor tyrosine kinase family and is overexpressed in many types of tumors, including colorectal cancer, lung cancer, breast cancer, and nasopharyngeal cancer.[8,9] EGFR expression is associated with a poor prognosis. Nimotuzumab is a humanized anti-EGFR monoclonal antibody. In recent years, nimotuzumab has been used to treat head and neck squamous cell carcinoma and nasopharyngeal carcinoma.[10] In some studies, nimotuzumab downregulated the expression of EGFR in esophageal squamous cell carcinoma and correlated downstream genes to inhibit the growth of EGFR-positive cells and increase cell sensitivity to chemotherapy or radiotherapy.[11] In the present case, nimotuzumab in combination with irinotecan and cisplatin was well tolerated in the treatment for EPC with liver metastases. In conclusion, a patient with EPC with liver metastasis at the time of diagnosis underwent treatment with nimotuzumab in combination with irinotecan and cisplatin. Because extrahepatic lesions were ruled out and the local disease was completely locoregionally controlled, stereotactic Gamma Knife radiosurgery to remove the hepatic lesions was justified and produced a reasonable outcome.
  11 in total

1.  Trastuzumab With S-1 Plus Cisplatin in HER2-positive Advanced Gastric Cancer Without Measurable Lesions: OGSG 1202.

Authors:  Shunji Endo; Yukinori Kurokawa; Makio Gamoh; Yutaka Kimura; Jin Matsuyama; Hirokazu Taniguchi; Atsushi Takeno; Ryohei Kawabata; Junji Kawada; Toru Masuzawa; Kazuyoshi Yamamoto; Kouji Kobayashi; Daisuke Sakai; Toshio Shimokawa; Taroh Satoh
Journal:  Anticancer Res       Date:  2019-02       Impact factor: 2.480

2.  Cetuximab plus cisplatin, irinotecan, and thoracic radiotherapy as definitive treatment for locally advanced, unresectable esophageal cancer: a phase-II study of the SWOG (S0414).

Authors:  Michael B Tomblyn; Bryan H Goldman; Charles R Thomas; Jacqueline K Benedetti; Heinz-Josef Lenz; Vivek Mehta; Thaddeus Beeker; Philip J Gold; James L Abbruzzese; Charles D Blanke
Journal:  J Thorac Oncol       Date:  2012-05       Impact factor: 15.609

3.  A phase II trial of modified weekly irinotecan and cisplatin for chemotherapy-naïve patients with metastatic or recurrent squamous cell carcinoma of the esophagus.

Authors:  Dae Ho Lee; Heung Tae Kim; Ji-Youn Han; Sung Young Lee; Sung Jin Yoon; Hyae Young Kim; Jin Soo Lee
Journal:  Cancer Chemother Pharmacol       Date:  2007-04-28       Impact factor: 3.333

4.  Treatment outcome for nasopharyngeal carcinoma in University Malaya Medical Centre from 2004-2008.

Authors:  Vincent Chee Ee Phua; Wei Hoong Loo; Mastura Md Yusof; Wan Zamaniah Wan Ishak; Lye Mun Tho; Ngie Min Ung
Journal:  Asian Pac J Cancer Prev       Date:  2013

5.  Nimotuzumab plus chemotherapy with docetaxel, cisplatin, 5-fluorouracil for locally advanced head and neck squamous cell carcinoma: A clinical study.

Authors:  Xing Wang; Jianmin Gu; Cuiling Shao; Kun Han; Jian Meng
Journal:  J Cancer Res Ther       Date:  2019       Impact factor: 1.805

6.  Phase II Study of Irinotecan and Cisplatin Combination Chemotherapy in Metastatic, Unresectable Esophageal Cancer.

Authors:  Miso Kim; Bhumsuk Keam; Tae-Min Kim; Hoon-Gu Kim; Jin-Soo Kim; Sung Sook Lee; Seong Hoon Shin; Min Kyoung Kim; Keon Uk Park; Dong-Wan Kim; Hwan Jung Yun; Jong Seok Lee; Dae Seog Heo
Journal:  Cancer Res Treat       Date:  2016-07-28       Impact factor: 4.679

7.  Optimal Modality for Detecting Distant Metastasis in Primary Nasopharyngeal Carcinoma during Initial Staging: A Systemic Review and Meta-analysis of 1774 Patients.

Authors:  Cheng Xu; Yuan Zhang; Liang Peng; Xu Liu; Wen-Fei Li; Ying Sun; Xu Zhang; Xiao-Ping Lin; Qing Liu; Jun Ma
Journal:  J Cancer       Date:  2017-04-10       Impact factor: 4.207

8.  AURKB as a target in non-small cell lung cancer with acquired resistance to anti-EGFR therapy.

Authors:  Jordi Bertran-Alamillo; Valérie Cattan; Marie Schoumacher; Jordi Codony-Servat; Ana Giménez-Capitán; Frédérique Cantero; Mike Burbridge; Sonia Rodríguez; Cristina Teixidó; Ruth Roman; Josep Castellví; Silvia García-Román; Carles Codony-Servat; Santiago Viteri; Andrés-Felipe Cardona; Niki Karachaliou; Rafael Rosell; Miguel-Angel Molina-Vila
Journal:  Nat Commun       Date:  2019-04-18       Impact factor: 14.919

9.  Broad-spectrum receptor tyrosine kinase inhibitors overcome de novo and acquired modes of resistance to EGFR-targeted therapies in colorectal cancer.

Authors:  Ramona Graves-Deal; Galina Bogatcheva; Saba Rehman; Yuanyuan Lu; James N Higginbotham; Bhuminder Singh
Journal:  Oncotarget       Date:  2019-02-12

10.  Expression of Lin28 is correlated with prognosis and expression of HER-2 and steroid receptors in breast cancer.

Authors:  Chaoyang Xu; Shuxun Jin; Liming Huang
Journal:  Onco Targets Ther       Date:  2019-02-08       Impact factor: 4.147

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