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Response to Immune Checkpoint Inhibitors in Recurrent or Metastatic Esophageal Squamous Cell Carcinoma May Be Affected by Tumor Sites.
Guo, Jhe-Cyuan; Lin, Chen-Yuan; Lin, Chia-Chi; Huang, Ta-Chen; Lien, Ming-Yu; Lu, Li-Chun; Kuo, Hung-Yang; Hsu, Chih-Hung.
Afiliação
  • Guo JC; Department of Medical Oncology, National Taiwan University Cancer Center, Taipei, Taiwan, jhecyuanguo@gmail.com.
  • Lin CY; Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan, jhecyuanguo@gmail.com.
  • Lin CC; Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan, jhecyuanguo@gmail.com.
  • Huang TC; Division of Hematology and Oncology, China Medical University Hospital, Taichung, Taiwan.
  • Lien MY; Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
  • Lu LC; Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Kuo HY; Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
  • Hsu CH; Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.
Oncology ; 99(10): 652-658, 2021.
Article em En | MEDLINE | ID: mdl-34340231
ABSTRACT

INTRODUCTION:

Heterogeneous tumor response has been reported in cancer patients treated with immune checkpoint inhibitors (ICIs). This study investigated whether the tumor site is associated with the response to ICIs in patients with recurrent or metastatic esophageal squamous cell carcinoma (ESCC).

METHODS:

Patients with ESCC who had measurable tumors in the liver, lung, or lymph node (LN) according to the response evaluation criteria in solid tumors (RECIST) 1.1 and received ICIs at 2 medical centers in Taiwan were enrolled. In addition to RECIST 1.1, tumor responses were determined per individual organ basis according to organ-specific criteria modified from RECIST 1.1. Fisher test or χ2 test was used for statistical analysis.

RESULTS:

In total, 37 patients were enrolled. The overall response rate per RECIST 1.1 was 13.5%. Measurable tumors in the LN, lung, and liver were observed in 26, 17, and 13 patients, respectively. The organ-specific response rates were 26.9%, 29.4%, and 15.4% for the LN, lung, and liver tumors, respectively (p = 0.05). The organ-specific disease control rates were 69.2%, 52.9%, and 21.1% for the LN, lung, and liver tumors, respectively (p = 0.024). Five (27.8%) among 18 patients harboring at least 2 involved organs had heterogeneous tumor response.

CONCLUSION:

The response and disease control to ICIs may differ in ESCC tumors located at different metastatic sites, with a lesser likelihood of response and disease control in metastatic liver tumors than in tumors located at the LNs and lung.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Carcinoma de Células Escamosas do Esôfago / Inibidores de Checkpoint Imunológico Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Carcinoma de Células Escamosas do Esôfago / Inibidores de Checkpoint Imunológico Idioma: En Ano de publicação: 2021 Tipo de documento: Article