Immunotherapy as a new perspective for the therapy of esophageal cancer.

Yvonne Huber, Markus Moehler, Anica H��gner
Author Information
  1. Yvonne Huber: Department of Medicine I, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany. ORCID
  2. Markus Moehler: Department of Medicine I, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
  3. Anica H��gner: Klinik f��r H��matologie, Onkologie und Palliativmedizin, Vivantes Klinikum im Friedrichshain, Berlin, Germany.

Abstract

The therapeutic landscape in nearly every therapeutic line in advanced/metastatic patients with squamous cell carcinoma (SCC) and esophagogastric adenocarcinoma (EGC) is enriched by recent approvals of immune checkpoint inhibitors (ICIs). In curative intended therapy, patients without pathological residual disease of SCC or GEJ (esophagogastric junction) cancer after preoperative chemoradiation and complete resection have access to adjuvant immunotherapy (independent of PD-L1 (programmed cell death protein 1) status, nivolumab, CHECKMATE 577). For metastatic SCC in the first-line, nivolumab combined with chemotherapy or with ipilimumab (TPS (tumor proportion score) ���1���%, SCC, CHECKMATE 648) are approved, as well as second-line nivolumab alone regardless of PD-L1 status (ATTRACTION 03). For both, locally advanced or metastatic SCC and EGC, chemotherapy with pembrolizumab is available for patients with CPS (combined positive score) ���10 (KEYNOTE 590) and for adenocarcinoma with nivolumab (CPS ���5, CHECKMATE 649). Recent added approvals are chemotherapy with pembrolizumab in CPS ���1 patients (KEYNOTE 859) and the addition of trastuzumab for personalized therapy in HER-2 positive/CPS ���1 gastric and GEJ patients (KEYNOTE 811).

Keywords

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Word Cloud

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