ArticleClinical journal of gastroenterology2026
Immune checkpoint inhibitor-based chemotherapy for granulocyte-colony stimulating factor-producing advanced esophageal squamous cell carcinoma: a report of three cases.
Article in Clinical journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
introductionGranulocyte-colony stimulating factor (G-CSF)-producing esophageal squamous cell carcinoma (ESCC) is a rare and highly aggressive malignancy. Currently, no specific treatment approach has been established for G-CSF-producing tumors, including those in the lungs, esophagus, and other organs. Here, we present three cases of advanced G-CSF-producing ESCC treated with immune checkpoint inhibitor (ICI) combination chemotherapy. CASE PRESENTATION: Case 1: A 52-year-old man was diagnosed with G-CSF-producing ESCC with multiple lymph node and lung metastases. First-line chemotherapy with fluorouracil (5-FU), cisplatin, and pembrolizumab (FP + PEM) led to significant tumor regression and normalization of inflammatory marker levels. The regimen was de-escalated to 5-FU and pembrolizumab, and the disease remains stable. Case 2: A 69-year-old man was diagnosed with G-CSF-producing ESCC with multiple lymph node metastases. FP + PEM therapy initially reduced the tumor burden, but disease progression occurred after four treatment cycles. The patient was switched to second-line weekly paclitaxel. Case 3: A 62-year-old man was diagnosed with G-CSF-producing ESCC with bone metastasis. FP + PEM therapy achieved partial response in the primary tumor, but bone metastasis progressed, requiring radiation and a switch to paclitaxel.
conclusionsWe report three cases of advanced G-CSF-producing ESCC treated with ICI combination chemotherapy. Although ICIs show promise, treatment resistance remains a challenge. Further research and additional case accumulation are needed to better understand their efficacy and optimize treatment strategies.
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