Prognostic value of tumor-infiltrating CD163 + macrophage in patients with metastatic gastric cancer undergoing multidisciplinary treatment

The multidisciplinary treatment including induction chemotherapy plus conversion surgery (CS) has attracted attention as a new strategy to improve the outcome of metastatic gastric cancer (MGC). However, it is unclear which patients achieve a good response to chemotherapy and successful CS. Tumor-in...

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Veröffentlicht in:BMC cancer 2022-06, Vol.22 (1), p.608-608, Article 608
Hauptverfasser: Kinoshita, Jun, Fushida, Sachio, Yamaguchi, Takahisa, Moriyama, Hideki, Saito, Hiroto, Shimada, Mari, Terai, Shiro, Okamoto, Koichi, Nakamura, Keishi, Ninomiya, Itasu, Yagi, Shintaro, Inaki, Noriyuki
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Sprache:eng
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Zusammenfassung:The multidisciplinary treatment including induction chemotherapy plus conversion surgery (CS) has attracted attention as a new strategy to improve the outcome of metastatic gastric cancer (MGC). However, it is unclear which patients achieve a good response to chemotherapy and successful CS. Tumor-infiltrating immune cells (TIICs) have been reported to be both prognostic and predictive biomarkers not only in immunotherapy but also in chemotherapy in many cancer types. However, there have been no reports on the usefulness of TIICs as biomarkers in conversion surgery for MGC. The aim of the present study was to evaluate the association between the TIICs and treatment outcome for the multidisciplinary treatment in MGC. We retrospectively analyzed 68 MGC patients who received docetaxel plus cisplatin plus S-1 (DCS) therapy between April 2006 and March 2019 in our institute. The number of tumor-infiltrating CD4 , CD8 , Foxp3 lymphocytes, CD68 , CD163 macrophages in pre-treatment endoscopic biopsy samples were evaluated to investigate their predictive value for multidisciplinary treatment. Fifty patients underwent CS following DCS therapy (CS group), whereas 18 patients underwent DCS therapy alone (non-CS group). The median survival time (MST) of CS group was 33.3 months, which was significantly longer than the MST of 9.0 months in non-CS group (p 
ISSN:1471-2407
1471-2407
DOI:10.1186/s12885-022-09713-y