Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data

Abstract Background Since the results of the ToGA trial were published, trastuzumab-based chemotherapy has been used as the standard first-line treatment for HER2-positive recurrent or primary metastatic gastric cancer (RPMGC). However, the real-world data has been rarely reported. Therefore, we inv...

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Published in:BMC Cancer
Main Authors: Tae-Hwan Kim, Hun Do Cho, Yong Won Choi, Hyun Woo Lee, Seok Yun Kang, Geum Sook Jeong, Jin-Hyuk Choi, Mi Sun Ahn, Seung-Soo Sheen
Format: Article
Language:English
Published: BMC 2021-03-01
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Online Access:https://doi.org/10.1186/s12885-021-08058-2
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author Tae-Hwan Kim
Hun Do Cho
Yong Won Choi
Hyun Woo Lee
Seok Yun Kang
Geum Sook Jeong
Jin-Hyuk Choi
Mi Sun Ahn
Seung-Soo Sheen
author_facet Tae-Hwan Kim
Hun Do Cho
Yong Won Choi
Hyun Woo Lee
Seok Yun Kang
Geum Sook Jeong
Jin-Hyuk Choi
Mi Sun Ahn
Seung-Soo Sheen
author_sort Tae-Hwan Kim
collection DOAJ
container_title BMC Cancer
description Abstract Background Since the results of the ToGA trial were published, trastuzumab-based chemotherapy has been used as the standard first-line treatment for HER2-positive recurrent or primary metastatic gastric cancer (RPMGC). However, the real-world data has been rarely reported. Therefore, we investigated the outcomes of trastuzumab-based chemotherapy in a single center. Methods This study analyzed the real-world data of 47 patients with HER2-positive RPMGC treated with trastuzumab-based chemotherapy in a single institution. Results With the median follow-up duration of 18.8 months in survivors, the median overall survival (OS) and progression-free survival were 12.8 and 6.9 months, respectively, and the overall response rate was 64%. Eastern Cooperative Oncology Group performance status 2 and massive amount of ascites were independent poor prognostic factors for OS, while surgical resection before or after chemotherapy was associated with favorable OS, in multivariate analysis. In addition, 5 patients who underwent conversion surgery after chemotherapy demonstrated an encouraging median OS of 30.8 months, all with R0 resection. Conclusions Trastuzumab-based chemotherapy in patients with HER2-positive RPMGC in the real world demonstrated outcomes almost comparable to those of the ToGA trial. Moreover, conversion surgery can be actively considered in fit patients with a favorable response after trastuzumab-based chemotherapy.
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spelling doaj-art-e533d210d54042c18dc5b4e6ef42b2bc2025-08-19T19:33:07ZengBMCBMC Cancer1471-24072021-03-012111810.1186/s12885-021-08058-2Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world dataTae-Hwan Kim0Hun Do Cho1Yong Won Choi2Hyun Woo Lee3Seok Yun Kang4Geum Sook Jeong5Jin-Hyuk Choi6Mi Sun Ahn7Seung-Soo Sheen8Department of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Hematology-Oncology, Ajou University School of MedicineDepartment of Pulmonology and Critical Care Medicine, Ajou University School of MedicineAbstract Background Since the results of the ToGA trial were published, trastuzumab-based chemotherapy has been used as the standard first-line treatment for HER2-positive recurrent or primary metastatic gastric cancer (RPMGC). However, the real-world data has been rarely reported. Therefore, we investigated the outcomes of trastuzumab-based chemotherapy in a single center. Methods This study analyzed the real-world data of 47 patients with HER2-positive RPMGC treated with trastuzumab-based chemotherapy in a single institution. Results With the median follow-up duration of 18.8 months in survivors, the median overall survival (OS) and progression-free survival were 12.8 and 6.9 months, respectively, and the overall response rate was 64%. Eastern Cooperative Oncology Group performance status 2 and massive amount of ascites were independent poor prognostic factors for OS, while surgical resection before or after chemotherapy was associated with favorable OS, in multivariate analysis. In addition, 5 patients who underwent conversion surgery after chemotherapy demonstrated an encouraging median OS of 30.8 months, all with R0 resection. Conclusions Trastuzumab-based chemotherapy in patients with HER2-positive RPMGC in the real world demonstrated outcomes almost comparable to those of the ToGA trial. Moreover, conversion surgery can be actively considered in fit patients with a favorable response after trastuzumab-based chemotherapy.https://doi.org/10.1186/s12885-021-08058-2TrastuzumabChemotherapyGastric cancerPrognosis
spellingShingle Tae-Hwan Kim
Hun Do Cho
Yong Won Choi
Hyun Woo Lee
Seok Yun Kang
Geum Sook Jeong
Jin-Hyuk Choi
Mi Sun Ahn
Seung-Soo Sheen
Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
Trastuzumab
Chemotherapy
Gastric cancer
Prognosis
title Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
title_full Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
title_fullStr Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
title_full_unstemmed Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
title_short Trastuzumab-based palliative chemotherapy for HER2-positive gastric cancer: a single-center real-world data
title_sort trastuzumab based palliative chemotherapy for her2 positive gastric cancer a single center real world data
topic Trastuzumab
Chemotherapy
Gastric cancer
Prognosis
url https://doi.org/10.1186/s12885-021-08058-2
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