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Chemotherapy-induced transient CEA and CA19-9 surges in patients with metastatic or recurrent gastric cancer

Cited 25 time in Web of Science Cited 30 time in Scopus
Authors

Kim, Hye Jin; Lee, Keun-Wook; Kim, Yu Jung; Oh, Do-youn; Kim, Jee Hyun; Im, Seock-ah; Lee, Jong Seok

Issue Date
2009
Publisher
Taylor & Francis
Citation
Acta Oncologica, Vol.48 No.3, pp.385-390
Abstract
Background. Rising serum tumor markers after chemotherapy are generally considered to indicate tumor progression. However, we have observed a transient increase in carcinoembryonic antigen (CEA) or carbohydrate antigen 19-9 (CA19-9) levels despite clinical benefits from chemotherapy in patients with metastatic or recurrent gastric cancer (MRGC). Therefore, this study was performed to determine the incidence of CEA and CA19-9 surges and their implications on the clinical outcome in MRGC patients. Material and methods. Fifty-one and 40 patients who had evaluable data for CEA or CA19-9 surges, respectively, were included. Both CEA and CA 19-9 surges were defined as a 20% increase in these tumor markers from the baseline that was followed by a 20% drop in subsequent levels compared to the baseline. Results. Of 51 evaluable patients for CEA surges, nine patients (18%) had documented CEA surges. The median time to CEA peak and the duration of the CEA surge were 2.8 (1.77.0) and 9.1 weeks (7.621.0), respectively. Of 40 evaluable patients for CA19-9 surges, seven patients (18%) had CA19-9 surges. The median time to peak and the duration of the CA19-9 surge were 2.3 (1.96.0) and 7.1 weeks (4.316.1), respectively. All patients with CEA or CA19-9 surges had radiographic evidence of benefits from chemotherapy. Conclusion. CEA or CA19-9 surges can be observed in MRGC patients receiving chemotherapy. All patients with these surge phenomena had clinical benefits from chemotherapy. An initial rise in CEA or CA19-9 levels after initiation of chemotherapy should not be used as an indicator of progressive disease.
ISSN
0284-186X
URI
https://hdl.handle.net/10371/177152
DOI
https://doi.org/10.1080/02841860802446761
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  • Department of Medicine
Research Area Clinical Medicine

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