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The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.

Lapatinib in Combination With Capecitabine Plus Oxaliplatin in Human Epidermal Growth Factor Receptor 2–Positive Advanced or Metastatic Gastric, Esophageal, or Gastroesophageal Adenocarcinoma: TRIO-013/LOGiC—A Randomized Phase III Trial

Open access
Hecht, J. Randolph, Bang, Yung-Jue, Qin, Shukui K., Chung, Hyun C., Xu, Jianming M., Park, Joon O., Jeziorski, Krzysztof, Shparyk, Yaroslav, Hoff, Paulo M., Sobrero, Alberto, Salman, Pamela, Li, Jin, Protsenko, Svetlana A., Wainberg, Zev A., Buyse, Marc, Afenjar, Karen, Houé, Vincent, Garcia, Agathe, Kaneko, Tomomi, Huang, Yingjie, Khan-Wasti, Saba, Santillana, Sergio, Press, Michael F., Slamon, Dennis·2016·Journal of Clinical Oncology

Abstract

Purpose: To evaluate the efficacy of adding lapatinib to capecitabine and oxaliplatin (CapeOx) in patients with previously untreated human epidermal growth factor receptor 2 (HER2) –amplified advanced gastroesophageal adenocarcinoma. Patients and Methods: Patients with HER2-positive advanced gastroesophageal adenocarcinoma were randomly assigned at a one-to-one ratio to CapeOx plus lapatinib 1,250 mg or placebo daily. Primary end point was overall survival (OS) in patients with centrally confirmed HER2 amplification in the primary efficacy population. Results: A total of 545 patients were randomly assigned, and 487 patients comprised the primary efficacy population. Median OS in the lapatinib and placebo arms was 12.2 (95% CI, 10.6 to 14.2) and 10.5 months (95% CI, 9.0 to 11.3), respectively, which was not significantly different (hazard ratio, 0.91; 95% CI, 0.73 to 1.12). Median progression-free survival in the lapatinib and placebo arms was 6.0 (95% CI, 5.6 to 7.0) and 5.4 months (95% CI, 4.4 to 5.7), respectively (hazard ratio, 0.82; 95% CI, 0.68 to 1.00; P = .0381). Response rate was significantly higher in the lapatinib arm: 53% (95% CI, 46.4 to 58.8) compared with 39% (95% CI, 32.9 to 45.3) in the placebo arm (P = .0031). Preplanned exploratory subgroup analyses showed OS in the lapatinib arm was prolonged in Asian and younger patients. No correlation was observed between HER2 immunohistochemistry status and survival. There were increased toxicities in the lapatinib arm, particularly diarrhea. Conclusion: Addition of lapatinib to CapeOx did not increase OS in patients with HER2-amplified gastroesophageal adenocarcinoma. There were clear differences in the effect of lapatinib depending on region and age. Future studies could examine this correlation.

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Metadata

Authors
Hecht, J. R., Bang, Y.-J., Qin, S. K., Chung, H. C., Xu, J. M., Park, J. O., Jeziorski, K., Shparyk, Y., Hoff, P. M., Sobrero, A., Salman, P., Li, J., Protsenko, S. A., Wainberg, Z. A., Buyse, M., Afenjar, K., Houé, V., Garcia, A., Kaneko, T., Huang, Y., Khan-Wasti, S., Santillana, S., Press, M. F., & Slamon, D.
Venue
Journal of Clinical Oncology
Published
2016-02-10
Volume
34
Issue
5
Pages
443-451
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2185378752
Cited by
624
References
22
FWCI
47.33
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Lapatinib in Combination With Capecitabine Plus Oxaliplatin in Human Epidermal Growth Factor Receptor 2–Positive Advanced or Metastatic Gastric, Esophageal, or Gastroesophageal Adenocarcinoma: TRIO-013/LOGiC—A Randomized Phase III Trial. https://app.cochat.ai/papers/10.1200/jco.2015.62.6598
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Hecht, J. R., Bang, Y.-J., Qin, S. K., Chung, H. C., Xu, J. M., Park, J. O., Jeziorski, K., Shparyk, Y., Hoff, P. M., Sobrero, A., Salman, P., Li, J., Protsenko, S. A., Wainberg, Z. A., Buyse, M., Afenjar, K., Houé, V., Garcia, A., Kaneko, T., . . . Slamon, D. (2016). Lapatinib in Combination With Capecitabine Plus Oxaliplatin in Human Epidermal Growth Factor Receptor 2–Positive Advanced or Metastatic Gastric, Esophageal, or Gastroesophageal Adenocarcinoma: TRIO-013/LOGiC—A Randomized Phase III Trial. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2015.62.6598

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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