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A plain language summary of the results from the phase 2b HERIZON-BTC-01 study of zanidatamab in participants with HER2-amplified biliary tract cancer.
Harding, James J; Fan, Jia; Oh, Do-Youn; Choi, Hye Jin; Kim, Jin Won; Chang, Heung-Moon; Bao, Lequn; Sun, Hui-Chuan; Macarulla, Teresa; Xie, Feng; Metges, Jean-Phillippe; Ying, Jie'er; Bridgewater, John; Lee, Myung-Ah; Tejani, Mohamedtaki A; Chen, Emerson Y; Kim, Dong Uk; Wasan, Harpreet; Ducreux, Michel; Bao, Yuanyuan; Lindsey, Stacie; Bachini, Melinda; Morement, Helen; Boyken, Lisa; Ma, Jiafang; Garfin, Phillip; Pant, Shubham.
Affiliation
  • Harding JJ; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Fan J; Zhongshan Hospital of Fudan University, Shanghai, China.
  • Oh DY; Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Integrated Major in Innovative Medical Science, Seoul National University Graduate School, Seoul, South Korea.
  • Choi HJ; Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
  • Kim JW; Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, South Korea.
  • Chang HM; Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Bao L; Hubei Cancer Hospital, Wuhan, Hubei, China.
  • Sun HC; Zhongshan Hospital of Fudan University, Shanghai, China.
  • Macarulla T; Vall d´Hebrón University Hospital, Vall d´Hebrón Institute of Oncology (VHIO), Barcelona, Spain.
  • Xie F; The Third Affiliated Hospital of the Chinese people's Liberation army Naval Military Medical University, Shanghai, China.
  • Metges JP; CHRU de Brest - Hopital Morvan, ARPEGO Network, Brest, France.
  • Ying J; Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China.
  • Bridgewater J; University College London Cancer Institute, London, UK.
  • Lee MA; The Catholic University of Korea, Seoul St Mary's Hospital, Seoul, South Korea.
  • Tejani MA; AdventHealth, Altamonte Springs, FL, USA.
  • Chen EY; Oregon Health & Science University, Portland, OR, USA.
  • Kim DU; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Wasan H; Hammersmith Hospital, Imperial College London, London, UK.
  • Ducreux M; Université Paris-Saclay, Gustave Roussy, Villejuif, France.
  • Bao Y; BeiGene, Beijing, China.
  • Lindsey S; Cholangiocarcinoma Foundation, UT, USA.
  • Bachini M; Cholangiocarcinoma Foundation, UT, USA.
  • Morement H; AMMF - The Cholangiocarcinoma Charity, Stansted, UK.
  • Boyken L; Zymeworks Inc., Vancouver, BC, Canada.
  • Ma J; BeiGene, Beijing, China.
  • Garfin P; Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Pant S; MD Anderson Cancer Center, Houston, TX, USA.
Future Oncol ; : 1-11, 2024 Aug 08.
Article in En | MEDLINE | ID: mdl-39114870
ABSTRACT
WHAT IS THIS SUMMARY ABOUT? Researchers wanted to study whether the research drug zanidatamab could help people with a type of cancer called biliary tract cancer. In some people, biliary tract cancer cells make extra copies of a gene called HER2 (also called ERBB2). This is known as being HER2-amplified. Zanidatamab is an antibody designed to destroy cancer cells that have higher-than-normal HER2 protein or gene levels. Zanidatamab is currently under research and is not yet approved for any diseases. Participants in this phase 2b clinical study had tumors that were HER2-amplified and at the advanced or metastatic stage. Participants also had cancer which had become worse after previous chemotherapy or had side effects that were too bad to continue chemotherapy. They also had to meet other requirements to be enrolled. Researchers measured the amount of HER2 protein in the tumor samples of the participants who were enrolled. There were 80 participants with tumors that were both HER2 amplified and had higher-than-normal HER2 protein amounts (considered to be 'HER2-positive'). There were 7 participants with tumors that were HER2-amplified, but had little-to-no levels of the HER2 protein (considered to be 'HER2-low'). All participants in the study were treated with zanidatamab and no other cancer treatments once every 2 weeks. WHAT ARE THE KEY TAKEAWAYS? In the HER2-positive group, 33 of 80 (41%) participants had their tumors shrink by 30% or more of their original size. In half of these participants, their tumors did not grow for 13 months or longer. No participant in the HER2-low group had their tumors shrink by 30% or more. In total, 63 of 87 participants (72%) had at least one side effect believed to be related to zanidatamab treatment. Most side effects were mild or moderate in severity. No participant died from complications related to zanidatamab. Diarrhea was one of the more common side effects and was experienced by 32 of 87 participants (37%). Side effects related to receiving zanidatamab through the vein, such as chills, fever, or high blood pressure, were experienced by 29 of 87 participants (33%). WHAT ARE THE CONCLUSIONS REPORTED BY THE RESEARCHERS? The results of this study support the potential for zanidatamab as a new therapy for people with HER2-positive biliary tract cancer after they had already received chemotherapy. More research is occurring to support these results.Clinical Trial Registration NCT04466891 (HERIZON-BTC-01 study).
The HERIZON-BTC-01 study revealed zanidatamab as a potentially effective treatment for HER2-positive biliary tract cancer after standard chemotherapy fails. Read more in the lay summary by @hardingjjmd, @DrShubhamPant, and coauthors. #BiliaryTractCancer #HER2 #zanidatamab.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Future Oncol Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Language: En Journal: Future Oncol Year: 2024 Type: Article Affiliation country: United States