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.

Biliary tract cancer HER2-positive zanidatamab

Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
08 Aug 2024
Historique:
medline: 8 8 2024
pubmed: 8 8 2024
entrez: 8 8 2024
Statut: aheadofprint

Résumé

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. 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%). 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. 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.

Autres résumés

Type: plain-language-summary (eng)
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.

Identifiants

pubmed: 39114870
doi: 10.1080/14796694.2024.2368952
doi:

Banques de données

ClinicalTrials.gov
['NCT04466891']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

James J Harding (JJ)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jia Fan (J)

Zhongshan Hospital of Fudan University, Shanghai, China.

Do-Youn 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.

Hye Jin Choi (HJ)

Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.

Jin Won Kim (JW)

Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, South Korea.

Heung-Moon Chang (HM)

Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Lequn Bao (L)

Hubei Cancer Hospital, Wuhan, Hubei, China.

Hui-Chuan Sun (HC)

Zhongshan Hospital of Fudan University, Shanghai, China.

Teresa Macarulla (T)

Vall d´Hebrón University Hospital, Vall d´Hebrón Institute of Oncology (VHIO), Barcelona, Spain.

Feng Xie (F)

The Third Affiliated Hospital of the Chinese people's Liberation army Naval Military Medical University, Shanghai, China.

Jean-Phillippe Metges (JP)

CHRU de Brest - Hopital Morvan, ARPEGO Network, Brest, France.

Jie'er Ying (J)

Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China.

John Bridgewater (J)

University College London Cancer Institute, London, UK.

Myung-Ah Lee (MA)

The Catholic University of Korea, Seoul St Mary's Hospital, Seoul, South Korea.

Mohamedtaki A Tejani (MA)

AdventHealth, Altamonte Springs, FL, USA.

Emerson Y Chen (EY)

Oregon Health & Science University, Portland, OR, USA.

Dong Uk Kim (DU)

Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.

Harpreet Wasan (H)

Hammersmith Hospital, Imperial College London, London, UK.

Michel Ducreux (M)

Université Paris-Saclay, Gustave Roussy, Villejuif, France.

Yuanyuan Bao (Y)

BeiGene, Beijing, China.

Stacie Lindsey (S)

Cholangiocarcinoma Foundation, UT, USA.

Melinda Bachini (M)

Cholangiocarcinoma Foundation, UT, USA.

Helen Morement (H)

AMMF - The Cholangiocarcinoma Charity, Stansted, UK.

Lisa Boyken (L)

Zymeworks Inc., Vancouver, BC, Canada.

Jiafang Ma (J)

BeiGene, Beijing, China.

Phillip Garfin (P)

Jazz Pharmaceuticals, Palo Alto, CA, USA.

Shubham Pant (S)

MD Anderson Cancer Center, Houston, TX, USA.

Classifications MeSH