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Expert Interview

Slingshot members are talking to an expert! The topic is:

Discussing Zymeworks’ Zanidatamab (ZW25) in HER2-positive biliary tract cancers (BTCs) with topline data from the HERIZON-BTC-01 Trial

Ticker(s): ZYME

Who's the expert?

Institution: Duke University

  • Instructor of Medical Oncology at Duke who treats gastrointestinal cancers and conducts research on tumor immunology and immunotherapy, particularly for melanoma and gastrointestinal malignancies.
  • Laboratory and translational research is focused on tumor immune evasion and immunotherapy resistances, and the development of biomarkers with a specific interest in dendritic cell tolerance.
  • Research and clinical goal of finding new immunotherapeutic options for patients with supportive biomarkers to identify patients.

Interview Questions
Q1.

Please describe your practice as a clinician,how many patients with   Cholangiocarcinoma/biliary tract cancers do you see on a yearly basis? What percent are HER2-positive? Could you walk us through the standard of care, and take us through the most promising upcoming treatments, or interesting clinical trials in this space?

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Q2.

Considering there’s no approved HER2-targeted therapy for the treatment of BTC, what is your approach in treating those cases?

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Q3.

How much of an unmet need is there in HER2-positive cholangiocarcinoma?

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Q4.

Please discuss the new Phase 2b Topline Data In The Pivotal HERIZON-BTC-01 Trial Of Zanidatamab. How satisfactory are the results?

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Q5.

Zanidatamab monotherapy showed cORR of 41.3% and median duration of response of 12.9 months in patients with previously treated HER2-amplified and expressing biliary tract cancers (BTC). How does it compare to presently available treatment choices?

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Q6.

How much use do you see for Zanidatamab in the future? How likely are you to prescribe it to your patients, based on the results to date?

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Q7.

- What is the role of Herceptin/trastuzumab in the current treatment of BTC?  

- Does Zanidatamab appear to be differentiated from Herceptin based on this data?

- Is the concept behind Zanidatamab mechanism of action plausible that hitting multiple domains of HER2 will lead to cross linking and better activity than a traditional antibody with a single HER2 binding site?  How does that work?

- If Herceptin is typically utilized in the first line for patients with HER2 expression, how useful will a 2nd line approval be? Will Zanidatamab find available patients for second line treatment?

- How would you rate your level of excitement about Zanidatamab in HER2 amplified or expressing BTC on a 1 to 10 scale, and why?

- What were your thoughts on the metastatic Gastroesophageal Adenocarcinoma (mGEA) data at ASCO-GI?

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