Throat Cancer Foundation HPV publications - patient review 2021

1. Introduction

This survey is aimed at people who have, or had, throat cancer caused by HPV.

In 2018, the Throat Cancer Foundation charity published a new guide:

HPV and Throat Cancer: Information for patients, their families and loved ones

This guide has been widely distributed to head and neck cancer clinics and been well-received and widely used. The Throat Cancer Foundation is now updating the guide and, as part of the process, is consulting clinicians, other health professionals and patients to make sure that it is as good as it can be.

Whether or not you have seen the guide before now, we would be very grateful if you could take a look and, using this online survey, let us know what you think of it and about any changes you would like to see.

This survey should take no more than 10 minutes to complete and all the data collected will be treated in the strictest confidence.

The closing date for responses is 13 August 2021.

If you would like to contact the guide's editor directly, please email Peter Baker at

Thank you.

The Throat Cancer Foundation.

1. Have you been, or are you now, a patient with throat cancer caused by HPV? *


2. Have you seen before now the guide for patients, their families and loved ones? *


3. How useful do you think the current guide is to patients, their families or loved ones? *


4. Are there any issues that you think should be covered in the guide but which are currently missing? *


5. Are there any questions that you had or have as patient about HPV and throat cancer that you think should be covered in the guide but are currently missing? *


6. Do you think there are any parts of the guide that should be changed, corrected, updated, etc? *


7. Do you think the guide should be produced in any languages besides English? *


8. Do you have any other comments on the guide for patients, their families and loved ones? *

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