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Prescribing Information

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PHESGO Expert Exchange

PHESGO Expert Exchange is a promotional video series produced by Roche in collaboration with Breast Oncologists. Designed to bring expert’s insights on trial data and PHESGO in clinical practice with real world patients case studies. Watch the videos below to hear Oncologists Dr Mukesh & Dr Okines discuss PHESGO and its impact on UK clinical practice. Always refer to the PHESGO Summary of Product Characteristics (UK) before treating a patient.

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Listen to Dr Okines & Dr Mukesh discuss the treatment of older patients with HER2+ N+ eBC with a real patient case exploring PHESGO in the neoadjuvant setting.

If viewing on mobile, for best viewing experience please rotate your phone to landscape mode.

Listen to Dr Okines & Dr Mukesh discuss key neoadjuvant trial data for pertuzumab/trastuzumab, explore PHESGO neoadjuvant treatment principles for HER2+ early breast cancer, and discuss how to treat patients with residual invasive disease.

Abbreviations: N+: node-positive; eBC: early breast cancer; HER2: human epidermal growth factor receptor 2

PHESGO in the Adjuvant Setting: Hear from your peers

Early breast cancer (eBC)

PHESGO is indicated for use in combination with chemotherapy in:

  • the neoadjuvant treatment of adult patients with HER2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrence1

  • the adjuvant treatment of adult patients with HER2-positive early breast cancer at high risk of recurrence1

The Experts

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Product
Watch how to prepare PHESGO for SC administration

PHESGO is a fixed-dose combination of pertuzumab and trastuzumab in one vial for subcutaneous use given every 3 weeks1

In patients receiving a taxane, PHESGO should be administered prior to the taxane.

 

Patients should be observed for injection-related reactions and hypersensitivity reactions. Observation period should start following administration of PHESGO and be completed prior to any subsequent administration of chemotherapy1

 

 

Once pertuzumab-based therapy has been safely established, the physician may determine the suitability of administration of PHESGO outside of the clinical setting (e.g., at home) by a healthcare professional (see SmPC section 4.4).1

 

Prefer to talk things through? We’re here to speak with you about supporting your HER2+ eBC patients

Connect with our team

nikhita.govind@roche.com
vic.wallace@roche.com
jo.mccarthy@roche.com
john.danks@roche.com
suki.mahal@roche.com
gaby.roe@roche.com
dare.rotimi@roche.com
alan.young.ay2@roche.com
douglas.gibson@roche.com

Reference:

  1. PHESGO Summary of Product Characteristics. Available at: www.medicines.org.uk/emc/product/11989/smpc
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. You can also report via the free Yellow Card app available from the Apple App Store or Google Play Store. Adverse events should also be reported to Roche Products Ltd. 
Please contact Roche Drug Safety Centre by emailing welwyn.uk_dsc@roche.com or calling +44 (0)1707 367554.

Adverse reactions should be reported by brand name and batch number.
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