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Information on how to access Mylotarg™​​​​​​​​​​​​​​ (gemtuzumab ozogamicin) and cytarabine prescribing information and adverse event reporting can be found at the bottom of the page.

AML Landscape: Present and Future Video

Speaker: Dr Eleni Tholouli

Duration: 02.23

In this video, Dr. Tholouli discusses Mylotarg’s NICE approval and its practical approach to the issue of waiting for cytogenics and Mylotarg’s use1. Dr Tholouli also mentions results in event free survival and relapse risk alongside the safety data2. Practical considerations using the ALFA schedule, platelet recovery, risk of VOD and minimising risks to the liver are also considered2.

Dr. Eleni Tholouli is a Consultant Haematologist at Manchester University NHS Trust and Director of the Adult Stem Cell Transplant Unit. She is a member of the Haemato-Oncology Pathway Board at Manchester Cancer and of national bodies such as the AML Working Group and the Blood and Marrow Transplantation Clinical Reference Group. Her expertise covers a wide range of haemato-oncological malignancies and non-malignant disorders.

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Efficacy and Safety of MYLOTARG video

Watch Professor Robert Hills discuss the key clinical data from the pivotal ALFA study

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Fast Facts

Download the Fast Facts PDF document to aid your understanding of MYLOTARG

View Fast Facts PDF

AML, Acute Myeloid Leukaemia

▼ 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. See section 4.8 of the SmPC for how to report adverse reactions.
References:
  1. NICE Technology Appraisal Guidance (TA545). Gemtuzumab ozogamicin for untreated acute myeloid leukaemia. Available at: https://www.nice.org.uk/guidance/TA545/history. Published: 14 November 2018. Accessed March 2021.
  2. MYLOTARG Summary of Product Characteristics. Available at: https://www.medicines.org.uk/emc/product/9151/smpc. Accessed March 2021.
PP-MYL-GBR-0238. March 2021

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