From 1 August 2021, patients with unresectable or metastatic bowel cancer (mCRC) that is mismatch repair deficient (dMMR) will have a new treatment option, with the subsidised listing of Keytruda on the Pharmaceutical Benefits Scheme (PBS). Keytruda works to reactivate the immune system to detect and attack tumour cells and is the first subsidised immunotherapy for bowel cancer patients. No longer will patients and their families be faced with the decision of whether to go into debt to fund the treatment or to decline it. ++++++ Patients with BRAF V600E-variant metastatic bowel cancer are one step closer to accessing a subsidised third-line treatment option, following a positive recommendation by the Pharmaceutical Benefits Advisory Committee (PBAC) to list Braftovi in combination with Erbitux. Until listing on the PBS occurs, the treatment is available through the manufacturer’s patient cost-sharing program. “Fortunately, Braftovi gave me all I could hope for; I had very few side effects, and it was much kinder on my body than the chemotherapies I have endured,” said Tuula who was first diagnosed with bowel cancer just over seven years ago at age 67 and began treatment with Braftovi in November 2019. +++++ Avastin was withdrawn from the PBS on 1 June 2021, resulting in forced-switching to the newly listed biosimilar, Mvasi, for patients receiving Avastin unless they paid privately to continue with the biologic. Bowel Cancer Australia remains concerned about how this PBS decision was made, the lack of transparency, and that patients were the last to know. The withdrawal of Avastin signals an erosion of patient choice, despite the Department of Health stating “biosimilar medicines give patients access to more brand options”. |