Many tumors have certain characteristics that distinguish them from healthy cells. These may include an increased number of receptors on the cell surface, certain specific mutations, or the activation of certain genes.
This means that these cells have a specific target, which is targeted by specially developed drugs. Identifying these targets requires additional immunohistochemical or genetic testing of the tumor tissue.
The effectiveness of targeted therapy depends on the tumor type and stage of the disease. Overall survival for lung cancer reaches more than 20 months, for kidney cancer – 15-20 months, and for thyroid cancer – up to 2-2.5 years. In the early stages, targeted therapy reduces the risk of cancer recurrence, while in later stages, it enhances the effectiveness of other treatments and prolongs life.
The advantages of targeted therapy include:
The price of a course of targeted therapy depends on several factors:
At the K+31 clinic in Moscow, the cost of targeted therapy corresponds to official price lists, without hidden markups. This provides patients with a treatment plan with transparent pricing, including all necessary procedures and specialist support.
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Targeted therapy in the treatment of breast cancer
In most cases, malignant breast tumors are associated with overexpression of the HER2 surface receptor, which is responsible for adequate cell growth and development. For patients with HER2-associated tumors, adjuvant targeted therapy is indicated (if the tumor is larger than 2 cm and there are lymph node metastases).
Treatment involves medications that specifically target the HER2 receptor. These include intravenous agents such as pertuzumab, emtansine, trastuzumab, and others, as well as oral medications such as apatinib. Due to its precise action, targeted therapy has low toxicity compared to chemotherapy.
Targeted Therapy for Metastatic Lung Cancer
For the treatment of non-small cell metastatic lung cancer, targeted therapy is used alone or in combination with chemotherapy. Oncologists prefer drugs that block angiogenesis, EGFR (epidermal growth factor receptor), ALK (also known as ALK), and BRAF mutations. These drugs include bevacizumab, dabrafenib, erlotinib, crizotinib, and others.
Targeted Therapy for Melanoma
Melanoma is often caused by a pathological change in the BRAF gene, which leads to the production of a rapidly reproducing protein of the same name. BRAF inhibitors, such as vemurafenib, are used in targeted therapy to treat this type of cancer. If a change in the MEK gene is detected during diagnosis, agents that target it (trametinib, etc.) are added to the treatment.
Certain types of melanoma, particularly in areas of skin frequently exposed to ultraviolet radiation, are caused by a mutation in the C-KIT gene. In these cases, nilotinib or imatinib are preferred.
Targeted Therapy for Pancreatic Cancer
Pancreatic cancer is caused by the following mutations: SMAD4, BRCA, TP53, KRAS, and CDKN2A. There are targeted therapy drugs that specifically target these mutations, such as erlotinib. Treatment often uses a mixed approach in combination with chemotherapy. Research at Johns Hopkins University has shown that targeted therapy helps prolong the lives of people seeking treatment in the advanced stages of cancer.
Targeted Therapy for Colorectal Cancer
This anticancer treatment method is chosen for patients with metastases. The main drugs used include:
Targeted Therapy for Stomach Cancer
Stomach cancer is a common type of gastrointestinal cancer. It is the second-leading cause of death among all cancers. Targeted therapy for its treatment includes three drugs:
Targeted Therapy for Kidney Cancer
Targeted therapies for kidney cancer aim to block the growth of blood vessels that feed the tumor, halt cell division, and prevent metastasis. These include:
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