Gastrointestinal stromal tumors (GIST) surgery

The treatment always depends on where the tumor is located, how far it has spread and how aggressively it is growing. Existing genetic alterations - the KIT/PDGFRA genotype - also determine the choice of therapy for GIST. A mutation analysis is a prerequisite for the use of medication. In contrast to many other types of cancer, chemotherapy is not promising here.

Operation comes first

Surgery is the treatment of choice for GIST. The prerequisite is that the tumor is not yet too large, has not yet invaded surrounding tissue and has not yet metastasized. Doctors try to remove the tumor as completely as possible through surgery. Minimally invasive surgery using “keyhole surgery” is sometimes possible for small GISTs. The tumor is removed during a laparoscopy. Otherwise, doctors operate through a larger abdominal incision (laparotomy).

Sometimes they first shrink the tumor with medication to make it easier to operate on. Healthy tissue can then be better protected. This procedure is called “neoadjuvant”. Doctors call all treatments that follow an operation “adjuvant”.

Medication for GIST

After an operation, new drugs can help to reduce the risk of relapse. They can also slow down the progression of cancer in advanced gastrointestinal stromal tumors and metastases. The drugs from the group of tyrosine kinase inhibitors act specifically against certain characteristics and properties of the cancer cells. “Targeted therapy” or “targeted therapy”. Doctors call this treatment “targeted therapy”. However, they only help if a certain mutation status (KIT/PDGFRA) is detectable.

The following active ingredients are used:

  • Imatinib: It acts against a special enzyme of the GIST cells, the so-called receptor tyrosine kinase. Imatinib blocks cell division by binding to the enzyme and preventing the transmission of division signals. Treatment can sometimes delay the cancer for a long time. Imatinib is recommended for patients who have undergone surgery and have a high risk of relapse. Doctors also sometimes use it before an operation to reduce the size of the tumor. Patients take the medication in tablet form. You must not interrupt or stop the therapy, otherwise the cancer will flare up again. Nevertheless, the disease progresses in some patients. One option is to first increase the dose of the medication.
  • Sunitinib: The active substance is used if Imatinib is no longer sufficiently effective or patients cannot tolerate the drug. Sunitinib also attacks the receptor tyrosine kinase, but it also influences other signaling pathways in the cell. It is available in the form of tablets.
  • Regorafenib: The drug can help if sunitinib is no longer sufficiently effective and the disease progresses. It is available as tablets.

Researchers are currently working on further active substances against gastrointestinal stromal tumors and their approval.

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Christian Gutschow, Prof. Dr. med.

Chief Physician, Department of Visceral Surgery and Transplantation

Tel. +41 44 255 97 23
Specialties: Surgery of the upper gastrointestinal tract (upper GI) and endocrine surgery

Diana Vetter, PD Dr. med.

Chief Physician, Department of Visceral Surgery and Transplantation

Tel. +41 43 253 02 34
Specialties: Surgery of the upper gastrointestinal tract, Endocrine surgery

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