Learn about KRAS Mutation Analysis Treatment in Turkey — how it works, who it is for, recovery timelines, and what to expect before and after surgery. Compare hospitals and doctors experienced in KRAS Mutation Analysis and request assistance for cost estimates or appointments.

About KRAS Mutation Analysis

KRAS Mutation Analysis is a specialized genetic test performed by Genetic Medicine specialists to detect specific mutations in the KRAS gene. This gene plays a critical role in cell growth and division. Mutations in KRAS are commonly found in several cancers, most notably colorectal, pancreatic, and non-small cell lung cancer. The analysis is typically performed on a tissue sample obtained from a tumor biopsy or surgical resection. Identifying a KRAS mutation provides crucial information for oncologists, as it can determine a patient's eligibility for targeted therapies, such as EGFR inhibitors, and helps predict treatment response and prognosis. This personalized approach is a cornerstone of modern precision oncology, guiding more effective and tailored treatment plans.

Key Highlights

    Guides personalized, targeted cancer therapy decisions.Helps predict response to specific drugs like EGFR inhibitors.Provides critical prognostic information for several cancer types.Uses advanced molecular techniques for high accuracy.Enables a precision medicine approach to oncology care.

Who is this surgery for?

  • Diagnosis of metastatic colorectal cancer to guide anti-EGFR therapy.
  • Evaluation of advanced non-small cell lung cancer (NSCLC).
  • Diagnosis and management of pancreatic ductal adenocarcinoma.
  • Part of the molecular profiling for various solid tumors.
  • When standard chemotherapy has failed, to identify targeted options.
  • For patients being considered for clinical trials involving KRAS-targeted drugs.

How to prepare

  • Consultation with an oncologist or genetic counselor to discuss the test's purpose.
  • Provision of a formalin-fixed, paraffin-embedded (FFPE) tissue block or slides from a prior biopsy or surgery.
  • If a new biopsy is needed, standard pre-biopsy preparations (like fasting) may apply.
  • Informed consent process explaining the genetic nature of the test.
  • Insurance pre-authorization may be required.

Risks & possible complications

  • Risks are primarily associated with the tissue biopsy procedure (if a new sample is needed), such as bleeding, infection, or pain.
  • Potential for an inconclusive result if the tissue sample has insufficient tumor DNA.
  • Psychological impact of genetic information related to prognosis.
  • Possible insurance or privacy concerns regarding genetic data (handled under strict confidentiality).
  • No direct physical risks from the laboratory analysis itself.

Recovery & hospital stay

  • Recovery is from the biopsy procedure, not the genetic test. Patients can typically resume normal activities shortly after a needle biopsy.
  • Care for the biopsy site as instructed (e.g., keeping it clean and dry).
  • Results are usually available within 7-14 business days and will be discussed in a follow-up appointment with the oncologist.
  • The oncologist will explain the results and their implications for the treatment plan.
  • No specific lifestyle changes are required post-analysis.
  • checked Typical hospital stay: 0 days (outpatient for biopsy if needed)
  • checked Expected recovery time: 0-2 days (from biopsy procedure)

Frequently Asked Questions

If you are considering kras mutation analysis in Turkey, these questions and answers can help you make a confident, informed decision.

Procedure cost in other countries

Here is an overview of how the estimated cost, hospital stay, and recovery time for kras mutation analysis compare across other countries where we have data.

Country Estimated cost range Typical stay Recovery time View details
India USD 87 – USD 272 0 days (outpatient for biopsy if needed) ~ 0-2 days (from biopsy procedure) Know More
Turkey USD 644 – USD 2,013 0 days (outpatient for biopsy if needed) ~ 0-2 days (from biopsy procedure) Know More
PATIENT REVIEW

As a 72-year-old retired botanist with...

As a 72-year-old retired botanist with unexplained neurological decline, I was misdiagnosed for years until Dr. Grace Swarna Priya identified my rare ATXN2 gene mutation. Her personalized management plan at MIOT Hospital has slowed my progression remarkably, I can now enjoy gardening again with adapted tools.