Long-Term Response to Tyrosine Kinase Inhibitors for Metastatic Renal Cell Carcinoma

Martina Catalano1, Ugo De Giorgi2, Marco Maruzzo3

  • 1Department of Health Sciences, University of Florence, 50134 Florence, Italy.

Biomedicines
|October 27, 2022
PubMed

Insights

Tyrosine kinase inhibitors (TKIs) can lead to long-term responses in metastatic renal cell carcinoma (mRCC) patients. Previous nephrectomy, good performance status, and no liver metastasis are key predictors of these durable responses.

Area of Science:

  • Oncology
  • Medical Research

Background:

  • Metastatic renal cell carcinoma (mRCC) treatment often involves tyrosine kinase inhibitors (TKIs).
  • Some patients achieve long-term progression-free survival (PFS) with TKIs.
  • Identifying predictors of long-term response is crucial for treatment optimization.

Purpose of the Study:

  • To identify clinical and pathological characteristics associated with long-term responses to first-line TKIs in mRCC patients.
  • To evaluate prognostic factors influencing sustained PFS during TKI therapy.

Main Methods:

  • Retrospective review of 335 mRCC patients receiving first-line TKIs (2010-2017).
  • Definition of long-term responders as those progression-free for ≥36 months.
  • Logistic regression analysis to determine predictors of long-term response.

Main Results:

  • Median PFS and overall survival for long-term responders were 70 and 106 months, respectively.
  • Multivariate analysis identified prior nephrectomy, ECOG PS < 1, and absence of liver metastasis as favorable prognostic factors.
  • Specific factors like female gender and ECOG PS < 1 showed differential impact based on risk stratification.

Conclusions:

  • TKIs can induce durable responses in a subset of mRCC patients.
  • Predictors of long-term response include prior nephrectomy, optimal Eastern Cooperative Oncology Group Performance Status (ECOG PS = 0), and lack of liver metastasis.

Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.8K
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
235
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
5.0K
Receptor Tyrosine Kinases01:26

Receptor Tyrosine Kinases

Receptor tyrosine kinases or RTKs are membrane-bound receptors that phosphorylate specific tyrosine on protein substrates. RTKs regulate cellular growth, differentiation, survival, and migration. They contain an extracellular ligand binding domain, a transmembrane domain, and a cytosolic tail with intrinsic kinase activity. Several extracellular signaling molecules activate RTKs in one or more ways and relay the signal downstream. Ligands such as platelet-derived growth factor (PDGF) or...
13.7K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.9K
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
2.7K