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Diarrhea Induced by Small Molecule Tyrosine Kinase Inhibitors Compared With Chemotherapy: Potential Role of the
Kate R Secombe1, Ysabella Z A Van Sebille2, Bronwen J Mayo3
1Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia.
Abstract:
Small molecule receptor tyrosine kinase inhibitors (SM-TKIs) are among a group of targeted cancer therapies, intended to be more specific to cancer cells compared with treatments, such as chemotherapy, hence reducing adverse events. Unfortunately, many patients report high levels of diarrhea, the pathogenesis of which remains under investigation. In this article, we compare the current state of knowledge of the pathogenesis of chemotherapy-induced diarrhea (CID) in comparison to SM-TKI-induced diarrhea, and investigate how a similar research approach in both areas may be beneficial. To this end, we review evidence that both treatment modalities may interact with the gut microbiome, and as such the microbiome should be investigated for its ability to reduce the risk of diarrhea.
Insights
Small molecule receptor tyrosine kinase inhibitors (SM-TKIs) can cause diarrhea. Research suggests the gut microbiome may play a role in mitigating this side effect, warranting further investigation.
Area of Science:
- Oncology
- Gastroenterology
- Microbiome Research
Background:
- Small molecule receptor tyrosine kinase inhibitors (SM-TKIs) are targeted cancer therapies with potentially fewer side effects than chemotherapy.
- Diarrhea is a common and significant adverse event in patients treated with SM-TKIs, with its pathogenesis not fully understood.
- Chemotherapy-induced diarrhea (CID) is a well-studied condition, offering a potential model for understanding SM-TKI-induced diarrhea.
Purpose of the Study:
- To compare the current understanding of the pathogenesis of chemotherapy-induced diarrhea (CID) and SM-TKI-induced diarrhea.
- To explore how similar research methodologies applied to both types of diarrhea could yield beneficial insights.
- To investigate the potential role of the gut microbiome in the development of SM-TKI-induced diarrhea.
Main Methods:
- Literature review comparing existing knowledge on CID and SM-TKI-induced diarrhea.
- Analysis of evidence regarding the interaction between cancer therapies and the gut microbiome.
- Comparative analysis of research approaches for studying treatment-induced gastrointestinal toxicities.
Main Results:
- Both chemotherapy and SM-TKIs show potential interactions with the gut microbiome.
- Evidence suggests the gut microbiome's composition and function may influence the risk and severity of treatment-induced diarrhea.
- A unified research approach may accelerate understanding of these complex interactions.
Conclusions:
- The gut microbiome is a promising area for investigation in the context of SM-TKI-induced diarrhea.
- Understanding microbiome-therapy interactions could lead to novel strategies for preventing or managing diarrhea in cancer patients.
- Further research into the gut microbiome's role is crucial for improving patient outcomes and reducing adverse events associated with targeted cancer therapies.
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