Renal Cell Cancer Clinical Trial
Official title:
Fecal Microbiota Transplantation to Treat Diarrhea Induced by Tyrosine-kinase Inhibitors in Patients With Metastatic Renal Cell Carcinoma: a Randomized Clinical Trial.
Tyrosine kinase inhibitors (TKIs) have improved the survival of patients with metastatic renal cell carcinoma, and are commonly used as first-line option for this condition, but their use is encumbered by side effects, mainly diarrhea, for which there are no standardized strategies. Increasing evidence suggests that gut microbiota could influence the development of TKIs-induced diarrhea. In theory, the therapeutic modulation of gut microbiota could be an approach to alleviate TKI-induced diarrhea. Fecal microbiota transplantation (FMT) is the infusion of fecal microbiota from a healthy donor in the gut of a recipient with the aim of curing a specific disease. It has been increasingly recognized as a highly effective treatment against recurrent Clostridium difficile infection.To date, the effects of FMT on chemotherapy-related diarrhea are unknown. This study will evaluate, through a randomized controlled design, the efficacy of fecal microbiota transplantation (FMT), compared with sham FMT, in treating TKI-induced diarrhea in patients with metastatic renal cell carcinoma.
Despite the improvement in diagnosis and management, renal cell carcinoma (RCC) remains one
of the most burdensome urological cancers, being the sixth most common malignancy in men and
the 10th in women, accounting, respectively, for 5% and 3% of all cancers. Moreover, the
incidence of RCC is increasing, especially in Western countries, accounting for nearly 60000
new cases per year in the United States. A considerable proportion of patients present with
metastatic disease at diagnosis, and there are more than 140000 RCC-dependent deaths per year
worldwide according to the World Health Organization.
Sunitinib and pazopanib are oral multi-targeted receptor tyrosine kinase inhibitors (TKIs)
that have dramatically improved the survival of patients with metastatic RCC, and are
commonly used as first-line option for this condition.
However, long-term use of these drugs is prevented by the development of toxicity. Diarrhea
is one of the most common side effects of TKIs, occurring in nearly 50% of patients. It
decreases the quality of life of these patients, and often requires dose reduction and drug
discontinuation, potentially decreasing the efficacy of TKIs.
To date there are no standardized strategies for TKIs-related diarrhea, and current
recommendations are supported by few evidence or real-life experience. Recommended treatment
options include anti-motility agents, which are not targeted to act on the pathogenic
pathways of diarrhea.
Increasing evidence suggests that gut microbiota could influence the development of
TKIs-induced diarrhea. Overall, chemotherapy is known to drive, through the development of
mucositis, deep compositional and functional alterations of gut microbiota. Mucositis occurs
commonly after treatment with TKIs, and a specific dysbiotic profile has been found in
patients with TKIs-induced diarrhea.
In theory, the therapeutic modulation of gut microbiota could be an approach to alleviate
TKI-induced diarrhea. Although probiotics have been suggested as a possible treatment option
for this condition, few evidence supports this indication.
Fecal microbiota transplantation (FMT) is the infusion of fecal microbiota from a healthy
donor in the gut of a recipient with the aim of curing a specific disease. It has been
increasingly recognized as a highly effective treatment against recurrent Clostridium
difficile infection.
FMT has been also examined as a potential approach for other disorders associated with a
disruption of gut microbiota, including ulcerative colitis or metabolic syndrome.
To date, the effects of FMT on chemotherapy-related diarrhea are unknown. The aim of this
study is to investigate the efficacy of fecal microbiota transplantation (FMT), compared with
sham FMT, in treating TKI-induced diarrhea in patients with metastatic RCC
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