Safety and efficacy of addition of VEGFR and EGFR-family oral small-molecule tyrosine kinase inhibitors to cytotoxic chemotherapy in solid cancers: a systematic …

T Funakoshi, A Latif, MD Galsky - Cancer treatment reviews, 2014 - Elsevier
T Funakoshi, A Latif, MD Galsky
Cancer treatment reviews, 2014Elsevier
Background The approach of combining cytotoxic chemotherapy with oral small molecule
tyrosine kinase inhibitors (TKIs) has been explored in a large number of randomized trials, in
a variety of tumor. We performed a systematic review and meta-analysis to evaluate the
safety and efficacy of this therapeutic approach. Patients and methods PubMed and the
ASCO databases were searched up to March 2013. We included randomized trials in which
the FDA approved vascular endothelial growth factor receptor (VEGFR) or epidermal growth …
Background
The approach of combining cytotoxic chemotherapy with oral small molecule tyrosine kinase inhibitors (TKIs) has been explored in a large number of randomized trials, in a variety of tumor. We performed a systematic review and meta-analysis to evaluate the safety and efficacy of this therapeutic approach.
Patients and methods
PubMed and the ASCO databases were searched up to March 2013. We included randomized trials in which the FDA approved vascular endothelial growth factor receptor (VEGFR) or epidermal growth factor receptor-family (EGFR)-targeted TKI in combination with chemotherapy was compared with chemotherapy alone in patients with any type of solid cancer. The endpoints included safety [fatal adverse events (FAEs), treatment discontinuation, any severe (grade 3 or 4) adverse events (AEs), and individual severe AEs] and efficacy [progression-free survival (PFS), and overall survival (OS)]. The pooled relative risk (RR) or hazard ratio (HR) were calculated.
Results
A total of 16,011 patients from 43 trials were included. Compared with chemotherapy alone, the addition of a TKI significantly increased the risk of FAEs (RR, 1.63; 95% CI, 1.32–2.01), treatment discontinuation (RR, 1.80; 95% CI, 1.58–2.06), and any severe AE (RR, 1.25; 95% CI, 1.16–1.36). The addition of a TKI was associated with a significant improvement in PFS (HR, 0.82; 95% CI, 0.76–0.89), but not OS (HR, 0.99; 95% CI, 0.95–1.03).
Conclusions
It is important for physicians to weigh the risk of toxicity versus the modest PFS benefit associated with chemotherapy plus TKI in patients with solid cancers.
Elsevier