The purpose of this study is to assess the efficacy and safety of patients who receive apatinib plus docetaxel and zoledronic versus docetaxel and zoledronic alone as second line treatment for advanced non-squamous non-small cell lung cancer with bone metastases.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
apatinib 500 mg qd p.o.docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent
docetaxel 60mg/m² iv q3w;zoledronic 4mg iv\>15min q4w until disease progression or intolerable toxicity or patients withdrawal of consent
Affiliated Hospital of Hebei university
Baoding, Hebei, China
RECRUITINGProgression free survival
Time frame: evaluation per 2 cycles (6 weeks)
Overall survival
Time frame: evaluation per 2 cycles (6 weeks)
DCR (Disease control rate)
Time frame: evaluation per 2 cycles (6 weeks)
ORR (Objective response rate)
Time frame: evaluation per 2 cycles (6 weeks)
SREs(Skeletal-related events)
measured pain, a fracture, the need for bone radiation or surgical therapy, spinal cord compression, or hypercalcemia
Time frame: evaluation per 2 cycles (6 weeks)
Toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0
Time frame: evaluation per 2 cycles (6 weeks)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.