Apatinib+IE
Drugapatinib po; ifosfamide ivgtt ; etoposide ivgtt .
NCT Number: NCT05277480
Apatinib has led to positive responses in the treatment of osteosarcoma refractory to first-line chemotherapy. However, apatinib demonstrates only short-lived activity, and the disease control of musculoskeletal lesions is worse than that of pulmonary lesions. This treatment failure has been partly overcome by the addition of ifosfamide and etoposide (IE). We have ever retrospectively compared the activity of apatinib + IE in relapsed or refractory osteosarcoma in two sarcoma centers in China and concluded that for osteosarcoma with multiple sites of metastasis, apatinib + IE demonstrated clinically meaningful antitumor activity and delayed disease progression in patients with recurrent or refractory osteosarcoma after failure of chemotherapy. However to overcome the influence of other interventions on the outcome, we are currently performing a prospective trial to investigate this combination, from which more accurate data on this treatment strategy are expected.
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Notify Me12 year–65 year
All sexes
Interventional
Phase 2
Peking University People's Hospital, Beijing, Beijing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
apatinib po; ifosfamide ivgtt ; etoposide ivgtt .
ifosfamide ivgtt ; etoposide ivgtt .
Time frame: 2 years
from the start of target treatment until disease progression or death, whichever came first.
Time frame: 3 years
from the date of treatment initiation to death from any cause.
Time frame: 2 years
defined as the proportion of subjects whose best overall response (BOR) is CR or PR, evaluated by investigator based on RECIST v1.1
Time frame: 2 years
defined as the proportion of subjects whose best overall response (BOR) is complete response (CR), partial response (PR) and stable disease (SD), evaluated by investigator based on RECIST v1.1.
Time frame: 2 years
defined as the time from first unconfirmed complete response (CR)/ unconfirmed partial response (PR), evaluated by investigator based on RECIST v1.1, to progressive disease (PD) or any cause of death, whichever occurs first.
Time frame: 2 years
defined as the time from randomization to first CR/PR, evaluated by investigator based on RECIST v1.1.
Time frame: 2 years
defined as the time from randomization to progress disease, evaluated by nvestigator based on RECIST v1.1
Time frame: 2 years
defined as the percentage of patients who were alive and free of disease progression at 4 months evaluated by investigator based on RECIST v1.1
Time frame: 2 years
defined as the percentage of patients who were alive and free of disease progression at 6 months evaluated by investigator based on RECIST v1.1
Peking University People's Hospital
Other
Apatinib in Combination With Ifosfamide and Etoposide (IE) for Relapsed or Refractory Osteosarcoma Progressed Upon First-line Chemotherapy (AIEO): a Prospective, Multiple-centre, Two-arm, Phase 2 Trial
Acronym: OAIE
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