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NCT05277480CompletedPhase 2

Apatinib With Ifosfamide Plus Etoposide for Relapsed or Refractory Osteosarcoma (OAIE)

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

Source: ClinicalTrials.gov · Last updated 31 Jul 2024

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
81 (actual)
First submitted
3 Mar 2022
Start date
1 Mar 2022
Primary completion date
30 Jun 2023
Lead sponsor
Peking University People's Hospital
NCT number
NCT05277480

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 81
  • From 1 Mar 2022 to the primary completion date, 30 Jun 2023
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • those who had been previously treated with antiangiogenic TKIs and single IE chemotherapy;
  • all patients were assessed by the sarcoma board including a thoracic surgeon with at least 10 years surgical experience. Patients with lung metastases only were carefully assessed for eligibility for metastasectomy, of whom those who were suitable for surgery were excluded from this study;
  • surgical procedure or radiotherapy within 4 weeks of enrollment;
  • activegastroduodenal ulcer, previous condition associated with risk of bleeding or requiring anticoagulation;

Other illness

  • weight loss of 20% or more before illness;
  • women who were pregnant or breast feeding, other malignancy;
  • positive HBV/HCV/HIV serology, and known allergy to the experimental agents.

Lab values

  • those who had severe or uncontrolled medical disorders that could jeopardize the outcomes of the study. These confounding conditions included, cardiac clinical symptoms or disease with left ventricular ejection fraction\<50%, and hypertension that could not be well controlled with antihypertensive drugs.;
  • proteinuria or hematuria, denutrition with albuminemia \<25 g/L;

Other

  • brain or leptomeningeal metastasis;

Who the study is looking for

  • advanced recurrent and refractory osteosarcoma confirmed by histopathology;
  • initial treatment in the Orthopedic/Oncology Departments of Peking University People's Hospital or Peking University Shougang Hospital;
  • progression less than 6 months after first-line chemotherapy with a combination of high-dose methotrexate, doxorubicin, cisplatin and ifosfamide (first-line chemotherapy);
  • measurable lesions according to the Response Evaluation Criteria for Solid Tumors (RECIST 1.1) ;
  • Eastern Cooperative Oncology Group performance status ≤ 1 ;
  • acceptable haematologic, hepatic, and renal function.

Age in the registry: 12 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University
Coordinator of this site? Confirm its status
NanjingChinaUnknown status
Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.