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Timing of Surgery in Nonmetastatic Osteosarcoma of the Pelvis and Sacrum

Primary Purpose

Osteosarcoma of Pelvis

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Doxorubicin
Cisplatin
Methotrexate
Ifosfamide
definitive surgery
pre surgical chemotherapy
Sponsored by
Peking University People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteosarcoma of Pelvis focused on measuring osteosarcoma, pelvis, sacrum

Eligibility Criteria

10 Years - 40 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >10 years and <40 years;
  • High-grade nonmetastatic osteosarcoma in pelvis or sacrum;
  • Diagnosis confirmed histologically and reviewed centrally;
  • No evidence of metastatic disease with computed tomography scan of the chest and radionuclide bone scan, or Positron Emission Tomography (PET/CT) within 2 weeks of entry;
  • No prior therapy;
  • Eastern Cooperative Oncology Group performance status 0-1;
  • Life expectancy >3 months;
  • Adequate renal, hepatic, and hemopoietic function;

Exclusion Criteria:

  • Previously treated by chemotherapy or unplanned surgery in other hospital;
  • Have had other kinds of malignant tumors at the same time;
  • Uncontrolled complications, such as diabetes mellitus and so on;
  • Intravascular tumor thrombus on enhanced CT or magnetic resonance (MR);
  • Unresectable disease evaluated by surgeons.

Sites / Locations

  • Peking University People's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Pre surgical Chemotherapy

Immediate Surgery

Arm Description

Immediate pre surgical chemotherapy treated with four drugs including doxorubicin, cisplatin, high-dose methotrexate (MTX) and ifosfamide in eleven weeks, and then definitive surgery followed by adjuvant chemotherapy according to chemotherapy regimen in Peking University People's Hospital(PKUPH).

Immediate definitive surgery, and then post operative chemotherapy based on doxorubicin, cisplatin, high-dose MTX and ifosfamide according to chemotherapy regimen in PKUPH.

Outcomes

Primary Outcome Measures

Overall survival (OS)
Calculated from the date of treatment start until death, whichever comes first.

Secondary Outcome Measures

Progression-free survival (PFS)
Calculated from the date of treatment start until the time of disease progression or death, whichever comes first.
Tumor necrosis rate
The percentage of tumor necrosis calculated in the resected specimen in Arm 2.

Full Information

First Posted
November 26, 2017
Last Updated
August 25, 2018
Sponsor
Peking University People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03360760
Brief Title
Timing of Surgery in Nonmetastatic Osteosarcoma of the Pelvis and Sacrum
Official Title
Presurgical Chemotherapy Compared With Immediate Surgery and Adjuvant Chemotherapy for Nonmetastatic Osteosarcoma of the Pelvis and Sacrum
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
February 2020 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University People's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To study the effect of the timing of surgery on outcome of patients with nonmetastatic osteosarcoma of pelvis and sacrum.
Detailed Description
Successful therapeutic interventions to prevent disease progression in patients with nonmetastatic osteosarcoma of pelvis and sacrum have included surgery with adjuvant chemotherapy. Pre-surgical chemotherapy has been advocated for these patients because of putative improvement in event-free survival (EFS). The advantages of pre-surgical chemotherapy include early administration of systemic chemotherapy, shrinkage of primary tumor, and pathologic identification of risk groups. The theoretic disadvantage is that it exposes a large tumor burden to marginally effective chemotherapy, especially in the axial region. The contribution of chemotherapy and surgery timing has not been tested rigorously. To study the effect of the timing of surgery on outcome of patients with nonmetastatic osteosarcoma of pelvis and sacrum, we conducted multicenter randomized trial to determine whether chemotherapy administered before definitive resection of primary tumors improved EFS and overall survival compared with traditional resection of the primary tumor followed by adjuvant chemotherapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteosarcoma of Pelvis
Keywords
osteosarcoma, pelvis, sacrum

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pre surgical Chemotherapy
Arm Type
Experimental
Arm Description
Immediate pre surgical chemotherapy treated with four drugs including doxorubicin, cisplatin, high-dose methotrexate (MTX) and ifosfamide in eleven weeks, and then definitive surgery followed by adjuvant chemotherapy according to chemotherapy regimen in Peking University People's Hospital(PKUPH).
Arm Title
Immediate Surgery
Arm Type
Other
Arm Description
Immediate definitive surgery, and then post operative chemotherapy based on doxorubicin, cisplatin, high-dose MTX and ifosfamide according to chemotherapy regimen in PKUPH.
Intervention Type
Drug
Intervention Name(s)
Doxorubicin
Other Intervention Name(s)
Adriamycin
Intervention Description
60mg/m^2, in the adjuvant chemotherapy regimen for osteosarcoma in PKUPH
Intervention Type
Drug
Intervention Name(s)
Cisplatin
Other Intervention Name(s)
cisplatinum, platamin
Intervention Description
100mg/m^2, in the adjuvant chemotherapy regimen for osteosarcoma in PKUPH
Intervention Type
Drug
Intervention Name(s)
Methotrexate
Other Intervention Name(s)
HD-MTX
Intervention Description
High dose of methotrexate (8-12g/m^2), in the adjuvant chemotherapy regimen for osteosarcoma in PKUPH
Intervention Type
Drug
Intervention Name(s)
Ifosfamide
Other Intervention Name(s)
ifosphamide
Intervention Description
12g/m^2, in the adjuvant chemotherapy regimen for osteosarcoma in PKUPH
Intervention Type
Procedure
Intervention Name(s)
definitive surgery
Intervention Description
Including limb-sparing procedure and amputation
Intervention Type
Other
Intervention Name(s)
pre surgical chemotherapy
Other Intervention Name(s)
neoadjuvant chemotherapy
Intervention Description
chemotherapy that given before definitive surgery
Primary Outcome Measure Information:
Title
Overall survival (OS)
Description
Calculated from the date of treatment start until death, whichever comes first.
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Progression-free survival (PFS)
Description
Calculated from the date of treatment start until the time of disease progression or death, whichever comes first.
Time Frame
5 years
Title
Tumor necrosis rate
Description
The percentage of tumor necrosis calculated in the resected specimen in Arm 2.
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >10 years and <40 years; High-grade nonmetastatic osteosarcoma in pelvis or sacrum; Diagnosis confirmed histologically and reviewed centrally; No evidence of metastatic disease with computed tomography scan of the chest and radionuclide bone scan, or Positron Emission Tomography (PET/CT) within 2 weeks of entry; No prior therapy; Eastern Cooperative Oncology Group performance status 0-1; Life expectancy >3 months; Adequate renal, hepatic, and hemopoietic function; Exclusion Criteria: Previously treated by chemotherapy or unplanned surgery in other hospital; Have had other kinds of malignant tumors at the same time; Uncontrolled complications, such as diabetes mellitus and so on; Intravascular tumor thrombus on enhanced CT or magnetic resonance (MR); Unresectable disease evaluated by surgeons.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jie Xu, M.D.
Phone
86 15901040835
Email
xujie_pkuph@sina.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xie Lu, M.D.
Phone
86 13401044719
Email
sweetdoctor@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Guo
Organizational Affiliation
Peking University People's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University People's Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100034
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jie Xu, M.D.
Phone
86 15901040835
Email
xujie_pkuph@sina.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Undecided

Learn more about this trial

Timing of Surgery in Nonmetastatic Osteosarcoma of the Pelvis and Sacrum

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