Development of Indices Predicting Response to Pre-operative Chemotherapy in Osteosarcoma Patients

NCT ID: NCT00686738

Last Updated: 2016-03-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-02-28

Study Completion Date

2015-12-31

Brief Summary

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The purpose of this study is to develop indices predicting response to pre-operative chemotherapy in osteosarcoma patients. Histologic response to pre-operative chemotherapy is very important for the ultimate outcome of osteosarcoma patients. Conventional methods such as CT or MRI evaluating tumor response to chemotherapy is not so efficient in tumors like osteosarcoma. Instead, the investigators will test whether blood TGF-b1 levels, PET/CT findings, MRS findings as well as the level of NF-kB expression in tumor tissues can predict chemotherapy response in osteosarcoma.

Detailed Description

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We will conduct a prospective trial to verify the validity of indices utilizing TGF-b1, NF-kB, PET/CT, and MRS for predicting response to neoadjuvant chemotherapy in osteosarcoma patients. We assume that changes in plasma TGF-b1 levels, PET/CT and magnetic resonance spectroscopy (MRS) findings during the period of neoadjuvant chemotherapy as well as the initial nuclear NF-kB expression status of tumor biopsy specimen either alone or in combination may predict a chemotherapeutic response determined by histopathologic necrosis fractions of tumors removed. To test this, we will obtain TGF-b1 levels, PET/CT and MRS findings at diagnosis and at follow-up (after first and second/third chemotherapy cycle). Tumor will then be removed. Chemotherapy regimen comprised of various combination of cisplatin, adriamycin, and high-dose methotrexate, ifosfamide, and etoposide. Indices derived from TGF-b1, PET/CT, MRS predicting greater than 90% necrosis fractions will be sought utilizing statistical methods.

Conditions

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Osteosarcoma

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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A

Study group will be made up of patients hospitalized to National Cancer Center, Korea, aged between 5 and 40 years, and diagnosed with high grade osteosarcoma by histological exam.

In this group, TGF-b1 measurement, PET/CT and MRS examination at diagnosis, after 1st cycle chemotherapy, and 2nd or 3rd chemotherapy (just before surgery) will be made.

In addition, evaluation of NF-kB expression status in tumor specimens at diagnostic biopsy and tumor removing surgery will be done.

The results of above studies will be correlated with the necrosis fractions of the tumor tissues removed by surgery.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Karnofsky (over 15 years) or Lansky (less than 15 years) score equal or greater than 50
* Adequate organ functions:

* GFR\>60ml/min/1.73m2
* EF\>50% or SF\>28% on echocardiogram
* ANC\>1.5 x 10\^9/L
* platelet\>100 x 10\^9/L
* Obtainment of informed consents from parents/legal guardians and/or patients

Exclusion Criteria

* Pregnant or lactating women
* Cardiovascular dysfunction
* History of previous chemotherapy
Minimum Eligible Age

5 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Center, Korea

OTHER_GOV

Sponsor Role lead

Responsible Party

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Byung-Kiu Park

Head of Center for Pediatric Oncology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Byung-Kiu Park, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Pediatric Oncology Branch, National Cancer Center, Korea

Locations

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National Cancer Center

Goyang-si, Gyeonggi-do, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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NCCCTS-07-256

Identifier Type: -

Identifier Source: org_study_id

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