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CompletedNCT00686738Updated Mar 23, 2016

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

An observational study in Osteosarcoma, sponsored by National Cancer Center, Korea. Completed at 1 site in Korea, Republic of. Open to participants aged 5 Years to 40 Years. Per ClinicalTrials.gov, last updated 2016-03-23.

Sponsored by National Cancer Center, Korea · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
20
Ages
5 Years to 40 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Osteosarcoma

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Keywords

  • osteosarcoma
  • transforming growth factor-beta 1
  • nuclear factor-kappa B
  • positron emission tomography/computed tomography
  • magnetic resonance spectroscopy
  • predicting response to neoadjuvant chemotherapy
03

In context

Osteosarcoma

437 studies on the registry are indexed under Osteosarcoma; 116 are open to participants now.

This study's enrollment of 20 is below the median of 100 across 88 observational studies indexed under Osteosarcoma.

Browse Osteosarcoma studies →

Lead sponsor

National Cancer Center, Korea is the lead sponsor of 193 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

osteosarcoma patients hospitalized to National Cancer Center, Korea

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

Exclusion Criteria:

  • Pregnant or lactating women
  • Cardiovascular dysfunction
  • History of previous chemotherapy
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
20 participants (actual)
Biospecimen retention
Samples without dna

Groups and cohorts

  • 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.

06

What researchers measure

Primary outcomes

  1. histopathologic necrosis fractions of surgically removed tumor specimen

    Time frame: 12-17 weeks after starting chemotherapy

07

Study locations

1 site
  • National Cancer Center
    Goyang-si, Gyeonggi, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 23, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00686738
Lead sponsor
National Cancer Center, Korea
Responsible party
Byung-Kiu Park (Head of Center for Pediatric Oncology, National Cancer Center, Korea) — Principal investigator
First posted
May 30, 2008
Start date
Feb 2007
Primary completion
Nov 2012
Completion
Dec 2015
Last update
Mar 23, 2016

Study contacts

Byung-Kiu Park, M.D., Ph.D.
principal investigator · Pediatric Oncology Branch, National Cancer Center, Korea

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.

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