Epigenetic Biomarker for Osteosarcoma
Klíčová slova
Abstraktní
Popis
The investigator want to enroll 100 osteosarcoma participants initially treated in Musculoskeletal Tumor Center of Peking University People's Hospital(PKUPH). All those participants will follow the chemo-protocol for osteosarcoma in PKUPH.8 ml of peripheral blood would be drawed before each cycle of chemotherapy for further analysis. After definitive surgery, participants will need to take 8ml of peripheral blood every 2 months for 6 months. A total of 6 times of blood drawing will need to be done.
In hMe-Seal approach, peripheral blood is collected into EDTA-coated Vacutainers. Plasma is collected from the blood samples after centrifugation at 1 600× g for 10 min at 4 °C and 16 000× g at 10 min at 4 °C. CfDNA is extracted using the Circulating Nucleic Acid Kit(QIAGEN). After that, cfDNA (1-10 ng) is end repaired, 3'-adenylated and ligated to DNA Barcodes using KAPA Hyper Prep Kit (Kapa Biosystems). Ligated DNA is incubated in a solution containing HEPES buffer, UDP-6-N3-Glc and βGT . After that, DBCO-PEG4-biotin is directly added to the reaction mixture. Next, DNA is purified by Micro Bio-Spin 30 Column (Bio-Rad). The purified DNA is incubated with M270 Streptavidin beads (Life Technologies) in specific buffer. The beads are subsequently undergone three 5-min washes each with four kinds of different buffers. All binding and washing are done at room temperature with gentle rotation. Beads are then resuspended in water and amplified with 16 cycles of PCR amplification. The PCR products are purified using AMPure XP beads. Pair-end 38bp sequencing is performed on the NextSeq-500 instrument.
Termíny
Poslední ověření: | 10/31/2017 |
První předloženo: | 11/05/2017 |
Odhadovaná registrace vložena: | 11/05/2017 |
První zveřejnění: | 11/07/2017 |
Poslední aktualizace byla odeslána: | 11/07/2017 |
Poslední aktualizace zveřejněna: | 11/12/2017 |
Aktuální datum zahájení studie: | 08/31/2017 |
Odhadované datum dokončení primární: | 10/29/2018 |
Odhadované datum dokončení studie: | 12/30/2018 |
Stav nebo nemoc
Fáze
Skupiny zbraní
Paže | Intervence / léčba |
---|---|
observation group One group of participants are under observation. This trial has two phase. Phase I: 40 participants will be enrolled. Only if epigenetic cfDNA library has been built, investigators would move on to Phase II. Another 60 participants will be enrolled for further analysis. |
Kritéria způsobilosti
Věky způsobilé ke studiu | 10 Years Na 10 Years |
Pohlaví způsobilá ke studiu | All |
Metoda vzorkování | Non-Probability Sample |
Přijímá zdravé dobrovolníky | Ano |
Kritéria | Inclusion Criteria: - 1) histologically confirmed high-grade osteosarcoma; - 2) older than 10 yrs; - 3) initially treated in Musculoskeletal Tumor Center of Peking University People's Hospital; - 4) Serum samples are available; - 5) completed neo-adjuvant chemotherapy and at least 8 cycles of adjuvant chemotherapy; - 6) expected to live longer than 3 months with Eastern Cooperative Oncology Group performance status of 0 or 1; - 7) acceptable hematologic, hepatic, and renal function. Exclusion Criteria: - 1) Serum samples are not qualified; - 2) Patients who could not complete neo-adjuvant chemotherapy or at least 4-month adjuvant chemotherapy; - 3) lost to follow-up. |
Výsledek
Primární výsledná opatření
1. Histologic response [2 months]
Měření sekundárních výsledků
1. Objective Response Rate [2 months]
2. Progression-free survival [2 years]
3. Overall survival [5 years]