Literature DB >> 16860938

Primary bone osteosarcoma in the pediatric age: state of the art.

Alessandra Longhi1, Costantino Errani, Massimiliano De Paolis, Mario Mercuri, Gaetano Bacci.   

Abstract

The current combination treatment, chemotherapy and surgery, has significantly improved the cure rate and the survival rate of primary bone osteosarcoma. The 5-year survival rate has increased in the last 30 years from 10% to 70%. Even in patients with poor prognosis, such as those with metastases at diagnosis, the 5-year survival rate has reached 20-30% due to chemotherapy and the surgical removal of metastases and primary tumor. However, the most effective drugs are still the same as those employed over the last 20 years as front line neoadjuvant or adjuvant chemotherapy: Doxorubicin, Cisplatin, Methotrexate, Ifosfamide. No standard, second line therapy exists for those who relapse. At relapse, due to the lack of new non-cross-resistant drugs, surgery is still the main option when feasible. Other drugs have been employed in relapsed patients with poor results. This article reviews the state of the art of treatment for bone osteosarcoma in the pediatric age.

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Year:  2006        PMID: 16860938     DOI: 10.1016/j.ctrv.2006.05.005

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  232 in total

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2.  Frequent attenuation of the WWOX tumor suppressor in osteosarcoma is associated with increased tumorigenicity and aberrant RUNX2 expression.

Authors:  Kyle C Kurek; Sara Del Mare; Zaidoun Salah; Suhaib Abdeen; Hussain Sadiq; Suk-Hee Lee; Eugenio Gaudio; Nicola Zanesi; Kevin B Jones; Barry DeYoung; Gail Amir; Mark Gebhardt; Matthew Warman; Gary S Stein; Janet L Stein; Jane B Lian; Rami I Aqeilan
Journal:  Cancer Res       Date:  2010-06-08       Impact factor: 12.701

3.  Correlation of non-mass-like abnormal MR signal intensity with pathological findings surrounding pediatric osteosarcoma and Ewing's sarcoma.

Authors:  Karim Z Masrouha; Khaled M Musallam; Alexis Bou Samra; Ayman Tawil; Rachid Haidar; Zaher Chakhachiro; Said Saghieh; Abeer Abdallah; Raya Saab; Samar Muwakkit; Miguel R Abboud; Nabil J Khoury
Journal:  Skeletal Radiol       Date:  2012-03-10       Impact factor: 2.199

4.  CANCER STEM CELLS IN OSTEOSARCOMA.

Authors:  Lindsay Bashur; Guang Zhou
Journal:  Case Orthop J       Date:  2013

5.  microRNA-363 plays a tumor suppressive role in osteosarcoma by directly targeting MAP2K4.

Authors:  Xueqin Li; Xinsheng Liu; Jun Fang; Huazhuang Li; Jingchun Chen
Journal:  Int J Clin Exp Med       Date:  2015-11-15

6.  MicroRNA-192 inhibits the proliferation, migration and invasion of osteosarcoma cells and promotes apoptosis by targeting matrix metalloproteinase-11.

Authors:  Guowei Shang; Yang Mi; Yingwu Mei; Guanghui Wang; Yadong Wang; Xinjie Li; Yisheng Wang; Yuebai Li; Guoqiang Zhao
Journal:  Oncol Lett       Date:  2018-03-12       Impact factor: 2.967

7.  A polysaccharide from Trametes robiniophila Murrill induces apoptosis through intrinsic mitochondrial pathway in human osteosarcoma (U-2 OS) cells.

Authors:  Xingkai Zhao; Shuo Ma; Ning Liu; Jiakun Liu; Wenbo Wang
Journal:  Tumour Biol       Date:  2015-02-11

Review 8.  Specific tyrosine kinase inhibitors regulate human osteosarcoma cells in vitro.

Authors:  Patrick J Messerschmitt; Ashley N Rettew; Robert E Brookover; Ryan M Garcia; Patrick J Getty; Edward M Greenfield
Journal:  Clin Orthop Relat Res       Date:  2008-07-08       Impact factor: 4.176

9.  A novel antisense long non-coding RNA SATB2-AS1 overexpresses in osteosarcoma and increases cell proliferation and growth.

Authors:  Si-Hong Liu; Jian-Wei Zhu; Hui-Hua Xu; Gui-Qiang Zhang; Yan Wang; Ya-Min Liu; Jun-Bo Liang; Yu-Xuan Wang; Yong Wu; Qi-Feng Guo
Journal:  Mol Cell Biochem       Date:  2017-02-11       Impact factor: 3.396

10.  Programmed cell death 2 functions as a tumor suppressor in osteosarcoma.

Authors:  Yuanxun Yang; Yan Jin; Wenxi Du
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01
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