Literature DB >> 19662473

Multiinstitutional phase II study of neoadjuvant chemotherapy for osteosarcoma (NECO study) in Japan: NECO-93J and NECO-95J.

Yukihide Iwamoto1, Kazuhiro Tanaka, Kazuo Isu, Akira Kawai, Shin-ichiro Tatezaki, Takeshi Ishii, Kazuyoshi Kushida, Yasuo Beppu, Masamichi Usui, Akio Tateishi, Kiyoo Furuse, Takeshi Minamizaki, Noriyoshi Kawaguchi, Shinya Yamawaki.   

Abstract

BACKGROUND: Osteosarcoma is the most frequent primary malignant bone tumor. In Europe and the United States, its prognosis has been greatly improved by the use of multimodal treatment, including preoperative and postoperative chemotherapy as well as surgery. In Japan, however, only a few clinical studies on osteosarcoma have been carried out.
METHODS: To evaluate the efficacy of neoadjuvant chemotherapy on nonmetastatic, operable osteosarcoma arising in the extremities, a prospective multi-institutional phase II trial, the Neoadjuvant Chemotherapy for Osteosarcoma (NECO) study, was conducted. Preoperative chemotherapy included high-dose methotrexate (HD-MTX), cisplatin (CDDP), and adriamycin (ADR). If the induction therapy was assessed as not effective, high-dose ifosfamide (IFO) was added to the chemotherapy regimen. A total of 124 patients were enrolled in this trial, and ultimately 113 patients were eligible.
RESULTS: The 5-year overall survival (OAS) and event-free survival (EFS) rates in the NECO study were 77.9% and 65.5%, respectively. A good histological response to the induction chemotherapy resulted in favorable OAS (78.7%). The patients assessed as poor histological responders with progressive disease after the induction chemotherapy exhibited comparable outcomes (OAS 89.5%, EFS 68.2%). There were no significant differences between the OAS and EFS rates of the patients in terms of response to preoperative chemotherapy.
CONCLUSIONS: We analyzed the results of the intensive neoadjuvant chemotherapy and the effects of adding IFO on patients with osteosarcoma in Japan. The results suggest efficacy of the high-dose IFO addition to the standard three-drug chemotherapy regimen. However, a randomized clinical study is needed to establish the true impact of IFO on patients with osteosarcoma.

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Year:  2009        PMID: 19662473     DOI: 10.1007/s00776-009-1347-6

Source DB:  PubMed          Journal:  J Orthop Sci        ISSN: 0949-2658            Impact factor:   1.601


  43 in total

1.  S-phase kinase-associated protein 2 promotes cell growth and motility in osteosarcoma cells.

Authors:  Lu Ding; Rong Li; Rongxin Sun; Yang Zhou; Yubo Zhou; Xiaoping Han; Yong Cui; Wu Wang; Qing Lv; Jingping Bai
Journal:  Cell Cycle       Date:  2017-08-03       Impact factor: 4.534

2.  Pulsed Electromagnetic Field Stimulation Promotes Anti-cell Proliferative Activity in Doxorubicin-treated Mouse Osteosarcoma Cells.

Authors:  Yoshitaka Muramatsu; Takuya Matsui; Masataka Deie; Keiji Sato
Journal:  In Vivo       Date:  2017-01-02       Impact factor: 2.155

3.  Intensified Chemotherapy With Dexrazoxane Cardioprotection in Newly Diagnosed Nonmetastatic Osteosarcoma: A Report From the Children's Oncology Group.

Authors:  Cindy L Schwartz; Leonard H Wexler; Mark D Krailo; Lisa A Teot; Meenakshi Devidas; Laurel J Steinherz; Allen M Goorin; Mark C Gebhardt; John H Healey; Judith K Sato; Paul A Meyers; Holcombe E Grier; Mark L Bernstein; Steven E Lipshultz
Journal:  Pediatr Blood Cancer       Date:  2015-09-23       Impact factor: 3.167

4.  Cell division cycle 20 promotes cell proliferation and invasion and inhibits apoptosis in osteosarcoma cells.

Authors:  Guanning Shang; Xu Ma; Gang Lv
Journal:  Cell Cycle       Date:  2017-12-22       Impact factor: 4.534

5.  Fatty acid synthase expression in osteosarcoma and its correlation with pulmonary metastasis.

Authors:  Zhi Li Liu; Gao Wang; Ai Fen Peng; Qing Feng Luo; Yang Zhou; Shan Hu Huang
Journal:  Oncol Lett       Date:  2012-08-14       Impact factor: 2.967

6.  The relation of tumour necrosis and survival in patients with osteosarcoma.

Authors:  Xin Li; Adedayo O Ashana; Vincent M Moretti; Richard D Lackman
Journal:  Int Orthop       Date:  2011-02-26       Impact factor: 3.075

7.  Elevated Expression of Transforming Acidic Coiled-Coil Containing Protein 3 (TACC3) Is Associated With a Poor Prognosis in Osteosarcoma.

Authors:  Kotaro Matsuda; Hiroaki Miyoshi; Koji Hiraoka; Tetsuya Hamada; Kazutaka Nakashima; Naoto Shiba; Koichi Ohshima
Journal:  Clin Orthop Relat Res       Date:  2018-09       Impact factor: 4.176

8.  Vitronectin significantly influences prognosis in osteosarcoma.

Authors:  Kai Shi; Rui-Long Lan; Xuan Tao; Chao-Yang Wu; Hai-Feng Hong; Jian-Hua Lin
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

9.  Sunitinib malate (SU-11248) reduces tumour burden and lung metastasis in an intratibial human xenograft osteosarcoma mouse model.

Authors:  Ram Mohan Ram Kumar; Matthias Je Arlt; Aleksandar Kuzmanov; Walter Born; Bruno Fuchs
Journal:  Am J Cancer Res       Date:  2015-06-15       Impact factor: 6.166

10.  Telomerase-specific oncolytic immunotherapy for promoting efficacy of PD-1 blockade in osteosarcoma.

Authors:  Yusuke Mochizuki; Hiroshi Tazawa; Koji Demiya; Miho Kure; Hiroya Kondo; Tadashi Komatsubara; Kazuhisa Sugiu; Joe Hasei; Aki Yoshida; Toshiyuki Kunisada; Yasuo Urata; Shunsuke Kagawa; Toshifumi Ozaki; Toshiyoshi Fujiwara
Journal:  Cancer Immunol Immunother       Date:  2020-11-05       Impact factor: 6.968

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