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期刊名:Sarcoma

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ISSN:1357-714X

e-ISSN:1369-1643

IF/分区:0.0/

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共收录本刊相关文章索引163条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Chandhanarat Chandhanayingyong,Yuhree Kim,J Robert Staples et al. Chandhanarat Chandhanayingyong et al.
The introduction of cytotoxic chemotherapeutic drugs in the 1970's improved the survival rate of patients with bone sarcomas and allowed limb salvage surgeries. However, since the turn of the century, survival data has plateaued for a subse...
Nicolas Penel,Eric Yaovi Amela,Gauthier Decanter et al. Nicolas Penel et al.
We have reviewed the literature data regarding the spectrum of tumors including solitary fibrous tumor and hemangiopericytoma with special focus on definition of the disease, discussion of the criteria for malignancy, and the key elements o...
Bryan Mitton,Noah Federman Bryan Mitton
Alveolar soft part sarcoma (ASPS) is a very rare soft tissue sarcoma which arises primarily in children and young adults. Despite its unique histology and well-characterized genetic translocation, many questions remain regarding the pathoge...
Alexander B Mohseny,Pancras C W Hogendoorn,Anne-Marie Cleton-Jansen Alexander B Mohseny
High-grade osteosarcoma is an aggressive tumor most commonly affecting adolescents. The early age of onset might suggest genetic predisposition; however, the vast majority of the tumors are sporadic. Early onset, most often lack of a predis...
D Y Kachanov,K V Dobrenkov,R T Abdullaev et al. D Y Kachanov et al.
The aim of the study was to assess the incidence and survival rates of soft tissue sarcomas (STSs) in children 0-14 years of age in Moscow Region, Russian Federation. The database of childhood population-based cancer registry of Moscow Regi...
Steven W Thorpe,Kurt R Weiss,Mark A Goodman et al. Steven W Thorpe et al.
In previous reports, patients with Ewing's sarcoma received radiation therapy (XRT) for definitive local control because metastatic disease and pelvic location were thought to preclude aggressive local treatment. We sought to determine if s...
Lars M Wagner,Teresa A Smolarek,Janos Sumegi et al. Lars M Wagner et al.
Advances in molecular pathology now allow for identification of rare tumor cells in cancer patients. Identification of this minimal residual disease is particularly relevant for Ewing sarcoma, given the potential for recurrence even after c...
Peter Reichardt,Michael Leahy,Xavier Garcia Del Muro et al. Peter Reichardt et al.
The aim of the study was to assess health-related quality of life (HRQoL) among metastatic soft tissue (mSTS) or bone sarcoma (mBS) patients who had attained a favourable response to chemotherapy. We employed the EORTC QLQ-C30, the 3-item C...
Armelle Dufresne,Philippe Cassier,Laure Couraud et al. Armelle Dufresne et al.
Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive mesenchymal tumor that develops in the abdominal cavity of young men adults. Patients typically present with symptoms of abdominal sarcomatosis. Diagnosis is based ...
Daniel C Allison,Scott C Carney,Elke R Ahlmann et al. Daniel C Allison et al.
Four decades ago, specialized chemotherapy regimens turned osteosarcoma, once considered a uniformly fatal disease, into a disease in which a majority of patients survive. Though significant survival gains were made from the 1960s to the 19...