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期刊名:Clinical sarcoma research

缩写:CLIN SARCOMA RES

ISSN:2045-3329

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IF/分区:0.0/

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共收录本刊相关文章索引197
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
Dagmar Berghuis,Marco W Schilham,Hanneke I Vos et al. Dagmar Berghuis et al.
Background: Ewing sarcoma patients have a poor prognosis despite multimodal therapy. Integration of combination immunotherapeutic strategies into first-/second-line regimens represents promising treatment options, particu...
Annmeik M van Maldegem,Pancras Cw Hogendoorn,Andrew B Hassan Annmeik M van Maldegem
Ewing Sarcoma is the second most common primary bone sarcoma with 900 new diagnoses per year in Europe (EU27). It has a poor survival rate in the face of metastatic disease, with no more than 10% survival of the 35% who develop recurrence. ...
Fergal C Kelleher,David M Thomas Fergal C Kelleher
Background: Ewing sarcoma/PNET is managed with treatment paradigms involving combinations of chemotherapy, surgery, and sometimes radiation. Although the 5-year survival rate of non-metastatic disease approaches 70%, thos...
Annemiek M van Maldegem,Aparna Bhosale,Hans J Gelderblom et al. Annemiek M van Maldegem et al.
Background: High grade primary bone sarcomas are rare cancers that affect mostly children and young adults. Osteosarcoma and Ewing sarcoma are the most common histological subtypes in this age group, with current multimod...
Emanuela Palmerini,Marco Gambarotti,Eric L Staals et al. Emanuela Palmerini et al.
Background: Dermatofibrosarcoma protuberans (DFSP) is a relatively common soft-tissue tumor. A more aggressive appearing fibrosarcoma may arise in DFSP, changing its biological behavior. CD34 and apolipoprotein-D are high...
Vincent Pm Cliteur,Károly Szuhai,Hans J Baelde et al. Vincent Pm Cliteur et al.
Desmoplastic small round cell tumour is a rare malignant tumour with a male to female ratio of 4:1. It manifests mostly at serosal sites. Here we present a case of a 28-year-old male patient, who presented with a fast growing paratesticular...
Daniela Katz,Piyaporn Boonsirikamchai,Haeson Choi et al. Daniela Katz et al.
Background: Myxoid liposarcoma (MLS) is a soft tissue sarcoma with adipocytic differentiation characterized by a unique chromosome rearrangement, t(12;16)(q13;p11). The exact efficacy of chemotherapy in MLS has not been c...