Results 41 to 50 of about 957 (113)

A Systematic Review on the Role of Postoperative Radiotherapy in Pelvic Ewing Sarcoma

open access: yesCancer Medicine, Volume 15, Issue 5, May 2026.
ABSTRACT Ewing Sarcoma of the pelvis has poorer outcomes than other anatomical sites, with complex anatomy often precluding resection with wide margins. The role of postoperative radiotherapy (RT) in improving outcomes remains undefined. A systematic review using Medline, Embase and Cochrane databases (1972–April 2024) evaluated postoperative RT's ...
Angela Hong   +16 more
wiley   +1 more source

Primary Primitive Neuroectodermal Tumor of the Kidney [PDF]

open access: yes, 2000
Primitive neuroectodermal tumor(PNET) is a rare tumor, comprising less than 1% of all soft tissue malignancies arising from the peripheral non-autonomic nervous system.
양승철, 정우희, 한웅규
core  

Primitive Neuroectodermal Tumor of the Lung

open access: yesArchives of Pathology & Laboratory Medicine, 2001
Abstract Primitive neuroectodermal tumors occur most frequently in bone and soft tissue but have been reported in other locations. Primary lung primitive neuroectodermal tumors without pleural or chest wall involvement are extremely rare.
A G, Kahn   +3 more
openaire   +2 more sources

Aggressive Desmoplastic Small Round Cell Tumor in an Adult: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive sarcoma that predominantly affects adolescents and young adults. It is defined by a characteristic chromosomal translocation, t(11;22) (p13;q12), resulting in the EWS–WT1 fusion gene.
Seyed Amir Aledavood   +4 more
wiley   +1 more source

Malignant peripheral primitive neuroectodermal (pPNET) of tongue [PDF]

open access: yes, 2007
Primitive neuroectodermal tumors (PNETs) are relatively rare tumors. Tumors that once would have been diagnosed as Ewing's sarcoma are now often designated as peripheral neuroepithelioma or synonymously PNET.
Aksu, Gorkem   +5 more
core   +3 more sources

Integrating oncolytic adenoviruses into combination cancer therapy: Mechanisms, advances and clinical outlook

open access: yesClinical and Translational Medicine, Volume 16, Issue 5, May 2026.
Oncolytic adenoviruses synergise with chemotherapy, radiotherapy and immunotherapy to enhance anti‐tumour efficacy. Chemotherapy and radiotherapy increase tumour susceptibility and antigen release through DNA damage, while immunotherapy restores T‐cell activity.
Vlad Iova   +4 more
wiley   +1 more source

Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor and Related Tumors [PDF]

open access: yes, 2012
Ewing sarcoma/peripheral primitive neuroectodermal tumor (EWS/pPNET) and other tumors with EWS gene rearrangements encompass a malignant and intermediate neoplasm with a broad anatomic distribution and a wide age range but a predilection for soft tissue ...
Louis P. Dehner   +3 more
core   +1 more source

A Systematic Review of Evidence on the Clinical Effectiveness of Surveillance Imaging in Children With Medulloblastoma and Ependymoma

open access: yesPediatric Blood &Cancer, Volume 73, Issue 4, April 2026.
ABSTRACT Surveillance imaging aims to detect tumour relapse before symptoms develop, but it's unclear whether earlier detection of relapse leads to better outcomes in children and young people (CYP) with medulloblastoma and ependymoma. This systematic review aims to identify relevant literature to determine the efficacy of surveillance magnetic ...
Lucy Shepherd   +3 more
wiley   +1 more source

Supratentorial primitive neuroectodermal tumor in an adult: a case report and review of the literature [PDF]

open access: yes, 2012
Introduction Supratentorial primitive neuroectodermal tumors predominantly occur in children, and are rare in the adult population. Less than 100 cases of supratentorial primitive neuroectodermal tumor have been reported in adults internationally.
Amin Jenny   +20 more
core   +1 more source

NFIB Regulates Chemoresistance in Small Cell Lung Cancer by Suppressing Notch Signaling Activity

open access: yesCancer Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background Small cell lung cancer (SCLC) is an aggressive malignancy characterized by the rapid development of therapy resistance, the underlying mechanisms of which remain incompletely understood. The transcription factor NFIB is a recognized oncogene in SCLC, promoting tumor progression by regulating metastasis and proliferation.
Weixin Qin   +5 more
wiley   +1 more source

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