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- Academic Journals (359)
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Academic Journals
- 359
- Search Terms:ISSN: 1357714XAndISSN: 13691643AndVolume Number: 2011AndStart Page: 457532AndDate: 2011 Revise Search
- 1From: Sarcoma. (Vol. 2019) Peer-ReviewedOne way to enhance quality of life for patients with metastatic sarcoma is to maximize time off chemotherapy--a chemotherapy-free interval. While image-guided ablation of sarcoma metastases may reduce the need for...
- 2From: Sarcoma. (Vol. 2021) Peer-ReviewedBackground. Standard therapy for localized soft tissue sarcoma (STS) is wide, limb-sparing resection. For intermediate- or high-grade tumors, (neo)adjuvant therapies are frequently added to the treatment plan. In this...
- 3From: Sarcoma. (Vol. 2020) Peer-ReviewedBackground. Follow-up of high-grade bone sarcoma patients with repeated radiological imaging aims at early detection of recurrent disease or distant metastasis. Repeated radiological imaging does expose (mostly young)...
- 4From: Sarcoma. (Vol. 2020) Peer-ReviewedThe purpose of this study is to evaluate the benefit of reviewing scout CT images, obtained for routine oncologic surveillance, for the early identification of pathologic bony lesions. A retrospective review was...
- 5From: Sarcoma. (Vol. 2021) Peer-ReviewedIntroduction. Adult rhabdomyosarcoma is a rare tumour that has an inferior survival compared to the paediatric patient population. The reason for this consistently worse outcome remains mostly unknown. It has been...
- 6From: Sarcoma. (Vol. 2020) Peer-ReviewedLimb salvage surgery is now the preferred procedure for bone tumor surgery. To decrease the risk of local recurrence, it is crucial to obtain adequate resection margins. The obtained margins must be evaluated...
- 7From: Sarcoma. (Vol. 2022) Peer-ReviewedBackground. Soft-tissue sarcomas (STSs) are rare tumors; they represent 1% of all tumors in adults. There are new diagnostic techniques to differentiate tumor types, and surgery continues to be the most important...
- 8From: Sarcoma. Peer-ReviewedRhabdomyosarcoma (RMS) and rhabdoid tumors (RT) are rare soft-tissue malignancies with the highest incidence in infants, children, and adolescents. Advanced, recurrent, and/or metastatic RMS and RT exhibit poor response...
- 9From: Sarcoma. (Vol. 2020) Peer-ReviewedBackground. This study explored how patients with metastatic gastrointestinal stromal tumour (GIST) experience the psychosocial challenges associated with their disease and its treatment, as well as how that experience...
- 10From: Sarcoma. (Vol. 2021) Peer-ReviewedSynopsis. For ALTs, the utility of chest surveillance has not been well defined. This study suggests that chest imaging does not have a significant role in the surveillance of ALTs. Advanced local imaging and more...
- 11From: Sarcoma. (Vol. 2021) Peer-ReviewedBackground. The majority of patients with localized Ewing sarcoma will remain disease-free long term, but for those who suffer recurrence, successful treatment remains a challenge. Identification of clinicopathologic...
- 12From: Sarcoma. (Vol. 2022) Peer-ReviewedRhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma for which subsets of patients have longstanding unmet clinical needs. For example, children with alveolar rhabdomyosarcoma and metastases at...
- 13From: Sarcoma. (Vol. 2020) Peer-ReviewedSoft tissue sarcomas (STS) constitute a heterogeneous group of rare solid tumors associated with significant morbidity and mortality. The evaluation and treatment of STS require a multidisciplinary team with extensive...
- 14From: Sarcoma. (Vol. 2019) Peer-ReviewedDoes reimplantation of sterilized tumor bone for reconstruction provide outcome benefits in intercalary osteosarcoma based on the potential immunogenic effect of reimplanted sterilized tumor tissue? Of 720 cases of...
- 15From: Sarcoma. (Vol. 2020) Peer-ReviewedBackground. Clear cell chondrosarcoma (CCC) represents less than 6% of all chondrosarcomas, and thus, our understanding of this rare entity is limited. Analyzing clinical characteristics and treatment patterns, thus...
- 16From: Sarcoma. (Vol. 2021) Peer-ReviewedIntroduction. Osteosarcoma is the most common sarcoma of bone. Pelvic osteosarcoma presents a significant therapeutic challenge due to potential late symptom onset, metastatic dissemination at diagnosis, and inherent...
- 17From: Sarcoma. Peer-ReviewedPatients with localized relapse of soft-tissue sarcoma (STS) after anthracycline-based chemotherapy have a dismal prognosis, particularly when surgery is not possible. To facilitate resection and improve long-term tumor...
- 18From: Sarcoma. Peer-ReviewedBackground. Malignant peripheral nerve sheath tumors (MPNSTs) are rare and aggressive soft tissue sarcomas (STS) that, because of their origin, are operated by several surgical subspecialties. This may cause differences...
- 19From: Sarcoma. (Vol. 2023) Peer-ReviewedBackground. Time to treatment initiation (TTI) is a quality metric in cancer care. The purpose of this study is to determine the accuracy of TTI data from a single cancer center registry that reports to the National...
- 20From: Sarcoma. (Vol. 2021) Peer-ReviewedIntroduction. Paratesticular sarcomas are defined as tumors that arise within the scrotum and include the subsites of epididymis, spermatic cord, and tunica vaginalis and represent the most common type of GU sarcoma. The...