Literature DB >> 12916459

Combined-modality treatment of localized soft tissue sarcomas of the extremities.

Courtney L Scaife1, Peter W Pisters.   

Abstract

Over the past 20 years, considerable progress has been made in the treatment of patients with extremity soft tissue sarcomas. There has been a migration away from amputation toward treatment by excision plus radiation for most patients with localized tumors. Decisions about the optimal use and sequencing of surgery and radiation remain complex. Whereas it is clear that local control is probably not impacted significantly by the treatment sequence, rates of wound complication, fibrosis, and edema are affected by the treatment sequence. In addition, recent single-institution reports indicate that some carefully selected patients can be treated by surgery alone. The recent data evaluating treatment by surgery alone and treatment sequencing variables do not lead to a situation in which clear, uniform recommendations for treatment can be made for many patients with extremity soft tissue sarcomas. Indeed, treatment planning for patients with extremity soft tissue sarcoma in the new millennium is infinitely more complex than it was in the era when amputation was the primary treatment for these patients. Considerable clinical experience and multidisciplinary input are required for optimal treatment planning for these patients. Future research should be directed at refining the indications for specific therapies, reducing the toxicities of local therapies, and developing more effective systemic therapies.

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Year:  2003        PMID: 12916459     DOI: 10.1016/s1055-3207(03)00003-6

Source DB:  PubMed          Journal:  Surg Oncol Clin N Am        ISSN: 1055-3207            Impact factor:   3.495


  9 in total

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Journal:  Curr Treat Options Oncol       Date:  2015-03

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Journal:  Ther Adv Med Oncol       Date:  2020-07-03       Impact factor: 8.168

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Journal:  ISRN Surg       Date:  2011-04-11

5.  Prognostic factors in adult soft tissue sarcoma treated with surgery combined with radiotherapy: a retrospective single-center study on 164 patients.

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Review 6.  Malignant Peripheral Nerve Sheath Tumors State of the Science: Leveraging Clinical and Biological Insights into Effective Therapies.

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Review 7.  Malignant peripheral nerve sheath tumor: models, biology, and translation.

Authors:  Bandarigoda N Somatilaka; Ali Sadek; Renee M McKay; Lu Q Le
Journal:  Oncogene       Date:  2022-04-07       Impact factor: 8.756

8.  Targeting Refractory Sarcomas and Malignant Peripheral Nerve Sheath Tumors in a Phase I/II Study of Sirolimus in Combination with Ganetespib (SARC023).

Authors:  AeRang Kim; Yao Lu; Scott H Okuno; Denise Reinke; Ophélia Maertens; John Perentesis; Mitali Basu; Pamela L Wolters; Thomas De Raedt; Sant Chawla; Rashmi Chugh; Brian A Van Tine; Geraldine O'Sullivan; Alice Chen; Karen Cichowski; Brigitte C Widemann
Journal:  Sarcoma       Date:  2020-01-30

9.  Establishment and characterization of patient-derived cancer models of malignant peripheral nerve sheath tumors.

Authors:  Rieko Oyama; Fusako Kito; Mami Takahashi; Emi Hattori; Rei Noguchi; Yoko Takai; Marimu Sakumoto; Zhiwei Qiao; Shunichi Toki; Masato Sugawara; Yoshikazu Tanzawa; Eisuke Kobayashi; Fumihiko Nakatani; Shintaro Iwata; Akihiko Yoshida; Akira Kawai; Tadashi Kondo
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  9 in total

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