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Journal ArticleDOI

Management of osteosarcoma.

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TLDR
This study heralds a new era of clinical investigation into osteosarcoma, with the promise of valuable biologic insights and rapid evaluation of investigational strategies.
Abstract
Improving cure rates for osteosarcoma continues to be a major challenge. The clinical management of individual patients is exacting and requires a skilled, experienced team including a surgeon, pathologist, oncologist, and radiologist, with support from specialist nurses and rehabilitation teams. Outcomes from treatment have improved little in 20 years and remain disappointing. Chemotherapy for osteosarcoma is among the most grueling of any given for solid tumors, and treatment of the primary tumor is associated with permanent disability of some degree in a significant proportion of patients. New systemic treatments remain beyond the horizon. In recognition of these difficulties, an international cooperation has begun with the opening of a randomized trial, European and American Osteosarcoma (EURAMOS) 1, in Europe and the United States. This study heralds a new era of clinical investigation into osteosarcoma, with the promise of valuable biologic insights and rapid evaluation of investigational strategies. Osteosarcoma should always be treated under the guidance of a specialist team, and we recommend that whenever possible, patients be offered entry into EURAMOS 1 or other well-designed clinical trials.

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Citations
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Journal ArticleDOI

Osteosarcoma treatment - where do we stand? A state of the art review.

TL;DR: The current state of the art of systemic osteosarcoma therapy is reviewed by focusing on the experiences of cooperative osteosARcoma groups, shedding light on questions and challenges posed by the aggressiveness of the tumor, and potential future directions that may be critical to progress in the prognosis of high-grade osteosArcoma.
Journal ArticleDOI

Incidence and survival of malignant bone sarcomas in England 1979-2007

TL;DR: This population‐based study has allowed us to confidently define the English incidence and survival rates of both the commoner bone tumours such as osteosarcoma, and rarer entities such as chordoma as well as groups with inferior outcome.
Journal ArticleDOI

Sequelae of osteosarcoma medical therapy: a review of rare acute toxicities and late effects

TL;DR: Reducing the complications of osteosarcoma therapy is an important goal that will require the identification of clear prognostic indicators, the development of biologically-based therapies, and improved antidotes for the active anti-osteosARcoma cytotoxic drugs.
Journal ArticleDOI

Challenges in the recruitment of adolescents and young adults to cancer clinical trials.

TL;DR: The adolescent and young adult (AYA) oncology population has seen inferior progress in cancer survival compared with younger children and older adults over the past 25 years, and survival rates are particularly poor for AYA‐specific diseases such as sarcomas.
Journal ArticleDOI

Programmed cell death ligand 1 expression in osteosarcoma.

TL;DR: It is shown, for the first time, that high levels of PDL1 are expressed in a subset of osteosarcoma, and PDL2 expression is positively correlated with TILs, suggesting this subset of patients may benefit from anti-PD-L1 immunotherapy.
References
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Journal ArticleDOI

Preoperative Chemotherapy for Osteogenic Sarcoma: Selection of Postoperative Adjuvant Chemotherapy Based on the Response of the Primary Tumor to Preoperative Chemotherapy

TL;DR: The value of thorough histologic examination in predicting survival in responding patients and in helping identify patients whose disease‐free survival rate can be substantially increased if they are given alternative postoperative adjuvant chemotherapy after failing to have a good response to preoperative chemotherapy are demonstrated.
Journal ArticleDOI

Integration of interferon-alpha/beta signalling to p53 responses in tumour suppression and antiviral defence.

TL;DR: It is shown that transcription of the p53 gene is induced by IFN-α/β, accompanied by an increase in p53 protein level, and that p53 is critical for antiviral defence of the host.
Journal ArticleDOI

Chemotherapy for nonmetastatic osteogenic sarcoma: the Memorial Sloan-Kettering experience.

TL;DR: Intensive chemotherapy can achieve DFS for a high proportion of patients with osteogenic sarcoma and histologic response to preoperative chemotherapy cannot be assessed at diagnosis, although it is a powerful predictor of DFS.
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