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      Soft‐tissue sarcoma in adults: An update on the current state of histiotype‐specific management in an era of personalized medicine

      1 , 2 , 3
      CA: A Cancer Journal for Clinicians
      Wiley

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          Most cited references216

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          Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft-tissue sarcoma: a randomised controlled phase 3 trial.

          Effective targeted treatment is unavailable for most sarcomas and doxorubicin and ifosfamide-which have been used to treat soft-tissue sarcoma for more than 30 years-still have an important role. Whether doxorubicin alone or the combination of doxorubicin and ifosfamide should be used routinely is still controversial. We assessed whether dose intensification of doxorubicin with ifosfamide improves survival of patients with advanced soft-tissue sarcoma compared with doxorubicin alone.
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            A pilot trial using lymphocytes genetically engineered with an NY-ESO-1-reactive T-cell receptor: long-term follow-up and correlates with response.

            Although adoptive cell therapy can be highly effective for the treatment of patients with melanoma, the application of this approach to the treatment of other solid tumors has been limited. The observation that the cancer germline (CG) antigen NY-ESO-1 is expressed in 70% to 80% and in approximately 25% of patients with synovial cell sarcoma and melanoma, respectively, prompted us to perform this first-in-man clinical trial using the adoptive transfer of autologous peripheral blood mononuclear cells that were retrovirally transduced with an NY-ESO-1-reactive T-cell receptor (TCR) to heavily pretreated patients bearing these metastatic cancers.
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              Soft-tissue sarcomas of adults; study of pathological prognostic variables and definition of a histopathological grading system.

              The pathological features of 155 adult patients with soft-tissue sarcomas were studied retrospectively, in an attempt to set up a grading system for these tumors. As the first step, seven histological criteria (tumor differentiation, cellularity, importance of nuclear atypia, presence of malignant giant cells, mitosis count, pattern of tumor necrosis and presence of vascular emboli) were evaluated in a monofactorial analysis. Five of these (tumor differentiation, cellularity, mitosis count, tumor necrosis, and vascular emboli) were correlated with the advent of metastases and with survival. A multivariate analysis, using a Cox model, selected a minimal set of three factors (tumor differentiation, mitosis count, and tumor necrosis) the combination of which was necessary and sufficient to retain all the prognostic information. A grading system was elaborated, which turned out to be correlated with the advent of metastasis and with patients' survival. A second multivariate analysis introducing clinical prognostic features showed that the histological grade was the most important prognostic factor for soft-tissue sarcomas. Thus, this grading system appears to be highly interesting because of its prognostic value and the facility of its elaboration. However, its reproducibility should be tested.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                CA: A Cancer Journal for Clinicians
                CA A Cancer J Clin
                Wiley
                0007-9235
                1542-4863
                May 2020
                April 10 2020
                May 2020
                : 70
                : 3
                : 200-229
                Affiliations
                [1 ]Division of Surgical Oncology Department of Surgery Emory University Atlanta Georgia
                [2 ]Department of Surgery Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy
                [3 ]Division of Surgical Oncology Winship Cancer Institute Emory University Hospital Midtown Atlanta Georgia
                Article
                10.3322/caac.21605
                32275330
                27565a0b-7f06-4b51-99a3-493dd6054818
                © 2020

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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