Systemic treatment of soft-tissue sarcoma—gold standard and novel therapies
M Linch, AB Miah, K Thway, IR Judson… - Nature reviews Clinical …, 2014 - nature.com
Soft-tissue sarcoma (STS) is a rare and heterogeneous group of tumours that comprise
approximately 1% of all adult cancers, and encompass over 50 different subtypes. These …
approximately 1% of all adult cancers, and encompass over 50 different subtypes. These …
Combination of Genomic Landsscape and 3D Culture Functional Assays Bridges Sarcoma Phenotype to Target and Immunotherapy
F de Nigris, C Meo, W Palinski - Cells, 2023 - mdpi.com
Genomic-based precision medicine has not only improved tumour therapy but has also
shown its weaknesses. Genomic profiling and mutation analysis have identified alterations …
shown its weaknesses. Genomic profiling and mutation analysis have identified alterations …
[HTML][HTML] The landscape of drug sensitivity and resistance in sarcoma
Sarcomas are rare malignancies with over 100 distinct histological subtypes. Their rarity and
heterogeneity pose significant challenges to identifying effective therapies, and approved …
heterogeneity pose significant challenges to identifying effective therapies, and approved …
Hyperglycemia associated with targeted oncologic treatment: mechanisms and management
JW Goldman, MA Mendenhall, SR Rettinger - The oncologist, 2016 - academic.oup.com
Molecularly targeted cancer therapy has rapidly changed the landscape of oncologic care,
often improving patients' prognosis without causing as substantial a quality-of-life decrement …
often improving patients' prognosis without causing as substantial a quality-of-life decrement …
Molecular targeted therapy for advanced or metastatic soft tissue sarcoma
J Yuan, X Li, S Yu - Cancer Control, 2021 - journals.sagepub.com
Soft tissue sarcomas are a form of rare and heterogeneous neoplasms with high recurrence
rate and mortality. Over the past decades, less progress has been achieved. Surgical …
rate and mortality. Over the past decades, less progress has been achieved. Surgical …
[HTML][HTML] Phase-II trials in osteosarcoma recurrences: a systematic review of past experience
N Omer, MC Le Deley, S Piperno-Neumann… - European Journal of …, 2017 - Elsevier
Background The most appropriate design of Phase-II trials evaluating new therapies in
osteosarcoma remains poorly defined. Objective To study consistency in phase-II clinical …
osteosarcoma remains poorly defined. Objective To study consistency in phase-II clinical …
[HTML][HTML] Targeting angiosarcomas of the soft tissues: A challenging effort in a heterogeneous and rare disease
ME Weidema, YMH Versleijen-Jonkers… - Critical Reviews in …, 2019 - Elsevier
Angiosarcomas are rare malignant tumors with a heterogeneous clinical presentation and
generally poor prognosis. It has been difficult to establish consistent molecular …
generally poor prognosis. It has been difficult to establish consistent molecular …
Advances in sarcoma gene mutations and therapeutic targets
Sarcomas are rare and complex malignancies that have been associated with a poor
prognostic outcome. Over the last few decades, traditional treatment with surgery and/or …
prognostic outcome. Over the last few decades, traditional treatment with surgery and/or …
Emerging therapies for adult soft tissue sarcoma
S Radaelli, S Stacchiotti, PG Casali… - Expert review of …, 2014 - Taylor & Francis
Soft tissue sarcoma (STS) are a broad group of rare tumors. Cornerstone of treatment is
surgery. Complementary radiotherapy is recommended in high-risk STS arising from …
surgery. Complementary radiotherapy is recommended in high-risk STS arising from …
Combination treatment with sorafenib and everolimus regresses a doxorubicin-resistant osteosarcoma in a PDOX mouse model
Background/Aim: Osteosarcoma is a rare but recalcitrant type of bone cancer. To discover
an effective therapy for osteosarcoma, we used a patient-derived orthotopic xenograft …
an effective therapy for osteosarcoma, we used a patient-derived orthotopic xenograft …