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 …

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 …

[HTML][HTML] The landscape of drug sensitivity and resistance in sarcoma

A Al Shihabi, PJ Tebon, HTL Nguyen… - Cell stem cell, 2024 - cell.com
Sarcomas are rare malignancies with over 100 distinct histological subtypes. Their rarity and
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 …

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 …

[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 …

[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 …

Advances in sarcoma gene mutations and therapeutic targets

P Gao, NA Seebacher, F Hornicek, Z Guo… - Cancer treatment …, 2018 - Elsevier
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 …

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 …

Combination treatment with sorafenib and everolimus regresses a doxorubicin-resistant osteosarcoma in a PDOX mouse model

T Higuchi, N Sugisawa, K Miyake, H Oshiro… - Anticancer …, 2019 - ar.iiarjournals.org
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 …