A systematic meta‐analysis of randomized controlled trials of adjuvant chemotherapy for localized resectable soft‐tissue sarcoma

N Pervaiz, N Colterjohn, F Farrokhyar… - … Journal of the …, 2008 - Wiley Online Library
BACKGROUND. The use of adjuvant chemotherapy to treat adults with localized resectable
soft‐tissue sarcoma remains controversial. The objective of this systematic review was to …

Uterine leiomyosarcoma: A review of the literature and update on management options

ME Roberts, JT Aynardi, CS Chu - Gynecologic Oncology, 2018 - Elsevier
Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely
aggressive malignancy associated with a poor overall prognosis. Women affected may vary …

[HTML][HTML] Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up☆

A Gronchi, AB Miah, AP Dei Tos, N Abecassis… - Annals of …, 2021 - Elsevier
Highlights•This Clinical Practice Guideline provides key recommendations on the
management of soft tissue and visceral sarcomas.•Recommendations have been agreed …

Soft tissue and visceral sarcomas: ESMO–EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up

PG Casali, N Abecassis, S Bauer, R Biagini… - Annals of …, 2018 - annalsofoncology.org
Soft tissue sarcomas (STSs) gather over 80 histological entities, with even more molecular
subsets, characterised by a low to very low incidence in all populations. The majority of …

Soft tissue and visceral sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

ESMO/European Sarcoma Network … - Annals of oncology …, 2014 - pubmed.ncbi.nlm.nih.gov
Soft tissue and visceral sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment
and follow-up Soft tissue and visceral sarcomas: ESMO Clinical Practice Guidelines for diagnosis …

Soft tissue sarcoma, version 2.2016, NCCN clinical practice guidelines in oncology

M Von Mehren, RL Randall, RS Benjamin… - Journal of the National …, 2016 - jnccn.org
Soft tissue sarcomas (STS) are rare solid tumors of mesenchymal cell origin that display a
heterogenous mix of clinical and pathologic characteristics. STS can develop from fat …

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

I Judson, J Verweij, H Gelderblom, JT Hartmann… - The lancet …, 2014 - thelancet.com
Background 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 …

[HTML][HTML] An open-label, multicenter, phase II study of bevacizumab for the treatment of angiosarcoma and epithelioid hemangioendotheliomas

M Agulnik, JL Yarber, SH Okuno, M Von Mehren… - Annals of …, 2013 - Elsevier
Background To determine efficacy and safety of bevacizumab, a recombinant humanized
antibody against vascular endothelial growth factor (VEGF), in the treatment of metastatic or …

Soft tissue sarcoma, version 2.2022, NCCN clinical practice guidelines in oncology

M von Mehren, JM Kane, M Agulnik, MM Bui… - Journal of the National …, 2022 - jnccn.org
Soft tissue sarcomas (STS) are rare malignancies of mesenchymal cell origin that display a
heterogenous mix of clinical and pathologic characteristics. STS can develop from fat …

2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline

TJ Smith, J Khatcheressian, GH Lyman… - Journal of Clinical …, 2006 - ascopubs.org
Purpose To update the 2000 American Society of Clinical Oncology guideline on the use of
hematopoietic colony-stimulating factors (CSF). Update Methodology The Update …