2015
DOI: 10.1200/jco.2015.60.8505
|View full text |Cite
|
Sign up to set email alerts
|

Paclitaxel Given Once Per Week With or Without Bevacizumab in Patients With Advanced Angiosarcoma: A Randomized Phase II Trial

Abstract: The primary objective was met in both treatment arms. However, the present data do not support additional clinical investigation of combined paclitaxel/bevacizumab for the treatment of advanced AS.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
115
4
3

Year Published

2016
2016
2022
2022

Publication Types

Select...
7
1

Relationship

2
6

Authors

Journals

citations
Cited by 157 publications
(125 citation statements)
references
References 20 publications
3
115
4
3
Order By: Relevance
“…Addition of bevacizumab to taxane-based chemotherapy was studied in randomized phase II trial of Ray-Coquard et al [23]. Patients were treated with paclitaxel weekly (90 mg/m 2 ) or combination of paclitaxel (90 mg/m 2 ) weekly and bevacizumab (10 mg/kg biweekly).…”
Section: Discussionmentioning
confidence: 99%
“…Addition of bevacizumab to taxane-based chemotherapy was studied in randomized phase II trial of Ray-Coquard et al [23]. Patients were treated with paclitaxel weekly (90 mg/m 2 ) or combination of paclitaxel (90 mg/m 2 ) weekly and bevacizumab (10 mg/kg biweekly).…”
Section: Discussionmentioning
confidence: 99%
“…Two phase II studies of chemotherapy in advanced angiosarcoma have been carried out by the French Sarcoma Group [27,31]. The ANGIOTAX study was a single arm phase II study of weekly paclitaxel as first-line treatment in 30 patients with angiosarcoma [31].…”
Section: Angiosarcomamentioning
confidence: 99%
“…The schedule was active and well tolerated, but eventual outcomes were still poor with a median TTP of 4 months and median OS of 8 months. A subsequent randomized phase II study investigated the addition of bevacizumab to paclitaxel in the first-line (2/3 of patients) and nonfirst-line setting in 52 patients [27]. The addition of bevacizumab increased toxicity substantially but did not improve outcomes, although interestingly the outcomes of the entire patient cohort were better than in the previous study, or case series, with median PFS of 6.6 months and median OS of 19.5 months on the paclitaxel arm versus 15.9 months for the paclitaxel and bevacizumab arm.…”
Section: Angiosarcomamentioning
confidence: 99%
See 1 more Smart Citation
“…The combination of bevacizumab with doxorubicin in a phase II study in unselected STS subtypes failed to surpass efficacy levels expected for doxorubicin alone, with a safety signal that suggested an increase in cardiac toxicity [46]. Optimism for bevacizumab in STS of blood vessel origin was quelled by a randomised phase II trial that failed to demonstrate incremental efficacy from the addition of bevacizumab to standard paclitaxel chemotherapy [47]. …”
Section: Recent Phase III Studies That Failed To Improve On Standard mentioning
confidence: 99%