A Pilot Study of Liposomal Doxorubicin Combined with Bevacizumab followed by Bevacizumab Monotherapy in Patients with Advanced Kaposi Sarcoma.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 07 2019
Historique:
received: 29 10 2018
revised: 11 01 2019
accepted: 08 04 2019
pubmed: 14 4 2019
medline: 23 9 2020
entrez: 14 4 2019
Statut: ppublish

Résumé

VEGF-A is important in the pathogenesis of Kaposi sarcoma, and bevacizumab has a response rate of 31%. We explored the combination of bevacizumab with liposomal doxorubicin in patients with Kaposi sarcoma. Patients with Kaposi sarcoma requiring systemic therapy were enrolled in one of two cohorts. Cohort 1 included patients with human immunodeficiency virus (HIV)-negative Kaposi sarcoma or with HIV-associated Kaposi sarcoma who would not be expected to respond to antiretroviral therapy (ART) alone (i.e., either stable or progressive Kaposi sarcoma on ART). Cohort 2 included all other patients with HIV-associated Kaposi sarcoma. Patients were treated with six cycles of liposomal doxorubicin with bevacizumab every 3 weeks followed by up to 11 cycles of bevacizumab alone. Sixteen patients were enrolled: 10 (two HIV negative) in cohort 1 and six in cohort 2. Fourteen patients had advanced disease (AIDS Clinical Trials Group T Pegylated liposomal doxorubicin in combination with bevacizumab has activity in advanced Kaposi sarcoma, but it is unclear whether the combination yields better outcomes than liposomal doxorubicin used alone.

Identifiants

pubmed: 30979736
pii: 1078-0432.CCR-18-3528
doi: 10.1158/1078-0432.CCR-18-3528
pmc: PMC6635024
mid: NIHMS1527088
doi:

Substances chimiques

Vascular Endothelial Growth Factor A 0
liposomal doxorubicin 0
Bevacizumab 2S9ZZM9Q9V
Polyethylene Glycols 3WJQ0SDW1A
Doxorubicin 80168379AG

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4238-4247

Subventions

Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States
Organisme : Intramural NIH HHS
ID : Z99 CA999999
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIC SC006537-23
Pays : United States

Informations de copyright

©2019 American Association for Cancer Research.

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Auteurs

Ramya Ramaswami (R)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland. ramya.ramaswami@nih.gov.

Thomas S Uldrick (TS)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Mark N Polizzotto (MN)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Kathleen M Wyvill (KM)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Priscila Goncalves (P)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Anaida Widell (A)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Kathryn Lurain (K)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Seth M Steinberg (SM)

Biostatistics and Data Management Section, Center for Cancer Research, NCI, Bethesda, Maryland.

William Douglas Figg (WD)

Molecular Pharmacology Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

Giovanna Tosato (G)

Laboratory of Cellular Oncology, Center for Cancer Research, NCI, Bethesda, Maryland.

Denise Whitby (D)

Viral Oncology Section, AIDS and Cancer Virus Program, Leidos-Biomedical, Frederick National Laboratory for Cancer Research, Frederick, Maryland.

Robert Yarchoan (R)

HIV & AIDS Malignancy Branch, Center for Cancer Research, NCI, Bethesda, Maryland.

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Classifications MeSH