Evidence map›Paper›PMID 23942212›Full record

ArticleBiomaterials2013

Anti-CD30 antibody conjugated liposomal doxorubicin with significantly improved therapeutic efficacy against anaplastic large cell lymphoma.

Ommoleila Molavi, Xiao-Bing Xiong, Donna Douglas, Norm Kneteman, Satoshi Nagata, Ira Pastan, Quincy Chu, Afsaneh Lavasanifar, Raymond Lai

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  9. Nanoparticles for Effective Combination Therapy of Cancer.International journal of nanotechnology and nanomedicine · 2016
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Ommoleila MolaviDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Xiao-Bing XiongFaculty of Pharmacy and Pharmaceutical Science, University of Alberta, Edmonton, Alberta, Canada.
Donna DouglasDepartment of Surgery, University of Alberta, Edmonton, Alberta, Canada.
Norm KnetemanDepartment of Surgery, University of Alberta, Edmonton, Alberta, Canada.
Satoshi NagataCancer Biology Research Center, Sanford Research/USD, SD, USA.
Ira PastanLaboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Quincy ChuDepartment of Oncology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Afsaneh Lavasanifar *Faculty of Pharmacy and Pharmaceutical Science, University of Alberta, Edmonton, Alberta, Canada.
Raymond Lai *Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
University of Alberta · CANational Cancer Institute · USSanford Research · USTabriz University of Medical Sciences · IR

Funding

Immunotoxin Therapy of Solid and Hematopoietic Tumors: Preclinical StudiesZIABC008753 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PASTAN, IRA · 2009 to 2024
$33.1M
IMMUNOTOXIN THERAPY OF SOLID AND HEMATOPOIETIC TUMORS: PRECLINICAL STUDIESZ01BC008753 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PASTAN, IRA · 1996 to 2008
$3.2M
CENTER FOR CANCER BIOLOGY RESEARCHP20RR024219 · NCRR · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2011 to 2011
$2.3M
CIHRIntramural NIH HHS Z01 BC008753NCRR NIH HHS 1P20RR024219-01A2NCRR NIH HHS P20 RR024219
6 · The paper itself

Abstract

The use of nano-carriers has been shown to improve the delivery and efficacy of chemotherapeutic agents in cancer patients. Recent studies suggest that decoration of the surface of nano-carriers with various targeting moieties may further improve the overall therapeutic efficacy. In this study, we compared the therapeutic efficacy of Doxil(®) (commercial doxorubicin-loaded liposomes) and that of Doxil(®) conjugated with anti-CD30 antibodies (CD30-targeted Doxil(®)) in treating anaplastic large cell lymphoma (ALCL), a type of T-cell lymphoma characterized by a high CD30 expression. Compared to Doxil(®), the CD30-targeted Doxil(®) showed a significantly higher binding affinity to ALCL cells (5.3% versus 27%, p = 0.005) and a lower inhibitory concentration at 50% (IC50) in-vitro (32.6 μg/mL versus 12.6 μg/mL, p = 0.006). In a SCID mouse xenograft model, CD30-targeted Doxil(®) inhibited tumor growth more significantly than the unconjugated formulation; specifically, tumors in mice treated with CD30-targeted Doxil(®) were significantly smaller than those in mice treated with Doxil(®) (average, 117 mm(3) versus 270 mm(3), p = 0.001) at 18 days after the tumors were inoculated. Our findings have provided the proof-of-principle of using CD30-targeted nano-carriers to treat cancers that are characterized by a high level of CD30 expression, such as ALCL.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsCell Line, TumorDisease Models, AnimalDoxorubicinKi-1 AntigenLymphoma, Large-Cell, AnaplasticMaleMiceMice, SCIDNanoparticlesPolyethylene GlycolsAntibodies, MonoclonalAntineoplastic AgentsDoxorubicinKi-1 Antigenliposomal doxorubicinPolyethylene GlycolsAnaplastic large cell lymphomaCD30DoxorubicinLiposomeTargeted therapy

Identifiers

PMID23942212
PMCPMC3796131
OpenAlexW2145879538

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.