Evidence map›Paper›PMID 24572574›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Selective treatment and monitoring of disseminated cancer micrometastases in vivo using dual-function, activatable immunoconjugates.

Bryan Q Spring, Adnan O Abu-Yousif, Akilan Palanisami, Imran Rizvi, Xiang Zheng, Zhiming Mai, Sriram Anbil, R Bryan Sears, Lawrence B Mensah, Ruth Goldschmidt and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

92 citing papers in PubMed, 129 citations in OpenAlex.

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32 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 1 country.

Bryan Q SpringWellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114.
Adnan O Abu-Yousif
Akilan Palanisami
Imran Rizvi
Xiang Zheng
Zhiming Mai
Sriram Anbil
R Bryan Sears
Lawrence B Mensah
Ruth Goldschmidt
S Sibel Erdem
Esther Oliva
Tayyaba Hasan
Harvard University · USMassachusetts General Hospital · US

Funding

Small Molecule Enhancers of Photodynamic Therapy for Skin CancerP01CA084203 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Tayyaba Hasan · 2001 to 2026
$27.9M
Ovarian Cancer PDT: Multi-intracellular targeting and Image-guided dosimetryR01CA160998 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2011 to 2015
$2.0M
EXPERIMENTAL PHOTOIMMUNOTHERAPY OF OVARIAN CANCERR01AR040352 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 1992 to 2006
$1.6M
Targeted Photoactivatable Nanocells to Image and Treat Metastic Ovarian CancerRC1CA146337 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2009 to 2010
$971k
Hyperspectral Microendscopy to Monitor VEGF During Pancreatic Cancer TherapyF32CA144210 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SPRING, BRYAN QUILTY · 2010 to 2012
$153k
NCI NIH HHS F32 CA144210NCI NIH HHS F32-CA144210NCI NIH HHS P01 CA084203NCI NIH HHS P01-CA084203NCI NIH HHS R01 CA160998NCI NIH HHS R01-CA160998NCI NIH HHS RC1 CA146337NCI NIH HHS RC1-CA146337NIAMS NIH HHS R01 AR040352NIAMS NIH HHS R01-AR40352
6 · The paper itself

Abstract

Drug-resistant micrometastases that escape standard therapies often go undetected until the emergence of lethal recurrent disease. Here, we show that it is possible to treat microscopic tumors selectively using an activatable immunoconjugate. The immunoconjugate is composed of self-quenching, near-infrared chromophores loaded onto a cancer cell-targeting antibody. Chromophore phototoxicity and fluorescence are activated by lysosomal proteolysis, and light, after cancer cell internalization, enabling tumor-confined photocytotoxicity and resolution of individual micrometastases. This unique approach not only introduces a therapeutic strategy to help destroy residual drug-resistant cells but also provides a sensitive imaging method to monitor micrometastatic disease in common sites of recurrence. Using fluorescence microendoscopy to monitor immunoconjugate activation and micrometastatic disease, we demonstrate these concepts of "tumor-targeted, activatable photoimmunotherapy" in a mouse model of peritoneal carcinomatosis. By introducing targeted activation to enhance tumor selectively in complex anatomical sites, this study offers prospects for catching early recurrent micrometastases and for treating occult disease.

Indexed as

AnimalsAntibodies, MonoclonalDrug Delivery SystemsEndoscopyFemaleFluorescenceImmunoconjugatesImmunotherapyLightMiceMonitoring, ImmunologicNeoplasm MicrometastasisOvarian NeoplasmsPhototherapySensitivity and SpecificityAntibodies, MonoclonalImmunoconjugatesactivatable imaging agentactivatable therapeutic agentmolecular imagingovarian cancerphotodynamic therapy

Identifiers

PMID24572574
PMCPMC3956156
OpenAlexW1998966049

What OpenQuestion holds

Textmetadata
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.