Evidence map›Paper›PMID 25384911›Full record

ArticleCancer immunology, immunotherapy : CII2015

Development of photodynamic therapy regimens that control primary tumor growth and inhibit secondary disease.

Madeeha Shams, Barbara Owczarczak, Patricia Manderscheid-Kern, David A Bellnier, Sandra O Gollnick

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

63 citing papers in PubMed, 110 citations in OpenAlex.

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  18. Cytotoxic Effects of Combinative ZnPcSInternational journal of molecular sciences · 2023
    Article
  19. Article
  20. Light-enhanced VEGFFrontiers in immunology · 2023
    Article

3 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

5 authors at 1 institution in 1 country.

Madeeha ShamsDepartment of Cell Stress Biology, PDT Center, Roswell Park Cancer Institute, Elm & Carlton Sts, Buffalo, NY, 14263, USA.
Barbara Owczarczak
Patricia Manderscheid-Kern
David A Bellnier
Sandra O Gollnick
Roswell Park Comprehensive Cancer Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Photodynamic Therapy (PDT) Mechanisms: Tumor ImmunityR01CA098156 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI GOLLNICK, SANDRA O. · 2003 to 2013
$3.6M
Peroxiredoxin 1 in radiotherapy of lung cancerR01CA109480 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI PARK, YOUNG-MEE · 2004 to 2007
$995k
NCI NIH HHS CA109480NCI NIH HHS CA16056NCI NIH HHS CA98156NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA098156NCI NIH HHS R01 CA109480
6 · The paper itself

Abstract

Effective therapy for advanced cancer often requires treatment of both primary tumors and systemic disease that may not be apparent at initial diagnosis. Numerous studies have shown that stimulation of the host immune system can result in the generation of anti-tumor immune responses capable of controlling metastatic tumor growth. Thus, there is interest in the development of combination therapies that both control primary tumor growth and stimulate anti-tumor immunity for control of metastatic disease and subsequent tumor growth. Photodynamic therapy (PDT) is an FDA-approved anticancer modality that has been shown to enhance anti-tumor immunity. Augmentation of anti-tumor immunity by PDT is regimen dependent, and PDT regimens that enhance anti-tumor immunity have been defined. Unfortunately, these regimens have limited ability to control primary tumor growth. Therefore, a two-step combination therapy was devised in which a tumor-controlling PDT regimen was combined with an immune-enhancing PDT regimen. To determine whether the two-step combination therapy enhanced anti-tumor immunity, resistance to subsequent tumor challenge and T cell activation and function was measured. The ability to control distant disease was also determined. The results showed that the novel combination therapy stimulated anti-tumor immunity while retaining the ability to inhibit primary tumor growth of both murine colon (Colon26-HA) and mammary (4T1) carcinomas. The combination therapy resulted in enhanced tumor-specific T cell activation and controlled metastatic tumor growth. These results suggest that PDT may be an effective adjuvant for therapies that fail to stimulate the host anti-tumor immune response.

Indexed as

AnimalsAntineoplastic AgentsChlorophyllColonic NeoplasmsDihematoporphyrin EtherFemaleLymphocyte ActivationMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CNeoplasm MetastasisPhotochemotherapyPhotosensitizing AgentsRandom AllocationT-LymphocytesTransfection2-(1-hexyloxyethyl)-2-devinyl pyropheophorbide-aAntineoplastic AgentsChlorophyllDihematoporphyrin EtherPhotosensitizing Agents

Identifiers

PMID25384911
PMCPMC4341021
OpenAlexW2066659514

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.