Dramatic Reduction of Distant Pancreatic Metastases Using Local Light Activation of Verteporfin with Nab-Paclitaxel.

abscopal effect metastatic disease pancreatic cancer photodynamic therapy

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
18 Nov 2021
Historique:
received: 12 10 2021
revised: 06 11 2021
accepted: 15 11 2021
entrez: 27 11 2021
pubmed: 28 11 2021
medline: 28 11 2021
Statut: epublish

Résumé

Despite substantial drug development efforts, pancreatic adenocarcinoma (PDAC) remains a difficult disease to treat, and surgical resection is the only potentially curative option. Unfortunately, 80% of patients are ineligible for surgery due to the presence of invasive disease and/or distant metastases at the time of diagnosis. Treatment strategies geared towards reclassifying these patients as surgical candidates by reducing metastatic burden represents the most promising approach to improve long-term survival. We describe a photodynamic therapy (PDT) based approach that, in combination with the first-line chemotherapeutic nab-paclitaxel, effectively addresses distant metastases in three separate orthotopic PDAC models in immunodeficient mice. In addition to effectively controlling local tumor growth, PDT plus nab-paclitaxel primes the tumor to elicit systemic effects and reduce or abrogate metastases. This combination dramatically inhibits (up to 100%) the eventual development of metastases in models of early stage PDAC, and completely eliminates metastasis in 55% of animals with already established distant disease in late-stage models. Our findings suggest that this light activation process initiates local biological and/or physiological changes within the tumor microenvironment that can be leveraged to treat both localized and distant disease, and potentially reclassify patients with previously inoperable disease as surgical candidates.

Identifiants

pubmed: 34830934
pii: cancers13225781
doi: 10.3390/cancers13225781
pmc: PMC8616053
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIH HHS
ID : P01CA084203
Pays : United States
Organisme : NIH HHS
ID : R01CA156177
Pays : United States
Organisme : NIH HHS
ID : R21CA220143
Pays : United States
Organisme : NIH HHS
ID : S100D012326
Pays : United States

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Auteurs

Michael Pigula (M)

Department of Chemistry, Scripps Research, La Jolla, CA 92037, USA.

Zhiming Mai (Z)

Wellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

Sriram Anbil (S)

David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

Myung-Gyu Choi (MG)

Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul 137-040, Korea.

Kenneth Wang (K)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN 55902, USA.

Edward Maytin (E)

Department of Dermatology, Cleveland Clinic, Cleveland, OH 44195, USA.

Brian Pogue (B)

Department of Engineering Sciences, Dartmouth College, Hanover, NH 03755, USA.

Tayyaba Hasan (T)

Wellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

Classifications MeSH