Evidence map›Paper›PMID 28848723›Full record

ArticleJournal of hepatocellular carcinoma2017

A Phase I trial using local regional treatment, nonlethal irradiation, intratumoral and systemic polyinosinic-polycytidylic acid polylysine carboxymethylcellulose to treat liver cancer: in search of the abscopal effect.

Andrew N de la Torre, Sohail Contractor, Ismael Castaneda, Charles S Cathcart, Dolly Razdan, David Klyde, Piotr Kisza, Sharon F Gonzales, Andres M Salazar

Open access · goldAbstract read
In one paragraph

Article in Journal of hepatocellular carcinoma, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Pathogen Molecular Pattern Receptor Agonists: Treating Cancer by Mimicking Infection.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Review
  13. Article
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  15. Cancer immunotherapy beyond immune checkpoint inhibitors.Journal of hematology & oncology · 2018
    Review
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 1 country.

Andrew N de la TorreDepartment of Surgery, St Joseph's Regional Medical Center, Paterson.
Sohail ContractorDepartment of Interventional Radiology, Rutgers New Jersey Medical School-University Hospital.
Ismael CastanedaDepartment of Surgery, St Joseph's Regional Medical Center, Paterson.
Charles S CathcartDepartment of Radiation Oncology, Beth Israel Medical Center, Newark.
Dolly RazdanDepartment of Radiation Oncology, Clara Maas Hospital, Belleville, NJ.
David KlydeDepartment of Interventional Radiology, Rutgers New Jersey Medical School-University Hospital.
Piotr KiszaDepartment of Interventional Radiology, Rutgers New Jersey Medical School-University Hospital.
Sharon F GonzalesDepartment of Interventional Radiology, Rutgers New Jersey Medical School-University Hospital.
Andres M SalazarOncovir, Washington, DC, USA.
Rutgers New Jersey Medical SchoolSt. Joseph’s University Medical Center · USUniversity Hospital, Newark · USOncovir (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo determine the safety of an approach to immunologically enhance local treatment of hepatocellular cancer (HCC) by combining nonlethal radiation, local regional therapy with intratumoral injection, and systemic administration of a potent Toll-like receptor (TLR) immune adjuvant.

methodsPatients with HCC not eligible for liver transplant or surgery were subject to: 1) 3 fractions of 2-Gy focal nonlethal radiation to increase tumor antigen expression, 2) intra-/peri-tumoral (IT) injection of the TLR3 agonist, polyinosinic-polycytidylic acid polylysine carboxymethylcellulose (poly-ICLC), to induce an immunologic "danger" response in the tumor microenvironment with local regional therapy, and 3) systemic boosting of immunity with intramuscular poly-ICLC. Primary end points were safety and tolerability; secondary end points were progression-free survival (PFS) and overall survival (OS) at 6 months, 1 year, and 2 years.

resultsEighteen patients with HCC not eligible for surgery or liver transplant were treated. Aside from 1 embolization-related severe adverse event, all events were ≤grade II. PFS was 66% at 6 months, 39% at 12 months, and 28% at 24 months. Overall 1-year survival was 69%, and 2-year survival 38%. In patients <60 years old, 2-year survival was 62.5% vs. 11.1% in patients aged >60 years (

conclusionIntra-tumoral injection of the TLR3 agonist poly-ICLC in patients with HCC is safe and tolerable when combined with local nonlethal radiation and local regional treatment. Further work is in progress to evaluate if this approach improves survival compared to local regional treatment alone and characterize changes in anticancer immunity.

Indexed as

autologous vaccinehuman trialimmunotherapyliver cancerToll-like receptor

Identifiers

PMID28848723
PMCPMC5557908
OpenAlexW2742647944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.