Evidence map›Paper›PMID 33912442›Full record

ArticleFrontiers in oncology2021

High TIL, HLA, and Immune Checkpoint Expression in Conventional High-Grade and Dedifferentiated Chondrosarcoma and Poor Clinical Course of the Disease.

Sjoerd P F T Nota, Ahmad Al-Sukaini, Shalin S Patel, Francesco Sabbatino, G Petur Nielsen, Vikram Deshpande, Jennifer H Yearley, Soldano Ferrone, Xinhui Wang, Joseph H Schwab

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Sjoerd P F T NotaDepartment of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Ahmad Al-SukainiDepartment of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Shalin S PatelDepartment of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Francesco SabbatinoSection of Orthopaedic Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
G Petur NielsenSection of Orthopaedic Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Vikram DeshpandeSection of Orthopaedic Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Jennifer H YearleyDepartment of Translational Medicine, Merck & Co., Inc., Kenilworth, NJ, United States.
Soldano FerroneDepartment of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Xinhui WangSection of Orthopaedic Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Joseph H SchwabDepartment of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Harvard University · USMassachusetts General Hospital · USMerck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

T cell plasticity, fusion proteins and CAR T cell-based immunotherapy of head and neck cancerR01DE028172 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI WANG, XINHUI · 2018 to 2022
$1.9M
Potential role of brachyury in HLA class I antigen processing machinery component downregulation in chordoma cellsR03CA253319 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FERRONE, SOLDANO, SCHWAB, JOSEPH HASBROUCK · 2020 to 2020
$167k
B7-H3 CAR T cell-based immunotherapy combined with Losartan to counteract desmoplasia for the treatment of Pancreatic Ductal Adenocarcinoma (PDAC)R03CA249542 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FERRONE, CRISTINA R., FERRONE, SOLDANO · 2021 to 2021
$167k
NCI NIH HHS R03 CA249542NCI NIH HHS R03 CA253319NIDCR NIH HHS R01 DE028172
6 · The paper itself

Abstract

purposeThe aim of this study was to characterize chondrosarcoma tumor infiltration by immune cells and the expression of immunologically relevant molecules. This information may contribute to our understanding of the role of immunological events in the pathogenesis of chondrosarcoma and to the rational design of immunotherapeutic strategies. PATIENTS AND

methodsA tissue microarray (TMA) containing 52 conventional and 24 dedifferentiated chondrosarcoma specimens was analyzed by immunohistochemical staining for the expression of parameters associated with tumor antigen-specific immune responses, namely, CD4

resultsCD8

conclusionThe tumor infiltration by lymphocytes suggests that chondrosarcoma is immunogenic. Defects in HLA class I antigen and expression of the checkpoint molecules B7-H3 and PD-1/PD-L1 suggest that tumor cells utilize escape mechanisms to avoid immune recognition and destruction. This data implies that chondrosarcoma will benefit from strategies that enhance the immunogenicity of tumor antigens and/or counteract the escape mechanisms.

Indexed as

B7-H3chondrosarcomaHLA class IPD-L1T cell infiltration

Identifiers

PMID33912442
PMCPMC8071983
OpenAlexW3155950857

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Registered trials

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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.