Evidence map›Paper›PMID 34976834›Full record

ArticleFrontiers in oncology2021

Case Report: Exceptional Response to Nivolumab Plus Ipilimumab in a Young Woman With TFE3-SFPQ Fusion Translocation-Associated Renal Cell Carcinoma.

Dylan J Martini, Caroline S Jansen, Lara R Harik, Sean T Evans, T Anders Olsen, Viraj A Master, Haydn T Kissick, Mehmet Asim Bilen

Abstract readCase Reports
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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Dylan J MartiniDepartment of Medicine, Massachusetts General Hospital, Boston, MA, United States.
Caroline S JansenDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, United States.
Lara R HarikDepartment of Pathology, Emory University School of Medicine, Atlanta, GA, United States.
Sean T EvansDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, United States.
T Anders OlsenDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, United States.
Viraj A MasterDepartment of Urology, Emory University School of Medicine, Atlanta, GA, United States.
Haydn T KissickDepartment of Urology, Emory University School of Medicine, Atlanta, GA, United States.
Mehmet Asim BilenDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, United States.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
Examining the Mechanisms of Immune Cell Infiltration and Organization in a Murine Model of Renal Cancer and in Primary Human Renal TumorsF30CA243250 · NCI · EMORY UNIVERSITY · PI JANSEN, CAROLINE STEWART · 2020 to 2023
$214k
NCI NIH HHS F30 CA243250NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

Translocation-associated renal cell carcinoma (tRCC) is a rare, aggressive malignancy that primarily affects children and young adults. There is no clear consensus on the most effective treatment for tRCC and there are no biomarkers of response to treatments in these patients. We present a case of a 23 year-old female with metastatic tRCC to the lungs who was started on treatment with nivolumab and ipilimumab. She had a complete radiographic response to treatment and has been progression-free for over 18 months. Immunofluorescence imaging performed on the baseline primary tumor sample showed significant intratumoral immune infiltration. Importantly, these cells are present in niches characterized by TCF1+ CD8+ T cells. Histopathologic investigation showed the presence of lymphocytes in the fibrovascular septae and foci of lymphovascular invasion. Furthermore, lymphovascular invasion and intratumor niches with TCF1+ CD8+ T cells may predict a favorable response to treatment with nivolumab and ipilimumab. These findings have significant clinical relevance given that immune checkpoint inhibitors are approved for several malignancies and predictive biomarkers for response to treatment are lacking. Importantly, the identification of these TCF1+ CD8+ T cells may guide treatment for patients with tRCC, which is a rare malignancy without a consensus first-line treatment option.

Indexed as

combination immune checkpoint therapyexceptional responderintratumoral immune nicherare malignancyTCF1+ CD8+ T cellstranslocation-associated RCC

Identifiers

PMID34976834
PMCPMC8716393

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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.