Evidence map›Paper›PMID 35710741›Full record

Trial reportNature communications2022

Pilot study of bempegaldesleukin in combination with nivolumab in patients with metastatic sarcoma.

Sandra P D'Angelo, Allison L Richards, Anthony P Conley, Hyung Jun Woo, Mark A Dickson, Mrinal Gounder, Ciara Kelly, Mary Louise Keohan, Sujana Movva, Katherine Thornton and 20 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03282344 (A Pilot Study of NKTR-214 and Nivolumab in Selected Patients With Locally Advanced/Metastatic Sarcoma), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.9field-weighted citation impact, top 2% 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.

NCT03282344 phase2active not recruitingnot on this map

A Pilot Study of NKTR-214 and Nivolumab in Selected Patients With Locally Advanced/Metastatic Sarcoma (CA209-9EM)

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2017 to 2027Enrolled88ConditionsSARCOMAArmsNKTR-214, Nivolumab
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 54 citations in OpenAlex.

  1. Cemiplimab in Locally Advanced or Metastatic Secondary Angiosarcomas (CEMangio): A Phase II Clinical Trial and Biomarker Analyses.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  2. Trial
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  4. Review
  5. Article
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  7. Article
  8. Association of Circulating T Cell and Tumor Microenvironment Profiles with Immune Checkpoint Blockade Outcomes in Sarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Angiosarcoma: Role of Immunotherapy.Current treatment options in oncology · 2025
    Review
  20. Article
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

30 authors at 2 institutions in 1 country.

Sandra P D'Angelo *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA. dangelos@mskcc.org.ORCID http://orcid.org/0000-0002-3736-3783
Allison L Richards *Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Anthony P ConleyDepartment of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Hyung Jun WooMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Mark A DicksonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Mrinal GounderDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Ciara KellyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.ORCID http://orcid.org/0000-0002-4393-8088
Mary Louise KeohanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Sujana MovvaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Katherine ThorntonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Evan RosenbaumDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Ping ChiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Benjamin NacevDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.ORCID http://orcid.org/0000-0003-4991-2492
Jason E ChanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.ORCID http://orcid.org/0000-0003-0552-8544
Emily K SlotkinDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Hannah KieslerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Travis AdamsonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.ORCID http://orcid.org/0000-0001-5055-0842
Lilan LingMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Pavitra RaoMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Shreyaskumar PatelDepartment of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jonathan A LivingstonDepartment of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-1337-3282
Samuel SingerDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Narasimhan P AgaramDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Cristina R AntonescuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.ORCID http://orcid.org/0000-0002-9717-8205
Andrew KoffProgram in Molecular Biology, Memorial Sloan Kettering Cancer, New York City, NY, USA.
Joseph P ErinjeriDepartment of Interventional Radiology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Sinchun HwangDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Li-Xuan QinDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Mark T A DonoghueMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
William D TapDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Memorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Targeting Oncogenic Pathways in Genetically Complex SarcomasP50CA217694 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI William D. Tap · 2018 to 2026
$21.5M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA217694
6 · The paper itself

Abstract

PD-1 blockade (nivolumab) efficacy remains modest for metastatic sarcoma. In this paper, we present an open-label, non-randomized, non-comparative pilot study of bempegaldesleukin, a CD122-preferential interleukin-2 pathway agonist, with nivolumab in refractory sarcoma at Memorial Sloan Kettering/MD Anderson Cancer Centers (NCT03282344). We report on the primary outcome of objective response rate (ORR) and secondary endpoints of toxicity, clinical benefit, progression-free survival, overall survival, and durations of response/treatment. In 84 patients in 9 histotype cohorts, all patients experienced ≥1 adverse event and treatment-related adverse event; 1 death was possibly treatment-related. ORR was highest in angiosarcoma (3/8) and undifferentiated pleomorphic sarcoma (2/10), meeting predefined endpoints. Results of our exploratory investigation of predictive biomarkers show: CD8 + T cell infiltrates and PD-1 expression correlate with improved ORR; upregulation of immune-related pathways correlate with improved efficacy; Hedgehog pathway expression correlate with resistance. Exploration of this combination in selected sarcomas, and of Hedgehog signaling as a predictive biomarker, warrants further study in larger cohorts.

Indexed as

Antineoplastic Agents, ImmunologicalNeoplasms, Second PrimarySarcomaHedgehog ProteinsHumansInterleukin-2NivolumabPilot ProjectsProgrammed Cell Death 1 ReceptorAntineoplastic Agents, ImmunologicalHedgehog ProteinsInterleukin-2NivolumabProgrammed Cell Death 1 Receptor

Identifiers

PMID35710741
PMCPMC9203519
OpenAlexW4283029304

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.