Evidence map›Paper›PMID 34965948›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Long-term Follow-up and Patterns of Response, Progression, and Hyperprogression in Patients after PD-1 Blockade in Advanced Sarcoma.

Nicholas D Klemen, Sinchun Hwang, Martina Bradic, Evan Rosenbaum, Mark A Dickson, Mrinal M Gounder, Ciara M Kelly, Mary L Keohan, Sujana Movva, Katherine A Thornton and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Stereotactic body radiation therapy for sarcoma pulmonary metastases.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2023
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Treatment of De-Differentiated Liposarcoma in the Era of Immunotherapy.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Review
  14. First communication on the efficacy of combinedJournal for immunotherapy of cancer · 2022
    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

19 authors at 1 institution in 1 country.

Nicholas D KlemenDepartment of Surgery, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Sinchun HwangDepartment of Radiology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0002-6402-3020
Martina BradicMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0001-6078-5311
Evan RosenbaumDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0002-7499-1279
Mark A DicksonDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Mrinal M GounderDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Ciara M KellyDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0002-4393-8088
Mary L KeohanDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Sujana MovvaDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Katherine A ThorntonDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Ping ChiDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Benjamin A NacevDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0003-4991-2492
Jason E ChanDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0003-0552-8544
Edmund K BartlettDepartment of Surgery, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0002-0923-153X
Allison L RichardsMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Samuel SingerDepartment of Surgery, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Mark T A DonoghueMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
William D TapDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.ORCID 0000-0001-7779-2796
Sandra P D'AngeloDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, Manhattan, New York.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Targeting Oncogenic Pathways in Genetically Complex SarcomasP50CA217694 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Marc Ladanyi · 2018 to 2026
$21.5M
SPORE in Soft Tissue SarcomaP50CA140146 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SPRIGGS, DAVID R · 2010 to 2014
$11.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA140146NCI NIH HHS P50 CA217694
6 · The paper itself

Abstract

purposeProgrammed cell death protein 1 (PD-1) blockade can mediate objective responses in advanced sarcomas, but their durability has not been established and it is unclear if hyperprogressive disease (HPD) occurs in sarcomas treated with PD-1 inhibitors. EXPERIMENTAL

designWe pooled patients who were treated prospectively with nivolumab or pembrolizumab as monotherapy or with bempegaldesleukin, epacadostat, ipilimumab, or talimogene laherparepvec. We did a new independent assessment for HPD and analyzed clinical, pathologic, and genomic data from baseline tumor biopsies. Our primary endpoint was the incidence of HPD; secondary endpoints were clinical or genomic correlates of response or HPD.

resultsWe treated 134 patients with advanced sarcoma from 2015 to 2019. Twenty-one patients (16%) had a complete or partial response (CR/PR), and 30% of responses were durable for over 2 years. Forty-eight (36%) patients had stable disease (SD), 45 (34%) had progressive disease without HPD (PD), and 15 (11%) had HPD. Five patients (4%) were not evaluable for HPD. The sarcoma subtypes, sites of metastasis, clinical course, and genomic alterations in patients with PD and HPD were similar, except HPD tumors were smaller at baseline.

conclusionsIn patients with advanced sarcoma, PD-1 blockade can mediate durable responses. HPD occurs in sarcoma at an incidence that is similar to what has been reported in other solid tumors, but patients with HPD were clinically and biologically similar to those who had PD. Further research is required to establish whether HPD is a biologically distinct phenomenon and whether a theoretical risk of HPD should influence patient management.

Indexed as

MelanomaOncolytic VirotherapySarcomaDisease ProgressionFollow-Up StudiesHumansProgrammed Cell Death 1 ReceptorProgrammed Cell Death 1 Receptor

Identifiers

PMID34965948
PMCPMC8898277
OpenAlexW4200477034

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.