Evidence map›Paper›PMID 38236580›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2024

Phase II Study of Eribulin plus Pembrolizumab in Metastatic Soft-tissue Sarcomas: Clinical Outcomes and Biological Correlates.

Candace L Haddox, Michael J Nathenson, Emanuele Mazzola, Jia-Ren Lin, Joanna Baginska, Allison Nau, Jason L Weirather, Edwin Choy, Adrian Marino-Enriquez, Jeffrey A Morgan and 6 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
11.7field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  8. Article
  9. Treatments and outcomes of primary and metastatic spinal angiosarcoma patients: study of 29 consecutive cases.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
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  16. Leiomyosarcoma Therapeutic Approaches and Future Directions.Hematology/oncology clinics of North America · 2025
    Review
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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

16 authors at 4 institutions in 1 country.

Candace L Haddox *Sarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-4223-0632
Michael J Nathenson *Sarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-8888-4482
Emanuele MazzolaDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-0561-7336
Jia-Ren LinDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-4702-7705
Joanna BaginskaCenter for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-5182-7575
Allison NauDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-2001-2431
Jason L WeiratherDepartment of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-0556-0616
Edwin ChoyDivision of Hematology Oncology, Massachusetts General Cancer Center, Boston, Massachusetts.ORCID 0000-0001-9896-8084
Adrian Marino-EnriquezDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-7680-9901
Jeffrey A MorganSarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0009-0006-6476-161X
Gregory M CoteDivision of Hematology Oncology, Massachusetts General Cancer Center, Boston, Massachusetts.ORCID 0000-0003-0181-886X
Priscilla MerriamSarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-8675-998X
Andrew J WagnerSarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-4384-9448
Peter K SorgerDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-3364-1838
Sandro SantagataDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-7528-9668
Suzanne GeorgeSarcoma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-1284-8493
Dana-Farber Cancer Institute · USHarvard University · USBrigham and Women's Hospital · USCenter for Cancer Research · US

Funding

Pre-cancer atlases of cutaneous and hematologic origin (PATCH Center)U2CCA233262 · NCI · HARVARD MEDICAL SCHOOL · PI SANTAGATA, SANDRO · 2018 to 2023
$8.7M
Advancing technologies for the collection and analysis of high dimensional immunoprofiles and tumor imagesR50CA274277 · NCI · HARVARD MEDICAL SCHOOL · PI Jia-Ren Lin · 2022 to 2026
$879k
NCI NIH HHS R50 CA274277NCI NIH HHS U2C CA233262
6 · The paper itself

Abstract

purposeEribulin modulates the tumor-immune microenvironment via cGAS-STING signaling in preclinical models. This non-randomized phase II trial evaluated the combination of eribulin and pembrolizumab in patients with soft-tissue sarcomas (STS). PATIENTS AND

methodsPatients enrolled in one of three cohorts: leiomyosarcoma (LMS), liposarcomas (LPS), or other STS that may benefit from PD-1 inhibitors, including undifferentiated pleomorphic sarcoma (UPS). Eribulin was administered at 1.4 mg/m2 i.v. (days 1 and 8) with fixed-dose pembrolizumab 200 mg i.v. (day 1) of each 21-day cycle, until progression, unacceptable toxicity, or completion of 2 years of treatment. The primary endpoint was the 12-week progression-free survival rate (PFS-12) in each cohort. Secondary endpoints included the objective response rate, median PFS, safety profile, and overall survival (OS). Pretreatment and on-treatment blood specimens were evaluated in patients who achieved durable disease control (DDC) or progression within 12 weeks [early progression (EP)]. Multiplexed immunofluorescence was performed on archival LPS samples from patients with DDC or EP.

resultsFifty-seven patients enrolled (LMS, n = 19; LPS, n = 20; UPS/Other, n = 18). The PFS-12 was 36.8% (90% confidence interval: 22.5-60.4) for LMS, 69.6% (54.5-89.0) for LPS, and 52.6% (36.8-75.3) for UPS/Other cohorts. All 3 patients in the UPS/Other cohort with angiosarcoma achieved RECIST responses. Toxicity was manageable. Higher IFNα and IL4 serum levels were associated with clinical benefit. Immune aggregates expressing PD-1 and PD-L1 were observed in a patient that completed 2 years of treatment.

conclusionsThe combination of eribulin and pembrolizumab demonstrated promising activity in LPS and angiosarcoma.

Indexed as

Antibodies, Monoclonal, HumanizedFuransHemangiosarcomaKetonesLeiomyosarcomaLiposarcomaPolyether PolyketidesSarcomaHumansLipopolysaccharidesTreatment OutcomeTumor MicroenvironmentAntibodies, Monoclonal, HumanizederibulinFuransKetonesLipopolysaccharidespembrolizumabPolyether Polyketides

Identifiers

PMID38236580
PMCPMC10982640
OpenAlexW4390972528

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.