NLMSF Knowledge Hub

General LMS Research Highlights

Curated publications, research updates, clinical trials, and educational links relevant to the broader sarcoma community.

NLMSF Research Grants

2026–2027 Research Grant Announcement

LOI deadline: April 15, 2025

The National Leiomyosarcoma Foundation (NLMSF) invites letters of intent (LOIs) for pilot studies to launch new research trajectories in LMS, with a focus on basic and translational science. Clinical interventional trials are out of scope.

  • Total award: $50,000 per year for 2 years (indirects ≤ 10%).
  • Scope includes biomarkers, imaging, computational biology, radiomics, and lab‑based translational studies.
  • Human sample studies require IRB approval (or waiver) prior to award.

Submission contacts: matthew.hemming@umassmemorial.org and alessandra.maleddu@cuanschutz.edu

Research Updates

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NATIONAL LEIOMYOSARCOMA FOUNDATION

2026-2027 RESEARCH GRANT ANNOUNCEMENT

NLMSF Empowering patients through information / education / support

LOI deadline: April 15th, 2025

Please submit to Matthew Hemming, M.D., PhD.: matthew.hemming@umassmemorial.org and Alessandra Maleddu M.D.: alessandra.maleddu@cuanschutz.edu

Introduction: The National Leiomyosarcoma Foundation (NLMSF) is dedicated to meeting the needs of leiomyosarcoma (LMS) patients, caregivers and families through education and research. In order to facilitate advances in the treatment of LMS through research, the NLMSF is accepting research proposals for pilot studies that will launch “out of the box” ideas and new research trajectories to move the field forward.

Scope of the award/ areas of interest: All direct funds must be used to support LMS research. Proposals involving any scientific discipline are allowed including those related to biomarkers and imaging. This award was created to support basic and translational research. Other highly translational projects that are not based in a traditional wet lab may be considered (for example: in silico computational biology, radiomics, etc.); however, investigators who are considering submitting a non-traditional research project are highly encouraged to discuss the appropriateness of their project ahead of time. Clinical research (interventional trials) will not be supported by this award; however, work studying human samples and annotated data sets obtained from clinical trials is allowed. Studies requiring human samples must show documentation of IRB approval prior to awarding of funds (or document waivers if applicable).

Letter of Intent (LOI) Overview: The NLMSF seeks LOIs for research grant funding. The total award will be $50,000 per year for 2 years. Indirect costs should not exceed 10% of the total budget.
The LOI should consist of:
1) Proposed research (2 page maximum)
2) Applicant NIH Biosketch

Key Dates:
LOI due: April 15th, 2025
Invitations for full proposal sent: May 30th, 2025
Full proposal due: August 31st, 2025
Announcement: November 2025
Funding start date: January 2026

_____________________________________________________________________________________________________________________

2025

Clinical outcomes following stereotactic radiosurgery for brain metastases from sarcoma primaries: An international multicenter analysis (Cancer. 2025 Jul 1;131(13):e35931. doi: 10.1002/cncr.35931.)

Leiomyosarcoma Therapeutic Approaches and Future Directions (7 April 2025) available on‑line in the Hematology/Oncology Clinics of North America (22 May 2025)
https://www.sciencedirect.com/science/article/abs/pii/S0889858825000450?via%3Dihub

Emerging Role of Blood‑based Biomarkers in Sarcomas (2 April 2025) available on‑line in the Hematology/Oncology Clinics of North America (22 May 2025)
https://www.sciencedirect.com/science/article/abs/pii/S0889858825000401?via%3Dihub

Myxoid Leiomyosarcoma of the Uterus – A Case Report (2 Apr 2025) in Oncology Letters

 
Comprehensive mutational profiling identifies new driver events in cutaneous leiomyosarcoma https://academic.oup.com/bjd/article-abstract/192/2/335/7818451

Plain language summary

Cutaneous leiomyosarcoma (or ‘cLMS’ for short) is a type of skin tumour... These findings give us a better understanding of the biology of cLMS.

Exploration of the mutational landscape of cutaneous leiomyoma confirms FH as a driver gene    https://doi.org/10.1093/bjd/ljae432

 

2024

Dr. Patricia Pautier — research update in the New England Journal of Medicine

Published November 27, 2024
N Engl J Med 2024;391:2057-2058
DOI: 10.1056/NEJMc2412479

VOL. 391 NO. 21

Doxorubicin–Trabectedin in Leiomyosarcoma | New England Journal of Medicine

CLINICAL TRIALS:

Randomized controlled, open‑label, phase IIb/III study of lurbinectedin in combination with doxorubicin versus doxorubicin alone as first‑line treatment in patients with metastatic leiomyosarcoma. NCT06088290

Randomized controlled, open‑label, phase IIb/III study of lurbinectedin + doxorubicin vs doxorubicin alone | JCO

Study of ADI‑PEG 20 or Placebo Plus Gem and Doc in Previously Treated Subjects With Leiomyosarcoma (ARGSARC)

July 25, 2024 updated by: Polaris Group

ADI‑PEG 20 or Placebo Plus Gemcitabine and Docetaxel in Previously Treated Subjects With Leiomyosarcoma (ARGSARC): A Randomized, Double Blind, Multi‑Center Phase 3 Trial

To compare the efficacy and safety in subjects with advanced or metastatic LMS previously treated with an anthracycline.

Study Overview

This is a global, multicenter, randomized, double‑blind, placebo‑controlled, parallel‑group phase 3 trial...

www.mskcc.org/cancer-care/clinical-trials/24-147

Frontiers | Leiomyosarcoma of the abdomen and retroperitoneum; a systematic review (frontiersin.org) <https://www.frontiersin.org/journals/surgery/articles/10.3389/fsurg.2024.1375483/full>
 

doi: 10.1200/JCO.24.00358
Phase Ib Study for the Combination of Doxorubicin, Dacarbazine, and Nivolumab as the Upfront Treatment in Patients With Advanced Leiomyosarcoma: A Study by the Spanish Sarcoma Group (GEIS)

Principle investigator: Dr. Javier Martin–Broto, esteemed member of the NLMSF International LMS Research Roundtable
https://pubmed.ncbi.nlm.nih.gov/39356980

Purpose: Doxorubicin can induce immunogenic cell death (ICD). Combining doxorubicin and dacarbazine with nivolumab may enhance therapeutic efficacy via ICD synergy. Conclusion: The scheme is feasible and well tolerated; clinical activity is encouraging; HMGB1 supports ICD relevance. Further research is underway in LMS.

Immunotherapy in Sarcoma: Current Data and Promising Strategies
Authors: Georgina E. Wood, Christian Meyer, Florent Petitprez, Sandra P. D’Angelo — Authors Info & Affiliations
ASCO Educational Book (May 2024)

TRANSLATIONAL CANCER MECHANISMS AND THERAPY | MAY 15 2024
Developing Novel Genomic Risk Stratification Models in Soft Tissue and Uterine Leiomyosarcoma

Josephine K. Dermawan — Clin Cancer Res (2024) 30 (10): 2260–2271.

https://doi.org/10.1158/1078-0432.CCR-24-0148

 
Leiomyosarcoma – Continuing Education Activity (28 Feb 2024)
 

2023

New therapeutics for soft tissue sarcomas — Overview of current immunotherapy and future directions of STS (14 May 2023)
Frontiers in Oncology article — Gyuhee Seong and Sandra D’Angelo
 

High Grade Sarcomas with Myogenic Differentiation Harboring Hotspot PDGFRB Mutations (May 2023)
https://www.sciencedirect.com/science/article/abs/pii/S089339522300008X
NOTE: LMS discussed in this article

The Biology and Treatment of LMS (Apr 2023)

Targeting the Molecular and Immunologic Features of Leiomyosarcoma (31 Mar 2023)
https://www.mdpi.com/2072-6694/15/7/2099

Sequential Targeting of Retinoblastoma and DNA Synthesis Pathways Is a Therapeutic Strategy for Sarcomas (15 Mar 2023) — MD Anderson
https://pubmed.ncbi.nlm.nih.gov/36603130/

Not All Leiomyosarcomas Are the Same: How to Best Classify LMS (8 Mar 2023) https://link.springer.com/article/10.1007/s11864-023-01067-2

Therapeutic advances in leiomyosarcoma (8 Mar 2023) — Frontiers in Oncology
https://www.frontiersin.org/articles/10.3389/fonc.2023.1149106/full

Clinical characteristics of sarcoma cases with long-term disease control on trabectedin (1 Mar 2023)
https://pubmed.ncbi.nlm.nih.gov/36857355/

 

2022

Molecular subtypes of leiomyosarcoma: Moving toward a consensus (2 Nov 2022)
https://onlinelibrary.wiley.com/doi/full/10.1002/ctd2.149

Landmark Series: A Review of Landmark Studies in the Treatment of Primary Localized Retroperitoneal Sarcoma (2 Nov 2022) https://link.springer.com/article/10.1245/s10434-022-12517-w

CLINICAL TRIALS: TARGETED THERAPY (2 Aug 2022)
Phase II Clinical Trial of Eribulin–Gemcitabine Combination Therapy in Previously Treated Patients With Advanced Liposarcoma or Leiomyosarcoma
https://aacrjournals.org/clincancerres/article-abstract/28/15/3225/707113/...

Phase II Clinical Trial of Eribulin–Gemcitabine... (2 Aug 2022)

A phase Ib/II study of lenvatinib + eribulin (LEADER): Efficacy updates (2 Aug 2023)

Retroperitoneal LMS Nomogram Model (3 Jul 2022)

Sounding the Alarm on Leiomyosarcoma Recurrence: Role of ctDNA (13 Jun 2022)

PRESS RELEASE NEWS — UNESBULIN for LMS (3 Jun 2022)

Surgical management strategy for LMS of IVC (3 Jun 2022)

Preclinical Modeling of LMS Identifies Susceptibility to Transcriptional CDK Inhibitors — Dr. Matt Hemming (1 Jun 2022)

Preoperative Differentiation of Uterine Leiomyomas and Leiomyosarcomas (13 Apr 2022)
Full publication

What Clinical Trials Are Needed for Treatment of Leiomyosarcoma? (11 Mar 2022)

Proteomic and Metabolomic Profiling in STS (16 Feb 2022)

 

2021

Surgical resection of LMS of the IVC: case series + review

Relationships between highly recurrent tumor suppressor alterations in 489 LMS

Large scale multiomic analysis suggests mechanisms of resistance to IO in LMS

Multiomic analysis to reveal distinct profiles of uterine and non‑uterine LMS

 

2020

 

2019

Genomic Evolutionary Patterns of Leiomyosarcoma and Liposarcoma
PubMed  |  Clinical Cancer Research

 

2018

Soft Tissue and Uterine Leiomyosarcoma (10 Jan 2018)