Impact of Biomarker-Matched Therapies on Outcomes in Patients with Sarcoma Enrolled in Early-Phase Clinical Trials (SAMBA 101).


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
01 05 2023
Historique:
received: 22 11 2022
revised: 30 12 2022
accepted: 24 02 2023
medline: 2 5 2023
pubmed: 15 4 2023
entrez: 14 4 2023
Statut: ppublish

Résumé

Developing new therapeutics for any of the more than 100 sarcoma subtypes presents a challenge. After progression from standard therapies, patients with sarcoma may be referred for enrollment in early-phase trials. This study aimed to investigate whether enrollment in biomarker-matched early-phase clinical trials leads to better outcomes for patients with advanced sarcoma. In this retrospective analysis, investigational treatment characteristics and longitudinal survival outcomes were analyzed in patients with biopsy-confirmed sarcoma enrolled in early-phase trials at MD Anderson Cancer Center from May 2006 to July 2021. Five hundred eighty-seven patients were included [405 soft tissue, 122 bone, 60 gastrointestinal stromal tumor (GIST); median of three prior lines of therapy]. Most common subtypes were leiomyosarcoma (17.2%), liposarcoma (14.0%), and GIST (10.2%). Molecular testing was available for 511 patients (87.1%); 221 patients (37.6%) were treated in matched trials. Overall response rate was 13.1% matched compared with 4.9% in unmatched (P < 0.001); the clinical benefit rate at 6 months was 43.9% vs. 19.9% (P < 0.001). Progression-free survival was longer for patients in matched trials (median, 5.5 vs. 2.4 months; P < 0.001), and overall survival was also superior for patients in matched trials (median, 21.5 vs. 12.3 months; P < 0.001). The benefit of enrollment in matched trials was maintained when patients with GIST were excluded from the analysis. Enrollment in biomarker-matched early-phase trials is associated with improved outcomes in heavily pretreated patients with metastatic sarcoma. Molecular testing of tumors from patients with advanced sarcoma and enrollment in matched trials is a reasonable therapeutic strategy.

Identifiants

pubmed: 37058010
pii: 725715
doi: 10.1158/1078-0432.CCR-22-3629
pmc: PMC10150251
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1708-1718

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA242845
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000371
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA180964
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA273168
Pays : United States

Informations de copyright

©2023 The Authors; Published by the American Association for Cancer Research.

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Auteurs

Roberto Carmagnani Pestana (R)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hospital Israelita Albert Einstein, São Paulo, Brazil.

Justin T Moyers (JT)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Medicine, Division of Hematology and Oncology, The University of California, Irvine, Orange, California.

Jason Roszik (J)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Shiraj Sen (S)

Sarah Cannon Research Institute, Nashville, Tennessee.

David S Hong (DS)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Aung Naing (A)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Cynthia E Herzog (CE)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Siqing Fu (S)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Sarina A Piha-Paul (SA)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Jordi Rodon (J)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Timothy A Yap (TA)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Daniel D Karp (DD)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Apostolia M Tsimberidou (AM)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Shubham Pant (S)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Maria A Zarzour (MA)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ravin Ratan (R)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Vinod Ravi (V)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Robert S Benjamin (RS)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Alexander J Lazar (AJ)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Wei-Lien Wang (WL)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Najat Daw (N)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Jonathan B Gill (JB)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Douglas J Harrison (DJ)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Valerae O Lewis (VO)

Department of Orthopedic Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Christina L Roland (CL)

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Shreyaskumar R Patel (SR)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

J Andrew Livingston (JA)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Neeta Somaiah (N)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Joseph A Ludwig (JA)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Anthony P Conley (AP)

Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Nelson Hamerschlak (N)

Hospital Israelita Albert Einstein, São Paulo, Brazil.

Richard Gorlick (R)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Funda Meric-Bernstam (F)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

Vivek Subbiah (V)

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

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