Rationale and design of the PAMSARC (pasireotide as maintenance treatment with monthly deep intramuscular injection in SSTR2/3/5-expressing synovial sarcoma and desmoplastic small round cell tumor) multicenter phase 2 trial

Research output: Contribution to journalResearch articleContributed

Contributors

  • Christoph E Heilig - , National Center for Tumor Diseases (NCT) Dresden (Author)
  • Christoph Heining - , National Center for Tumor Diseases Dresden, National Center for Tumor Diseases (NCT) Dresden, German Cancer Consortium (DKTK) Partner Site Dresden (Author)
  • Editha Gnutzmann - , National Center for Tumor Diseases (NCT) Dresden (Author)
  • Sandra Roldan - , National Center for Tumor Diseases (NCT) Dresden (Author)
  • Laura Heiligenthal - , National Center for Tumor Diseases (NCT) Dresden (Author)
  • Monika Sparber-Sauer - , Department of Pediatric Hematology and Oncology, University Children´s Hospital Tuebingen, Tuebingen, Germany; Klinikum der Landeshauptstadt Stuttgart gKAöR, Olgahospital, Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Pädiatrie 5 (Pädiatrische Onkologie, Hämatologie, Immunologie), Stuttgart, Germany. (Author)
  • Dennis Hahn - , Klinikum Stuttgart (Author)
  • Uta Dirksen - , University Hospital Essen (Author)
  • Rainer Hamacher - , University Hospital Essen, German Cancer Consortium (DKTK) partner site Essen / Düsseldorf (Author)
  • Anne Flörcken - , Charité – Universitätsmedizin Berlin (Author)
  • Anne Thorwarth - , Charité – Universitätsmedizin Berlin (Author)
  • Christoph K W Deinzer - , University Hospital Tübingen (Author)
  • Verena I Gaidzik - , Ulm University Medical Center (Author)
  • Elke Pfaff - , Hopp Children's Cancer Center Heidelberg (KiTZ) (Author)
  • Daniel Hübschmann - , Division of Translational Medical Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany; National Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany; German Cancer Consortium (DKTK), Core Center Heidelberg, Heidelberg, Germany; Computational Oncology Group, Molecular Precision Oncology Program, NCT Heidelberg, Heidelberg, Germany; Innovation and Service Unit for Bioinformatics and Precision Medicine, DKFZ, Heidelb (Author)
  • Karin Arndt - , German Sarcoma Foundation (Author)
  • Stefan M Pfister - , Hopp Children's Cancer Center Heidelberg (KiTZ) (Author)
  • Hanno Glimm - , National Center for Tumor Diseases Dresden, German Cancer Consortium (DKTK) Partner Site Dresden, German Cancer Research Center (DKFZ) - Dresden (Author)
  • Stefan Fröhling - , Division of Translational Medical Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany; National Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany; German Cancer Consortium (DKTK), Core Center Heidelberg, Heidelberg, Germany; Division of Translational Precision Medicine, Institute of Human Genetics, Heidelberg University, Heidelberg, Germany. (Author)
  • Richard F Schlenk - , National Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany; Clinical Trial Center, NCT Heidelberg, Heidelberg, Germany; German Cancer Consortium (DKTK), Core Center Heidelberg, Heidelberg, Germany; Department of Medical Oncology, Heidelberg University Hospital, Heidelberg, Germany; Department of Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany. Electronic address: richard.schlenk@nct-h (Author)

Abstract

BACKGROUND: Desmoplastic small round cell tumor (DSRCT) and synovial sarcoma (SySa) are rare cancers primarily affecting adolescents and young adults. Prognosis is generally poor, particularly upon metastasis, due to limited efficacy of chemotherapies and the lack of molecular mechanism-based approaches. Recently, overexpression of somatostatin receptors (SSTR) 2, 3, and 5 was described in high proportions of DSRCT and SySa. Given the efficacy of somatostatin analogs in other SSTR-expressing malignancies, we will evaluate pasireotide as maintenance therapy in patients with locally advanced or metastatic DSRCT and SySa.

TRIAL DESIGN: PAMSARC (Pasireotide as Maintenance Treatment With Monthly Deep Intramuscular Injection in SSTR2/3/5-Expressing SySa and DSRCT) is an open-label, multicentric, single-arm phase II trial evaluating pasireotide maintenance therapy in adolescents and adults with locally advanced or metastatic SySa or DSRCT who have achieved stable disease or partial response after completion of chemotherapy. Molecular eligibility is determined by SSTR2/3/5 expression via RNA analysis performed within the precision oncology programs MASTER and INFORM. Due to pasireotide's regulatory approval being limited to adults, enrollment follows a "3 + 3 staggered" approach for both adults and adolescents. Treatment consists of pasireotide administered as intragluteal depot injection every 28±3 days. The primary endpoint is progression-free survival; secondary and exploratory analyses include overall survival, patient-reported outcomes, and disease monitoring via liquid biopsies. The sample size calculation assumes exponential data, with 90 % power to detect a hazard ratio of 0.5, requiring 28 participants with an expected 22 events during the study. Sensitivity analyses are planned for both age groups and disease types.

TRIAL REGISTRATION NUMBERS: EUCT: 2024-511935-86-00-00; ClinicalTrials.gov: NCT06456359.

Details

Original languageEnglish
Pages (from-to)100986
JournalCancer treatment and research communications
Volume45
Publication statusE-pub ahead of print - 3 Sept 2025
Peer-reviewedNo

External IDs

Scopus 105015356215
ORCID /0009-0003-2782-8190/work/198593810

Keywords