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

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragen

Beitragende

  • Christoph E Heilig - , Nationales Zentrum für Tumorerkrankungen (NCT) Dresden (Autor:in)
  • Christoph Heining - , Nationales Centrum für Tumorerkrankungen Dresden, Nationales Zentrum für Tumorerkrankungen (NCT) Dresden, Deutsches Konsortium für Translationale Krebsforschung (DKTK) - Dresden (Autor:in)
  • Editha Gnutzmann - , Nationales Zentrum für Tumorerkrankungen (NCT) Dresden (Autor:in)
  • Sandra Roldan - , Nationales Zentrum für Tumorerkrankungen (NCT) Dresden (Autor:in)
  • Laura Heiligenthal - , Nationales Zentrum für Tumorerkrankungen (NCT) Dresden (Autor:in)
  • 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. (Autor:in)
  • Dennis Hahn - , Klinikum Stuttgart (Autor:in)
  • Uta Dirksen - , Universitätsklinikum Essen (Autor:in)
  • Rainer Hamacher - , Universitätsklinikum Essen, Deutsches Konsortium für Translationale Krebsforschung (DKTK) - Essen / Düsseldorf (Autor:in)
  • Anne Flörcken - , Charité – Universitätsmedizin Berlin (Autor:in)
  • Anne Thorwarth - , Charité – Universitätsmedizin Berlin (Autor:in)
  • Christoph K W Deinzer - , Universitätsklinikum Tübingen (Autor:in)
  • Verena I Gaidzik - , Universitätsklinikum Ulm (Autor:in)
  • Elke Pfaff - , Hopp Kindertumorzentrum Heidelberg (KiTZ) (Autor:in)
  • 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 (Autor:in)
  • Karin Arndt - , Deutsche Sarkom-Stiftung (Autor:in)
  • Stefan M Pfister - , Hopp Kindertumorzentrum Heidelberg (KiTZ) (Autor:in)
  • Hanno Glimm - , Nationales Centrum für Tumorerkrankungen Dresden, Deutsches Konsortium für Translationale Krebsforschung (DKTK) - Dresden, Deutsches Krebsforschungszentrum (DKFZ) - Dresden (Autor:in)
  • 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. (Autor:in)
  • 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 (Autor:in)

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

OriginalspracheEnglisch
Seiten (von - bis)100986
FachzeitschriftCancer treatment and research communications
Jahrgang45
PublikationsstatusElektronische Veröffentlichung vor Drucklegung - 3 Sept. 2025
Peer-Review-StatusNein

Externe IDs

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

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