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Trial · Interventional

RecruitingPhase 2Registry data

Pasireotide as Maintenance Treatment in Synovial Sarcoma and Desmoplastic Small Round Cell Tumor

Short name PAMSARC

Overview

Status
Recruiting
Phase
Phase 2
Enrollment
28 participants (estimated)
Sponsor
University Hospital Heidelberg · Other
Design
Allocation not applicable · Open label (no masking)
Countries
1 country

Germany

Start
19 Dec 2024
Primary completion
Oct 2027 (estimated)
Completion
Oct 2028 (estimated)
First posted
13 Jun 2024
Last update posted
13 Jan 2025
Conditions
Desmoplastic Small Round Cell Tumor · Synovial Sarcoma

Timeline

1 trial · 1 ongoing

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202420252026202720282029
  1. Ph 2

    PAMSARC

    NCT06456359

    19 Dec 2024 to est. Oct 2028

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

PAMSARC is a non-commercial interventional Phase 2 clinical trial of academic research institutions, with its primary goal being to improve medical treatment of fusion driven Desmoplastic small round cell tumor (DSRCT) and Synovial sarcoma (SySa) in young adults and adolsecents with male predominance. Current management of DSRCT and SySa includes chemotherapy, radiation and aggressive cytoreductive surgery. Despite advances in multimodal therapy, outcomes remain poor with frequent disease recurrence and very limited options for patients with advanced disease. Selected somatostatin receptor (SSTR) family members, i.e., SSTR2, SSTR3 and SSTR5, are frequently overexpressed in DSRCT and SySa, providing the rationale for treatment with somatostatin analogues (SSA). Pasireotide is a SSA with high affinity for SSTR1, -2, -3, and -5 and is approved for the treatment of Cushing's disease and acromegaly and has also shown activity in other cancers. In patients with advanced stage DSRCT and SySa, conventional chemotherapeutic approaches frequently lead to disease response, however, the duration of progression-free time after chemotherapy is short. The targeted approach with pasireotide after initial intensive multimodal treatment may have the potential to significantly improve outcome.

Interventions

  • SigniforDrug

Arms1

  • Experimental

    Pasireotid treatment single arm

    Adults receive 60 mg via intragluteal depot injection every 28±3 days, adolescents 60 mg (body surface area \[BSA\] \>1.6 m²) or 40 mg (BSA 1.1-1.6 m2) via intragluteal depot injection every 28±3 days.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. progression-free survival (PFS)

    Time frame · PFS, measured from study registration to radiologically confirmed disease progression according to Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1, or death from any cause, whichever occurs first up to 4 years

    Registry description

    Assessment of clinical efficacy of pasireotide maintenance therapy

Secondary outcomes(1)
  1. overall survival (OS)

    Time frame · OS, measured from study registration to death from any cause (censoring of patients without an event at date of last follow-up) up to 4 years

    Registry description

    Assessment of clinical efficacy of pasireotide maintenance therapy

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

A trial that is still running, or that stopped early, may post results later.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

More studies

1 study on this page

Indexing hint: Clinical trial · 2025

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.

Heilig et al. 2025Cancer treatment and research communicationscited by 1

PMID 40934647DOI 10.1016/j.ctarc.2025.100986PUB-40934647

Full text at the publisher
Publisher page

Eligibility

Who could join, as posted.

Sex
All
Age
from 13 Years up to 50 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: Patients meeting all of the following criteria are considered for enrolment into the trial: 1. Reference pathological proven diagnosis of DSRCT in any stage; or Reference pathological proven diagnosis of SySa, IRS III, metastatic or relapsed disease 2. High SSTR2/3/5 mRNA expression, as determined by RNA sequencing in the DKFZ/NCT/DKTK MASTER (ClinicalTrials.gov ID: NCT05852522) or INFORM programs. 3. Stable disease, partial or complete response after completion of standard treatment 4. Age from 13 to 50 years 5. For patients (≥16 years): Karnofsky-Index ≥ 80% For patients (\<16 years): Lansky-Index ≥ 80% 6. No curative treatment option 7. Bodyweight ≥ 30kg and BSA ≥ 1.1m² 8. Time from last chemotherapy (at least 2 chemotherapy cycles) to enrollment \<8 weeks 9. Ability of patient to understand character and individual consequences of the clinical trial 10. Written informed consent (for individuals \<18 years of age an ICF for adolescents and their parents is needed) 11. For women of childbearing potential negative urine pregnancy test at screening as well as highly effective forms of contraception have to be in place thereafter * Evidence of childbearing potential is defined as fertile, following menarche and until becoming post-menopausal unless permanently sterile * Postmenopausal or evidence of non-childbearing status is defined as: * Amenorrhea for 1 year or more without an alternative medical cause following cessation of exogenous hormonal treatments plus follicle stimulating hormone (FSH) levels in the postmenopausal range in women not using hormonal contraception or hormonal replacement therapy. * Chemotherapy-induced menopause * Surgical sterilization (bilateral oophorectomy, bilateral salpingectomy, total hysterectomy or tubal ligation at least 6 weeks before IMP treatment) * A man is considered fertile after puberty unless permanently sterile by bilateral orchidectomy 12. Female patients of childbearing potential and male patients with partners of childbearing potential who are sexually active must agree to the use of two forms of contraception in combination (male condom and one highly effective method). These should be started immediately after signing the informed consent form and continued throughout the period of study treatment plus 3 months for female and male patients . Male patients should refrain from fathering a child or donating sperm during the trial and for at least 3 months following the last dose. 13. Adequate bone marrow, renal, and hepatic function defined by laboratory tests within 14 days prior to study treatment: * Hemoglobin ≥ 10 g/dl * Neutrophil count ≥ 1,500/mm3 * Platelet count ≥ 100,000/µl * Bilirubin ≤ 1.5 x upper limit of normal (ULN) * ALT and AST ≤ 2.5 x ULN * Alkaline phosphatase ≤ 2.5 x ULN * PT-INR/PTT ≤ 1.5 x ULN * Albumin ≥ 25 g/l * Creatine kinase ≤ 2.5 x ULN * Serum creatinine \< or = 1.5 mg/dl or creatinine clearance = or \> 51 ml/min (calculation according to Crockroft-Gault) Exclusion Criteria: Patients presenting with any of the following criteria are not included in the trial: 1. History of hypersensitivity to the investigational medicinal product or to any drug with similar chemical structure or to any excipient present in the pharmaceutical form of the investigational medicinal product 2. Concurrent or previous treatment within 30 days in another interventional clinical trial / Participation in other ongoing clinical trials. 3. Uncontrolled concurrent disease, in particular diabetes mellitus 4. Bleeding disorder 5. Therapeutic anticoagulation which cannot be paused temporarily in order to ensure safe intramuscular injection 6. Is taking or requiring any of the prohibited medication listed in Table 5 (6.4.2) 7. Heart rate at rest \< 60/min 8. fasting glucose level \> 110mg/dl 9. Severe neurologic or psychiatric disorder 10. Pregnancy/lactation 11. Prior treatment with somatostatin analog \-

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