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Status unknownNCT00410462Updated Aug 8, 2014

Brostallicin or Doxorubicin as First-Line Therapy in Treating Patients With Relapsed, Refractory, or Metastatic Soft Tissue Sarcoma

A Phase 2 interventional study of brostallicin and doxorubicin hydrochloride in Ovarian Cancer, Sarcoma and Small Intestine Cancer, sponsored by European Organisation for Research and Treatment of Cancer - EORTC. Status unknown at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-08-08.

Sponsored by European Organisation for Research and Treatment of Cancer - EORTC · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2010), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
118
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

RATIONALE: Drugs used in chemotherapy, such as brostallicin and doxorubicin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

PURPOSE: This randomized phase II trial is studying the side effects and how well brostallicin or doxorubicin works as first-line therapy in treating patients with relapsed, refractory, or metastatic soft tissue sarcoma.

Read the detailed description

OBJECTIVES:

Primary

  • Determine the activity and safety of brostallicin vs doxorubicin hydrochloride as first-line therapy in patients with relapsed, refractory, or metastatic soft tissue sarcoma.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating and age(younger than 60 years vs 60 years and over). Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive brostallicin IV over 10 minutes on day 1.
  • Arm II: Patients receive doxorubicin hydrochloride IV over 10 minutes on day 1. In both arms, treatment repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed at 30 days and then every 12 weeks thereafter.

PROJECTED ACCRUAL: A total of 108 patients will be accrued for this study.

02

Conditions studied

  • Ovarian Cancer
  • Sarcoma
  • Small Intestine Cancer

Keywords

  • recurrent adult soft tissue sarcoma
  • stage IV adult soft tissue sarcoma
  • adult liposarcoma
  • adult fibrosarcoma
  • adult malignant fibrous histiocytoma
  • adult leiomyosarcoma
  • adult rhabdomyosarcoma
  • adult alveolar soft-part sarcoma
  • adult malignant mesenchymoma
  • adult angiosarcoma
  • adult epithelioid sarcoma
  • adult neurofibrosarcoma
  • adult synovial sarcoma
  • recurrent uterine sarcoma
  • stage IV uterine sarcoma
  • ovarian sarcoma
  • small intestine leiomyosarcoma
  • recurrent small intestine cancer
03

In context

Sarcoma

1,667 studies on the registry are indexed under Sarcoma; 393 are open to participants now.

This study's enrollment of 118 is above the median of 40 across 1,283 interventional studies indexed under Sarcoma.

Browse Sarcoma studies →

Lead sponsor

European Organisation for Research and Treatment of Cancer - EORTC is the lead sponsor of 342 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed high- or intermediate-grade malignant soft tissue sarcoma* of 1 of the following cellular types:

    • Adipocytic (e.g., liposarcoma dedifferentiated, myxoid/round cell, pleomorphic, mixed-type, not otherwise specified)
    • Fibroblastic (e.g., adult fibrosarcoma, myxofibrosarcoma, or sclerosing epithelioid fibrosarcoma)
    • So-called fibrohistiocytic (e.g., pleomorphic malignant fibrous histiocytoma [MFH], giant cell MFH, or inflammatory MFH)
    • Leiomyosarcoma
    • Malignant glomus tumors
    • Skeletal muscle (e.g., rhabdomyosarcoma, alveolar, or pleomorphic)
    • Vascular (e.g., epithelioid hemangioendothelioma or angiosarcoma)
    • Uncertain differentiation (e.g., synovial, epithelioid, alveolar soft part, clear cell, desmoplastic small round cell, extra-renal rhabdoid, malignant mesenchymoma, perivascular epithelioid cell tumor [PEComa], or intimal sarcoma)
    • Malignant peripheral nerve sheath tumors
    • Malignant solitary fibrous tumors
    • Undifferentiated soft tissue sarcomas not otherwise specified
    • Other types of sarcoma if approved by the study coordinator NOTE: *Includes malignant tumors of non-organ origin and skin and uterine leiomyosarcoma
  • The following tumor types are excluded:

    • Embryonal rhabdomyosarcoma
    • Chondrosarcoma
    • Osteosarcoma
    • Ewing tumors/primitive neuroectodermal tumor (PNET)
    • Gastrointestinal stromal tumors
    • Dermatofibrosarcoma protuberans
    • Inflammatory myofibroblastic sarcoma
    • Neuroblastoma
    • Malignant mesothelioma
    • Mixed mesodermal tumors of the uterus
  • Relapsed, refractory, and/or metastatic disease incurable by surgery or radiotherapy
  • Measurable disease
  • Must have formalin fixed paraffin-embedded tumor blocks and representative hematoxylin/eosin slides available for histological central review
  • No symptomatic or known CNS metastases

PATIENT CHARACTERISTICS:

  • At least 60 years of age OR ≥ 18 years of age if patient is not suitable for intensive combination chemotherapy treatments
  • WHO performance status 0-1
  • Absolute neutrophil count > 2,000/mm³
  • Platelet count > 100,000/mm³
  • Bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • AST and ALT ≤ 2.5 times ULN
  • Alkaline phosphatase ≤ 2.5 times ULN
  • Creatinine clearance ≥ 60 mL/min
  • No serious cardiac illness within the past 6 months, including, but not limited to the following:

    • History of documented congestive heart failure
    • High-risk uncontrolled arrhythmias
    • Angina pectoris requiring antianginal medication
    • Clinically significant valvular heart disease
    • Evidence of transmural infarction on ECG
    • Poorly-controlled hypertension (e.g., systolic blood pressure [BP] > 180 mm Hg or diastolic BP > 100 mm Hg)
  • Normal 12-lead ECG
  • LVEF normal by MUGA or echocardiogram
  • No other malignancy within the past 3 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix or breast
  • No other serious and/or unstable medical condition, illness, or lab abnormality that would preclude study participation
  • No psychiatric illness or familial, social, or geographical condition that would preclude study compliance
  • No active uncontrolled infection
  • No known AIDS positivity
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

  • No prior chemotherapy regimen for advanced or metastatic disease (neoadjuvant and adjuvant therapy allowed)
  • No concurrent sargramostim (GM-CSF) except in cases of febrile neutropenia
  • No other concurrent anticancer therapy or investigational agents, including any of the following:

    • Chemotherapy
    • Biological response modifiers
    • Hormone therapy
    • Immunotherapy
  • No other concurrent clinical treatment trial participation
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Enrollment
118 participants (actual)

Interventions

  • Drugbrostallicin
  • Drugdoxorubicin hydrochloride
06

What researchers measure

Primary outcomes

  1. Six-month progression-free survival, in terms of complete response, partial response, or no change

Secondary outcomes

  1. Overall progression-free survival

  2. Objective tumor response

  3. Safety (CTCAE v 3.0)

  4. Duration of response

  5. Overall survival

07

Study locations

1 site
  • Leiden University Medical Center
    Leiden, 2300 RC, Netherlands
08

References and documents

Publications

  • Gelderblom H, Blay JY, Seddon BM, Leahy M, Ray-Coquard I, Sleijfer S, Kerst JM, Rutkowski P, Bauer S, Ouali M, Marreaud S, van der Straaten RJ, Guchelaar HJ, Weitman SD, Hogendoorn PC, Hohenberger P. Brostallicin versus doxorubicin as first-line chemotherapy in patients with advanced or metastatic soft tissue sarcoma: an European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group randomised phase II and pharmacogenetic study. Eur J Cancer. 2014 Jan;50(2):388-96. doi: 10.1016/j.ejca.2013.10.002. Epub 2013 Nov 8. PubMed 24215845 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 8, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00410462
Lead sponsor
European Organisation for Research and Treatment of Cancer - EORTC
Responsible party
Sponsor
First posted
Dec 13, 2006
Start date
Oct 2006
Primary completion
Sep 2008
Last update
Aug 8, 2014

Study contacts

Hans Gelderblom, MD, PhD
study chair · Leiden University Medical Center
View the source record on ClinicalTrials.gov ↗

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