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

Ovarian Cancer Clinical Trial

Official title:

Randomized Phase II Study of Brostallicin (PNU-166196A) Versus Doxorubicin as First Line Chemotherapy in Patients With Advanced or Metastatic Soft Tissue Sarcoma

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00410462
• Other study ID #: EORTC-62061
• Secondary ID: EORTC-62061EUDRA
• Status: Active, not recruiting
• Phase: Phase 2
• First received: December 11, 2006
• Last updated: August 7, 2014
• Start date: October 2006

Study information

• Verified date: July 2010
• Source: European Organisation for Research and Treatment of Cancer - EORTC
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 118
• Est. primary completion date: September 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Study Design

Allocation: Randomized, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Ovarian Cancer
• Sarcoma
• Small Intestine Cancer

Intervention

Drug:
• brostallicin

• doxorubicin hydrochloride

Locations

Country	Name	City	State
Netherlands	Leiden University Medical Center	Leiden

Sponsors (1)

Lead Sponsor	Collaborator
European Organisation for Research and Treatment of Cancer - EORTC

Country where clinical trial is conducted

Netherlands, 

References & Publications (1)

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 chemother — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Six-month progression-free survival, in terms of complete response, partial response, or no change			No
Secondary	Overall progression-free survival			No
Secondary	Objective tumor response			No
Secondary	Safety (CTCAE v 3.0)			Yes
Secondary	Duration of response			No
Secondary	Overall survival			No