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Quality of Life in Patients With Non-adipocyte Soft Tissue Sarcoma Under Palliative Chemotherapy or Pazopanib (PazoQoL)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03735758
Recruitment Status : Recruiting
First Posted : November 8, 2018
Last Update Posted : November 8, 2018
Information provided by (Responsible Party):

Brief Summary:

Finding the balance between toxicity and benefit should be the major goal when negotiating about the therapeutic regimen [24]. This becomes nowadays even more important, since there are emerging options in the field of sarcoma therapy. Especially in the palliative treatment of sarcoma patients, knowing that na single drug can provide an overall survival benefit, physicians have to incorporate the patient's preferences and goals in life when consulting them.

The study will allow patients with several types of soff tissue sarcoma to be included. After progression under current therapy, the patient will be randomized in a 1:1 fashion and allocated to either pazopanib or investigator's choice. QoL and other secondary outcome measures will be recorded continuously. The aim of the study is to assess PROs, which should be the primary aim when treating these patients.

Condition or disease Intervention/treatment Phase
Soft Tissue Sarcoma Adult Drug: Pazopanib or chemotherapy Phase 4

Detailed Description:

Primary objectives

• Assess the overall quality of life (QoL) under treatment with pazopanib or physician-preferred chemotherapy after 9 weeks

Secondary objectives

  • Assess the overall QoL under treatment with pazopanib compared with the physician's preference of chemotherapy three times in Cycle 1 and Cycle 3 (corresponding to Weeks 1, 2, 3 and 7, 8, 9, respectively)
  • lntergroup evaluation of pain as a main symptom in patients with STS

    • Intergroup evaluation of fatigue and its different categories (physical, mentaf, cognitive, emotional)
    • lntergroup evaluation of anorexia/cachexia as marker tor health related quality of life
    • lntergroup evaluation of satisfaction with care
    • Evaluation of the association of QoL with criteria of response
    • Evaluation of the EORTC QLC-C30 of all patients during FU lntergroup evaluation of treatment effects on survival
  • Evaluation of the prediction of severe eariy toxicity in elderly patients receiving palliative therapy
  • Safety and efficacy of the different treatment regimens

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 150 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: multicentric, controlled, randomized, open Label, parallel-group, prospective
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Quality of Life in Patients With Non-adipocyte Soft Tissue Sarcoma Under Palliative Chemotherapy or Pazopanib — a Randomized, Controlled Trial
Actual Study Start Date : November 2, 2018
Estimated Primary Completion Date : June 30, 2020
Estimated Study Completion Date : December 31, 2022

Resource links provided by the National Library of Medicine

Drug Information available for: Pazopanib

Arm Intervention/treatment
Active Comparator: Arm A
Pazopanib; 800 mg; daily; oral
Drug: Pazopanib or chemotherapy
Randomisation: Arm A /Arm B

Active Comparator: Arm B
Guideline-conform chemotherapy; according SmPCs
Drug: Pazopanib or chemotherapy
Randomisation: Arm A /Arm B

Primary Outcome Measures :
  1. Patient reported outcome [ Time Frame: 9 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • The informed consent form must be signed before any study specific tests or procedures are done
  • Male or female patients aged 18 years and older at the first screening visit
  • Histologically confirmed diagnosis of advanced or metastatic non adipocyte SIS
  • Suitable for treatment with pazopanib in an in-label prescription
  • Patients with a life expectancy of at least 6 months
  • ECOG performance status 0-2
  • Adequate organ function as given in Table 1
  • For patients with previous anthracycline therapy a normal heart function needs to be documented with an LVEF of minimal 50% (echocardiogram)
  • Patients must be willing and able to fill in the QoL questionnaires using a tablet PC
  • Ability to understand and follow study-related instructions
  • Confirmation of the subject's health insurance coverage prior to the first visit

Exclusion Criteria:

  • Pretreatment with pazopanib
  • Contraindications according to the local SmPC of Votrient®
  • Patients having to following STS specific tumors

    • adipocyte sarcoma including all subtypes,
    • all rhabdomyosarcoma, which are not alveolar or pleomorph
    • Chondrosarcoma
    • Osteosarcoma
    • Ewing-tumors, i.e. primitive neuroectodermal tumors (PNET), GIST
    • Dermatofibrosarcoma protuberans
    • lnflammatory myofibroblastic sarcoma
    • Malignant mesotheliom
    • Mesodermal tumors of the Uterus Other malignant underlying diseases with the exception of the following:
    • Free of disease for at least 3 years
    • Completely resected, non-melanoma skin cancer
    • Successfully treated carcinoma in situ
    • Patients with metastases of the central nervous system (CNS) at screening, which are asymptomatic AND do not require treatment with steroids or enzyme-inducing anticonvulsant drugs
    • Patients with metastases of the CNS, which are already treated (operation and/or radiotherapy, radiosurgery or gamma-knife)
  • Major surgery or trauma within 28 days before the first dose of study medication and / or presence of a non-healing wound, fracture, or ulcer
  • Clinical indications of an active bleeding or a bleeding diathesis
  • Known endobronchial lesions or lesions that infiltrate the large pulmonary artery
  • Hemoptysis of> 2.5 mL within 8 weeks before the first dose of study drug
  • Existing uncontrolled infection
  • Heart rate-corrected QT-time according to the Fridericia's-formula (QTcF) 450 ms in males and 460 ms in females
  • History of one or more of the following cardiovascular diseases within the last 6 months:

    • Cardiac angioplasty or coronary stent
    • Myocardial infarction
    • Unstable angina pectoris
    • Coronary artery bypass surgery
    • Symptomatic peripheral arterial disease
  • Cardiac insufficiency NYHA functional dass III or IV
  • Poorly controlled hypertension defined as systolic blood pressure 140 mmHg or diastolic blood pressure 90 mmHg
  • History of cerebrovascular disease, including transient ischemic attacks (TIA), pulmonary embolism or untreated deep vein thrombosis within 6 months prior to study entry. Patients with deep vein thrombosis who have received therapeutic anticoagulation for a minimum of 6 weeks might be included in the study.
  • Clinically significant gastrointestinal changes that increase the risk of gastrointestinal bleeding
  • Clinically significant gastrointestinal changes that may affect the absorption of the study drugs
  • Treatment with any of the following anti-neoplastic therapies:

    • Irradiation or Tumor embolization within 14 days prior to the first dose of study drug
    • Chemotherapy, immunotherapy, biological therapy, study medication or hormonal therapy within 14 days or 5 half lives of substance (whichever is langer) prior to the first dose of study drug
  • If the discontinuation of prohibited medication (see Section 6.9) at least 14 days or 5 half-lives of substance (whichever is langer) prior to the first dose of pazopanib is medically not acceptable or refused by the patient
  • A history of hypersensitivity to any of the study drugs or their ingredients or to drugs with similar chemical structure
  • Addiction or other diseases that preclude the patient from appropriately assessing the nature and scope as well as possible consequences of the clinical trial
  • Pregnant or breast-feeding women
  • Women of childbearing potential unless women who meet the following criteria:

    • Post-menopausal (12 months natural amenorrhea without any application of a hormonal contraceptive or hormonal substitution therapy))
    • Postoperatively (6 weeks after bilateral ovariectomy with or without hysterectomy)
    • Regular and correct use of a contraceptive method with error rate <1% per year such as implants, depot injections, oral contraceptives or intrauterine devices during treatment and up 6 months after end of treatment
    • Sexual abstinence
    • Vasectomy of the partner
  • Men of sexual activity with women of childbearing potential who are not willing to use an effective barrier method of contraception during and up to 6 months after the end of therapy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03735758

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Contact: Katrin Linke, Dr. +49 (0) 351 25933 176
Contact: Carsta Köhler, Dr.

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Sarkomzentrum Berlin-Brandenburg Recruiting
Bad Saarow, Germany, 15526
Principal Investigator: Daniel Pink, Dr.         
Universitätsklinikum Dresden Recruiting
Dresden, Germany, 01307
Principal Investigator: Stephan Richter, Dr.         
Uniklinik Frankfurt Not yet recruiting
Frankfurt, Germany, 60590
Principal Investigator: Marit Ahrens, Dr.         
Uniklinikum Heidelberg Recruiting
Heidelberg, Germany, 69120
Principal Investigator: Gerlinde Egerer, Prof.         
Universitätsklinikum Mannheim Recruiting
Mannheim, Germany, 68167
Principal Investigator: Bernd Kasper, Prof.         
Uniklinik Großhadern Recruiting
München, Germany, 81377
Principal Investigator: Lars Lindner, Prof.         
Universitätsklinik der Paracelsus Privatuniversität Nürnberg Not yet recruiting
Nürnberg, Germany, 90419
Principal Investigator: Marinela Augustin, Dr.         
Sponsors and Collaborators
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Principal Investigator: Markus Schuler, Dr. HELIOS Klinikum Emil von Behring

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Responsible Party: GWT-TUD GmbH Identifier: NCT03735758     History of Changes
Other Study ID Numbers: PazoQoL
First Posted: November 8, 2018    Key Record Dates
Last Update Posted: November 8, 2018
Last Verified: November 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by GWT-TUD GmbH:
in-label prescription
Quality of Life

Additional relevant MeSH terms:
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Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type