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Spots Global Cancer Trial Database for NBTXR3 Crystalline Nanoparticles and Radiation Therapy in Treating Randomized Patients in Two Arms With Soft Tissue Sarcoma of the Extremity and Trunk Wall

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Trial Identification

Brief Title: NBTXR3 Crystalline Nanoparticles and Radiation Therapy in Treating Randomized Patients in Two Arms With Soft Tissue Sarcoma of the Extremity and Trunk Wall

Official Title: A Multicenter Randomized, Open-Label Phase II/III Study, To Compare The Efficacy Of NBTXR3, Implanted As Intratumor Injection And Activated By Radiotherapy, Versus Radiotherapy Alone In Patients With Locally Advanced Soft Tissue Sarcoma Of The Extremity And Trunk Wall

Study ID: NCT02379845

Study Description

Brief Summary: RATIONALE: Radiation therapy given before surgery of soft tissue sarcoma decreases the size of the tumor mass and the presence of malignant cells in its peripheral region. NBTXR3 and radiation therapy may kill more cancer cells and increase the tumor shrinkage rendering surgery more feasible or easier and achieve better local control of the tumor. PURPOSE: This phase II/III is a prospective randomized, multi-center, open-label and active controlled two arms study in patients with locally advanced soft tissue sarcoma (STS) of the extremity and trunk wall. Patients will be randomized to receive either NBTXR3 as intratumor injection, activated by external beam radiation therapy or external beam radiation therapy alone, as preoperative treatment. Once the radiotherapy treatment is completed, tumor surgery will be performed in all patients.

Detailed Description: Patients who will be allocated in arm A, will receive a single intratumor injection of NBTXR3 and will receive external beam radiotherapy starting 24hrs after the injection up to completion of 5 weeks, 5 days a week of treatment (50Gy, 2Gy/fraction). Then, all patients will undergo surgical resection of the tumor 5 weeks later and will be followed for wound healing and toxicity assessment. A visit of end of treatment will take place approximately 3-4 weeks after surgery. Patients will be followed for evaluation of their disease status and adverse event until the end of study.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Capital Region Cancer Service, Canberra Hospital, Canberra, , Australia

Chris O'Brien Lifehouse, Sydney, , Australia

Jules Bordet Institute, Bruxelles, , Belgium

Ghent University Hospital, Ghent, , Belgium

Centre Rene Gauducheau, Nantes, Saint Herblain, France

Institut Bergonie, Bordeaux, , France

Centre Leon Berard, Lyon, , France

Institut Paoli Calmettes, Marseille, , France

Centre Regional de Lutte Contre Le Cancer Paul Lamarque, Montpellier, , France

Centre Antoine Lacassagne, Nice, , France

Institut Curie, Paris, , France

Institut Claudius Regaud - Oncopole, Toulouse, , France

Institut Gustave Roussy, Villejuif, , France

Klinikum Mannheim, Mannheim, , Germany

Klinikum Nürnberg, Nürnberg, , Germany

Princes of Wales Hospital, Shatin, , Hong Kong

Medical Centre, Hungarian Defence Forces, Budapest, , Hungary

National Institute of Oncology, Budapest, , Hungary

University Pècs, Pecs, , Hungary

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, , Italy

Institute of Oncology Veneto IOV, Padova, , Italy

Instituto Nazionale Tumori Regina Elena, Rome, , Italy

Oslo University Hospital, Oslo, , Norway

Perpetual Succour Hospital Cebu, Cebu City, , Philippines

University of Santo Thomas, Manila, , Philippines

The Medical City, Pasig City, , Philippines

St. Luke's Medical Center, Quezon City, , Philippines

Cancer Center Institute, Warsaw, , Poland

Institutul Oncologic Bucuresti, Bucharest, , Romania

Spitalului Universitar de Urgenta Militar Central, Bucharest, , Romania

Amethyst-Cluj, Floresti, , Romania

County Hospital 'Dr Gavril Curteanu', Oradea, , Romania

County Hospital, Targu Mures, Targu Mures, , Romania

Municipal Emergency Hospital, Timisoara, , Romania

Iatros International, Bloemfontein, , South Africa

The Oncology Centre, Durban, , South Africa

Gvi Outeniqua Oncology Unit, George, , South Africa

Wilgers Oncology Centre, Pretoria, , South Africa

Hospital Universitari Vall D'Hebron, Barcelona, , Spain

Hospital Clinico Universitario San Carlos, Madrid, , Spain

START MADRID, Hospital Fundacion Jimenez Diaz, Madrid, , Spain

START MADRID, Hospital Universitario Madrid Norte Sanchinarro, Madrid, , Spain

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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