⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for "MIRO" Molecularly Oriented Immuno-radio-therapy

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: "MIRO" Molecularly Oriented Immuno-radio-therapy

Official Title: "MIRO" (Molecularly Oriented Immuno - Radio -Therapy): Multicenter Phase II Study for the Treatment of the Molecular Basis of Stage I / II Follicular Lymphoma With Local Radiotherapy With / Without Ofatumumab

Study ID: NCT02710643

Interventions

OFATUMUMAB

Study Description

Brief Summary: Phase II prospective multicenter study for stage I/II Follicular Lymphoma treated with involved-field radiotherapy (IFRT) at doses of 24 Gy) with or without Ofatumumab for 8 weekly doses on molecular basis. Patients with positive basal Bcl-2 will be followed every 3 months and with Bcl-2 detection every 6 months for 3 years. Patient with negative basal Bcl-2 will be followed every 3 months without further Bcl-2 detection. Ofatumumab treatment will be administered to: 1. Patients with positive basal PCR for Bcl-2-IgH rearrangement in BM and/or PB, resulting still positive after IFRT; 2. Patients with positive basal PCR for Bcl-2-IgH in

Detailed Description: Stage I/IIA follicular lymphoma (FL) is considered a localized disease that can be adequately treated with radiotherapy alone. This strategy is recommended by the guidelines of the "Società Italiana di Ematologia" (SIE) and of the "European Society for Medical Oncology" (ESMO) The accurate definition of the truly localised forms represents a crucial issue in order to ensure an appropriate treatment design for such patients. The characteristic t(14;18) translocation, which leads to the over-expression of the Bcl-2 gene, is found in approximately 85% of FL; cells bearing this translocation can be detected in the peripheral blood (PB) or bone marrow (BM) by polymerase chain reaction (PCR). PCR for the t(14;18) translocation provides a sensitive device to identify the presence of minimal non-Hodgkin lymphoma (NHL) cell contamination. Previous experiences have demonstrated that despite the limited stage, Bcl-2/IgH+ cells can be found at diagnosis in PB and/or BM of the majority of the patients. After treatment with local radiotherapy confined to the involved lymph node(s) only, disappearance of circulating Bcl-2/IgH+ cells in PB and/or BM was demonstrated in approximately 60% of positive patients. Quantitative PCR demonstrated the feasibility of clearing PB and BM Bcl-2+ cells after local irradiation of the primary site of the disease only when the basal number of lymphoma cells was \<1:100 000. Anti-CD20 monoclonal antibody treatment has clearly demonstrated, both alone and in combination with chemotherapy and radiotherapy, a high therapeutic potential in FL. A significant impact of treatment with the anti CD20 monoclonal antibody in reducing the minimal residual disease in FL has been demonstrated in several studies when used as consolidation or during the maintenance phase. No data are currently available concerning the ability of anti-CD20 antibody treatment in reducing the proportion of Bcl-2 positive residual cells after radiotherapy in localized FL. The objective of this study is to take advantage of the therapeutic potential of anti-CD20 monoclonal antibody to reduce or eliminate minimal residual disease in patients with FL in localized stage (I/II) after conventional treatment with local radiotherapy of the involved site(s). The effectiveness of anti-CD20 monoclonal antibody treatment will be determined by the proportion of negativization of residual Bcl-2 positive cells after radiotherapy, evaluated by qualitative and quantitative PCR detection of viable Bcl-2/IgH rearranged cells in PB and/or BM.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Ospedale SS. Antonio e Biagio e Cesare Arrigo, Alessandria, AL, Italy

Ematologia Azienda Ospedaliera Policlinico, Bari, BA, Italy

A.O. Spedali Civili, Brescia, BS, Italy

A.O. Niguarda, Milano, MI, Italy

Azienda Ospedaliera S. Gerardo Di Monza, Monza, Monza Brianza, Italy

Osp. S. Maria delle Croci, Ravenna, RA, Italy

A.O. Bianchi - Melacrino - Morelli, Reggio Calabria, RC, Italy

Polo Pontino, Latina, Roma, Italy

Ospedale di Matera, Matera, , Italy

Area Vasta Romagna e IRST, Meldola (FC), , Italy

Ospedali Riuniti Papardo, Messina, , Italy

Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milano, , Italy

Ospedale S. Raffaele, Milano, , Italy

S.C.D.U Ematologia Azienda Ospedaliero Universitaria Maggiore, Novara, , Italy

U.O. Complessa di Ematologia Ospedale di Parma, Parma, , Italy

IRCCS Policlinico S. Matteo di Pavia, Pavia, , Italy

Ausl Di Piacenza, Piacenza, , Italy

Azienda Ospedaliero Universitaria Pisana U.O. Ematologia, Pisa, , Italy

AO Santa Maria Nuova, Reggio Emilia, , Italy

Ausl Di Rimini, Rimini, , Italy

Ematologia e Trapianto Istituto Regina Elena IFO, Roma, , Italy

Policlinico Umberto I - Università "La Sapienza" - Istituto Ematologia -Dipartimento di Biotecnologie Cellulari ed Ematologia, Roma, , Italy

Ospedale civile DH oncologico, Sassuolo (MO), , Italy

Policlinico Le Scotte Clinica Ematologica, Siena, , Italy

SC Oncoematologia con autotrapianto AO Santa Maria, Terni, , Italy

A.O. Universitaria Citta' Della Salute E Della Scienza Di Torino, Torino, , Italy

A.O.U. Citta della Salute e della Scienza di Torino, Torino, , Italy

Contact Details

Name: Alessandro Pulsoni, MD

Affiliation: Policlinico Umberto I - Università "La Sapienza" - Istituto Ematologia

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: