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Spots Global Cancer Trial Database for Metronomic Chemotherapy in Elderly Non-fit Patients With Aggressive B-Cell Lymphomas

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Trial Identification

Brief Title: Metronomic Chemotherapy in Elderly Non-fit Patients With Aggressive B-Cell Lymphomas

Official Title: A Phase II Study of Metronomic Chemotherapy in Elderly Non-fit Patients (>65 Years) With Aggressive B-Cell Lymphomas

Study ID: NCT03161054

Study Description

Brief Summary: This is a phase II study of metronomic chemotherapy in elderly non-fit patients (\>65 years) with aggressive B-Cell lymphomas

Detailed Description: Patients eligible for the study will receive 6 courses (q 28 days) of the DEVEC combination, according to the following schedule: * DE: Prednisone (Deltacortene) 25 mg /day will be orally administered from day 1 to day 28 only in cycle 1 From cycle 2 to 6 it is reduced to three times a week (after breakfast, MON, WED, FRI) * V: Vinorelbine 30 mg/day will be orally administered three times a week, 3 week on and 1 week off (after breakfast, MON, WED, FRI). * E: Etoposide 50 mg/day will be orally administered from day 1 to day 14 (before lunch). * C: Cyclophosphamide 50 mg/day will be orally administered from day 1 to day 21 (after dinner). * Rituximab: 375 mg/m2 will be administered by IV infusion up to four infusions on days 8, 15, 22, 29, only in patients suitable for infusion treatment and relapsed after \>6 months from last R-chemotherapy. Refractory patients who had received at least 5 doses of Rituximab will not repeat it during the metronomic therapy. Super-frail patients will not receive etoposide during cycles 1 and 2; etoposide will be included in the treatment schedule starting from cycle 3 at reduced dose (50 mg/day, from day 1 to day 7) only in patients who in cycles 1 and 2 didn't experience hematological toxicity \>G2 and/or non-hematological toxicity \>G1. In Unfit and Frail patients with hemoglobin level at study entry \<11 gr/dL, will start etoposide will be orally administered at reduced dose (50 mg/day from day 1 to day 7). If hemoglobin will raise to ≥11 gr/dL, at subsequent induction cycles etoposide will be administered at full dose (50 mg/day, from day 1 to day 14), As a preventive measure, to avoid perforation, patients with gastrointestinal visceral involvement will receive a pre-phase therapy with steroids (prednisolone 40mg/m2 ) for 6-7 days before starting protocol treatment. Moreover, in these patients the four Rituximab doses will be administered in cycle 2. Patients in CR, CRu, PR and SD after 2 cycles will continue with additional 4 courses. At the end of the induction phase patients in CR, CRu and PR (and also in SD at discretion of local investigator) will continue treatment with maintenance therapy including Vinorelbine, Cyclophosphamide, and Prednisone oral combination to be repeated every 28 days for up to 6 cycles, according to the following schedule: * Cyclophosphamide 50 mg/day will be orally administered from day 1 to day 14 (after dinner). * Vinorelbine 30 mg/day will be orally administered three times a week, 3 week on and 1 week off (after breakfast, MON, WED, FRI). * Prednisone 25 mg/day will be orally administered twice a week (after breakfast, MON, FRI). Patients in CR/CRu at the EOT can continue with a post-maintenance phase at discretion of the local investigator up to 12 months, progression or inacceptable toxicity, according to following schedule: * Vinorelbine 30 mg/day will be orally administered three times a week, 3 week on and 1 week off (after breakfast, MON, WED, FRI). * Prednisone 25 mg/day will be orally administered twice a week (after breakfast, MON, FRI). Patients with evidence of Progressive Disease (PD) at any point will stop treatment.

Eligibility

Minimum Age: 65 Years

Eligible Ages: OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

A.O. Spedali Civili di Brescia - Ematologia, Brescia, , Italy

Ospedale di Castelfranco Veneto - Ematologia, Castelfranco Veneto, , Italy

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (I.R.S.T.) - Ematologia, Meldola, , Italy

Ospedale Guglielmo da Saliceto - U.O.Ematologia, Piacenza, , Italy

Ospedale delle Croci - Ematologia, Ravenna, , Italy

Azienda Ospedaliera Arcispedale Santa Maria Nuova - IRCCS c/o CORE (II piano) - Ematologia, Reggio Emilia, , Italy

AO Sant'Andrea - Ematologia, Roma, , Italy

Nuovo Ospedale Civile di Sassuolo - Day Hospital Oncologico, Sassuolo, , Italy

AOU Senese - U.O.C. Ematologia, Siena, , Italy

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

Contact Details

Name: Francesco Merli, MD

Affiliation: AUSL - IRCCS Arcispedale Santa Maria Nuova viale Risorgimento 80 42123, Reggio Emilia

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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