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Search / Trial NCT01884441

Bendamustine, Gemcitabine and Vinorelbine (BeGEV) as Induction Therapy in Relapsed/Refractory Hodgkin's Lymphoma Patients

Launched by ARMANDO SANTORO, MD · Jun 20, 2013

Trial Information

Current as of June 07, 2025

Unknown status

Keywords

Hodgkin Lymphoma Refractory Relapsed

ClinConnect Summary

The aim of this study is to evaluate bendamustine, gemcitabine and vinorelbine (BeGEV) scheme efficacy as induction therapy to high dose chemotherapy with Allogeneic Hematopoietic Stem-Cell Transplantation (AHSCT) for patients with relapsed/refractory Hodglin's Lymphoma (HL).

Four BeGEV courses repeated every 3 weeks in the absence of any reasons listed in the paragraph 7.5; whenever an objective response is observed at disease evaluation performed after IV cycle patients undergo to high dose chemotherapy with AHSCT (conditioning regimens based on preference of each Centre).

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • relapsed/refractory disease after receiving one line of standard chemotherapy
  • history of classical Hodgkin's Lymphoma (HL)
  • Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2
  • at least one site of measurable nodal disease at baseline ≥ 1.5 cm
  • Absolute Neutrophils Count (ANC) ≥ 1.5 x 109/L; Platelets count ≥ 75 x 109/L
  • Exclusion Criteria:
  • Diagnosis of Nodular lymphocyte predominant Hodgkin's lymphoma (NLPHL)
  • prior radiation therapy ≤ 3 weeks prior to start of study treatment
  • any concurrent anti-cancer therapy
  • evidence of another malignancy not in remission or history of such a malignancy within the last 2 years.
  • aspartate aminotransferase (AST/SGOT) and/or alanine aminotransferase (ALT/SGPT) ≥ 2.5 x upper limit of normal (ULN) or ≥ 5.0 x ULN if the transaminase elevation is due to disease involvement
  • known history of Human immunodeficiency virus (HIV)seropositivity
  • hepatitis B virus (HBV) or hepatitis B virus (HCV)active hepatitis

About Armando Santoro, Md

Dr. Armando Santoro is a distinguished clinical trial sponsor with extensive expertise in advancing medical research and innovation. With a robust background in clinical medicine and a commitment to enhancing patient care, Dr. Santoro leads initiatives that focus on developing and evaluating novel therapeutic interventions. His sponsorship emphasizes rigorous scientific methodologies, ethical considerations, and collaborative partnerships, fostering an environment that prioritizes patient safety and data integrity. Through his efforts, Dr. Santoro aims to contribute significantly to the advancement of medical knowledge and the improvement of treatment outcomes across diverse patient populations.

Locations

Rozzano, Mi, Italy

Patients applied

0 patients applied

Trial Officials

Armando Santoro, MD

Principal Investigator

Istituto Clinico Humanitas

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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