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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rozzano, Mi, Italy
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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