SHIELD

Trial overview

To evaluate the efficacy and toxicity of VEPEMB in a phase II study in older patients with Hodgkins Lymphoma (HL).  A number of older patients with HL fail to enter clinical trials as they are "not fit" for multiple drug chemotherapy.  This study will aim to include all pathologically eligible patients in participating centres in order to provide a clearer overall clinical picture of this disease, whether or not they undergo protocol chemotherapy.

Inclusion criteria

Histological confirmed classical Hodgkin Lymphoma (HL)

No previous treatment for HL

Age ≥60

 

 

No concomitant neoplasia requiring treatment or known HIV infection

Written informed consent

 

"Non fragile" patient i.e. patient's mental and physical status must be sufficient to withstand the treatment described

Exclusion criteria

Nodular lymphocyte predominance Hodgkin Lymphoma (NLPHL)

Age <60

Patient previously treated for HL

Known HIV infection or concomitant neoplasia

"Fragile patient" or significant abnormality of another system (pulmonary, cardiac, renal and hepatic) which is a contraindication to full dose chemotherapy

Unable to give informed consent

Contact details

Principal Investigator

Dr Rod Johnson

Tel 0113 2068369

Email rod.johnson@leedsth.nhs.uk

Research Nurse

Julie Bagabag

Tel 0113 2068577

Email julie.bagabag@leedsth.nhs.uk



Other trials currently active for Classical Hodgkin Lymphoma

RATHL

A RANDOMISED PHASE III TRIAL TO
ASSESS RESPONSE ADAPTED
THERAPY USING FDG-PET IMAGING
IN PATIENTS WITH NEWLY
DIAGNOSED, ADVANCED HODGKIN
LYMPHOMA

RAPID (PET)

A randomised phase III trial to determine the role of FDG-P imaging in clinical stages IA/IIA Hodgkins disease.


Tags

vepemb hl hd phase ii