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Prognosis of Patients With Relapsed/Refractory Hodgkin Lymphoma Treated With IGEV Induction Therapy Before HDCT With AHSCT (IIL-ProHLRec)

F

Fondazione Italiana Linfomi - ETS

Status

Completed

Conditions

Hodgkin's Lymphoma

Study type

Observational

Funder types

Other

Identifiers

NCT01478191
30
IIL-ProHLRec

Details and patient eligibility

About

This is a retrospective analysis of a homogeneous cohort of patients with relapsed/refractory HL that received IGEV scheme as induction therapy to HDCT and AHSCT for reassess the most common prognostic factors and try to identify a prognostic score with clinical and therapeutic relevance by using 6 clinical tools:

  1. B symptoms(yes/no)
  2. relapse in previously irradiated areas(yes/no)
  3. Ann Arbor Stage (III/IV vs I/II)
  4. disease status at accrual (refractory vs relapsed)
  5. Early relapse within 12 months of Complete Response (CR) versus late relapse after Complete Response (CR) lasting > l2 months",
  6. extranodal involvement (yes/no).

Enrollment

495 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with a history of classical HL relapsed/refractory which received IGEV regimen as induction therapy before high dose chemotherapy with AHSCT
  • Age >18 years
  • Patients with relapsed/refractory disease after standard treatments (chemotherapy +/- radiotherapy) before IGEV induction regimen. (Relapsed = disease relapse after CR.

Refractory = non CR with last chemotherapy line, or progression during last treatment, or disease progression within three months from previous treatment completion).

  • Availability of clinical data, laboratory values and CT scan results of patients enrolled, performed from diagnosis to the last follow-up
  • Patient scheduled to receive three or four IGEV cycles as pretransplantation induction regimen.
  • First IGEV course started before December 31st 2007
  • Assessment of tumor response by Cheson 1999 criteria 11

Exclusion criteria

  • NONE

Trial contacts and locations

40

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Data sourced from clinicaltrials.gov

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