High-dose Chemotherapy and Stem Cell Transplantation, in Patients PET-2 Positive, After 2 Courses of ABVD and Comparison of RT Versus no RT in PET-2 Negative Patients

NCT00784537 — Phase 2 / Phase 3, Completed, 520 participants, Fondazione Italiana Linfomi - ETS

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Early Salvage With High Dose Chemotherapy and Stem Cell Transplantation in Advanced Stage Hodgkin's Lymphoma Patients With Positive PET After Two Courses of ABVD (PET-2 Positive) and Comparison of RT Versus no RT in PET-2 Negative Patients

RegistryNCT00784537, acronym HD0801
StatusCompleted
PhasePhase 2 / Phase 3
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment520 (Actual)
SponsorFondazione Italiana Linfomi - ETS (Other); collaborators: Centro di Riferimento per l'Epidemiologia e la Prev. Oncologica Piemonte
ConditionsHodgkin's Lymphoma
InterventionsABVD, ABVD and Radiotherapy (Drug)
Datesstart 2008-09-01, primary completion 2015-01-01, completion 2016-01-01, first posted 2008-11-04, last updated 2018-02-08
Locations27 sites in Italy

Related Papers Related Patents Related Grants Related Experts
All trials for Hodgkin's Lymphoma All trials of ABVD All trials of ABVD and Radiotherapy

-Summary

The purpose of this study is to define an improvement in patients:

* To evaluate if patients resistant to the initial treatment for residual PET-positive masses after the first two courses of ABVD (PET-2 positive), can be salvaged by early shift to high-dose chemotherapy supported by stem cell rescue
* To analyse if patients achieving early complete response (PET-2 negative), can be spared the adjuvant radiotherapy on areas of initial bulky disease, at the end of the planned six courses of ABVD. To answer this question, PET-2 negative patients will be randomized between radiotherapy versus no radiotherapy at the end of ABVD therapy.

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+Detailed description

This study is composed by two phases:

1. A phase II multi-centre study evaluating in patients with advanced stage Hodgkin lymphoma the efficacy of an early salvage treatment with high-dose chemotherapy followed by stem cell transplantation in patients FDG-PET positive after two courses of ABVD (PET-2 positive).
2. A phase III randomised study comparing the efficacy of radiotherapy to the areas of initial bulky disease versus no further therapy in PET-2 negative patients in complete remission (PET-6 negative) at the end of six courses of ABVD.

+Arms and interventions

ArmTypeInterventionsDescription
Arm AOtherDrug: ABVDTwo courses of ABVD. Early restaging with FDG-PET scan (PET-2) The subsequent treatment will be as it follows: * PET-2 positive patients will be high-dose salvage treatment; * PET-2 negative patients will be treated with four additional courses of ABVD (for a total of six courses). The following restaging procedures are planned as it follows: * Optional: Whole body CT scan after the fourth course of ABVD; no therapy change will be made according to CT scan. * Mandatory: Whole body CT and FDG-PET scans after the sixth course of ABVD (PET-6). PET-6 negative patients will be randomized to first arm: No radiotherapy.
Arm BOtherDrug: ABVD and RadiotherapyTwo courses of ABVD. Early restaging with FDG-PET scan (PET-2) The subsequent treatment will be as it follows: * PET-2 positive patients will be high-dose salvage treatment; * PET-2 negative patients will be treated with four additional courses of ABVD (for a total of six courses). The following restaging procedures are planned as it follows: * Optional: Whole body CT scan after the fourth course of ABVD; no therapy change will be made according to CT scan. * Mandatory: Whole body CT and FDG-PET scans after the sixth course of ABVD (PET-6). PET-6 negative patients will be randomized to second arm: Adjuvant radiotherapy (30 Gy) on sites of initial bulky disease.
  • ABVD (Drug): ABVD courses are scheduled every 28 days: Doxorubicin 25 mg/m2 i.v. day 1 and 15 Bleomycin 10 mg/m2 i.v. day 1 and 15 Vinblastine 6 mg/m2 i.v. day 1 and 15 Dacarbazine 375 mg/m2 i.v. day 1 and 15 ABVD courses are scheduled every 28 days: Doxorubicin 25 mg/m2 i.v. day 1 and 15 Bleomycin 10 mg/m2 i.v. day 1 and 15 Vinblastine 6 mg/m2 i.v. day 1 and 15 Dacarbazine 375 mg/m2 i.v. day 1 and 15 Randomization to Arm A (Observation)
  • ABVD and Radiotherapy (Drug): ABVD courses are scheduled every 28 days: Doxorubicin 25 mg/m2 i.v. day 1 and 15 Bleomycin 10 mg/m2 i.v. day 1 and 15 Vinblastine 6 mg/m2 i.v. day 1 and 15 Dacarbazine 375 mg/m2 i.v. day 1 and 15 Randomization to Arm B, Radiotherapy, in patients in CR, on the area of initial bulky disease (see above for the definition of nodal and/or mediastinal bulk).

+Outcome measures

Primary outcomes

  • To evaluate if patients resistant to the initial treatment for residual PET-positive masses after the first two courses of ABVD (PET-2 positive), can be salvaged by early shift to high-dose chemotherapy supported by stem cell rescue. [4 years]

Secondary outcomes

  • To analyse if patients achieving early complete response (PET-2 negative), can be spared the adjuvant radiotherapy on areas of initial bulky disease, at the end of the planned six courses of ABVD. [4 years]

+Eligibility

Sex: All, ages: 18 Years to 70 Years

Inclusion Criteria:

* Histologically confirmed Hodgkin's lymphoma of the classical type (nodular lymphocyte predominance excluded).
* Stage IIB-IV.
* Age 18-70.
* No prior therapy for Hodgkin's lymphoma
* Written informed consent.
* ECOG performance status grades 0-3 (see Appendix E).
* FDG-PET scan before the initiation of treatment.

Exclusion Criteria:

* Prior therapy for Hodgkin's lymphoma.
* Age less than 18 or more than 70.
* Other concomitant or prior malignancies, except basal cell skin carcinoma, or adequately treated carcinoma in situ of the cervix, or any cancer in complete remission for more than 5 years.
* HIV infection.
* Pregnancy or breast-feeding.
* Renal failure (creatinine ≥2 times the normal value), liver failure (AST/ALT or bilirubine ≥ 2.5 times the normal value) or heart failure (NYHA class ≥ 2 or FEV < 45%).

+Locations (27)

FacilityCityCountryStatus
Centro di riferimento Oncologico Oncologia Medica AAvianoItaly
Università Policlinico di Bari - Divisione di Medicina ABariItaly
Policlinco Sant'Orsola Isituto di Ematologia ed oncologia MedicaBolognaItaly
Sezione di Ematologia Spedali CiviliBresciaItaly
Ospedale di Circolo SC Oncologia Medica IIIBusto ArsizioItaly
Divisione di Ematologia Osp.BusincoCagliariItaly
Policlinico Careggi Cattedra di EmatologiaFlorenceItaly
ASLTO4IvreaItaly
Osp. Cardinale Panico Divisione di Ematologia TricaseLecceItaly
Ospedale Niguarda Cà GrandaMilanItaly
Università Avogadro Divisione di EmatologiaNovaraItaly
Ospedale San Francesco UO Ematologia e Centro TrapiantiNuoroItaly
Fondazione Policlinico San Matteo Clinica EmatologicaPaviaItaly
Osp. Santa Maria delle Croci UO EmatologiaRavennaItaly
Ospedale Bianchi Melacrino MorelliReggio CalabriaItaly
Osp. degli Infermi Divisione di OncologiaRiminiItaly
Istituto Regina Elena IFO SC EmatologiaRomaItaly
Osp.Sant'Eugenio Divisione di EmatologiaRomaItaly
Università La Sapienza Dipartimento di Biotecnnologie CellulariRomaItaly
Istituto Clinico Humanitas Divisione di Oncologia Medica ed EmatologiaRozzano (MI)Italy
AO Universitaria di SassariSassariItaly
Policlinico Le ScotteSienaItaly
Struttura Complessa di Onco-EmatologiaTerniItaly
IRCC Onco-Ematologia CandioloTorinoItaly
Osp. San Giovanni Battista_Molinette Ematologia 2TorinoItaly
Azienda Ospedaliero universitaria di UdineUdineItaly
ASL 14 UO OncologiaVerbaniaItaly

+Publications

  • Results publication: Kreuzberger N, Goldkuhle M, von Tresckow B, Kobe C, Sickinger MT, Monsef I, Skoetz N. Positron emission tomography-adapted therapy for first-line treatment in adults with Hodgkin lymphoma. Cochrane Database Syst Rev. 2025 Mar 26;3(3):CD010533. doi: 10.1002/14651858.CD010533.pub3. PMID 40135712
  • Results publication: Ricardi U, Levis M, Evangelista A, Gioia DM, Sacchetti GM, Gotti M, Re A, Buglione M, Pavone V, Nardella A, Nassi L, Zanni M, Franzone P, Frezza GP, Pulsoni A, Grapulin L, Santoro A, Rigacci L, Simontacchi G, Tani M, Zaja F, Abruzzese E, Botto B, Zilioli VR, Rota-Scalabrini D, Freilone R, Ciccone G, Filippi AR, Zinzani PL. Role of radiotherapy to bulky sites of advanced Hodgkin lymphoma treated with ABVD: final results of FIL HD0801 trial. Blood Adv. 2021 Nov 9;5(21):4504-4514. doi: 10.1182/bloodadvances.2021005150. PMID 34597375
  • Results publication: Zinzani PL, Broccoli A, Gioia DM, Castagnoli A, Ciccone G, Evangelista A, Santoro A, Ricardi U, Bonfichi M, Brusamolino E, Rossi G, Anastasia A, Zaja F, Vitolo U, Pavone V, Pulsoni A, Rigacci L, Gaidano G, Stelitano C, Salvi F, Rusconi C, Tani M, Freilone R, Pregno P, Borsatti E, Sacchetti GM, Argnani L, Levis A. Interim Positron Emission Tomography Response-Adapted Therapy in Advanced-Stage Hodgkin Lymphoma: Final Results of the Phase II Part of the HD0801 Study. J Clin Oncol. 2016 Apr 20;34(12):1376-85. doi: 10.1200/JCO.2015.63.0699. Epub 2016 Feb 16. PMID 26884559

+Investigators