Prevention of Anthracycline-Induced Cardiac Dysfunction With Dexrazoxane in Patients With Diffuse Large-B Cell Lymphoma

NCT ID: NCT06220032

Last Updated: 2026-01-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 324 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-08-15
• Study Completion Date: 2028-12-15

Brief Summary

Patients treated for DLBCL are at high risk of developing AICD. This adverse event is characterized by irreversible damage to the heart muscle with a loss of cardiomyocytes and subsequent decline in cardiac pumping capacity. Thereby patients treated for this malignancy are at double the risk of developing symptomatic heart failure / cardiomyopathy when compared to the general population. This corresponds to a cumulative incidence of 5-10% within 5-years after receiving R-CHOP. In the elderly, an incidence of 26% has been reported after 8-years of follow-up. Among patients who die in complete remission, heart failure has been described to be one of the most important causes of death. ANTICIPATE aims to evaluate if dexrazoxane can prevent AICD in DLBCL patients and identify those at highest risk of AICD. Of all patients treated with anthracyclines in a first-line setting, DLBCL patients were chosen for this trial for two primary reasons. Firstly, these patients have a favourable oncological prognosis with a 5-year relative survival in the Netherlands of 64-78% in those aged 18-74 years increasing the importance of preventing long-term toxicity. Secondly, the cumulative anthracycline dose used for the treatment of DLBCL is higher than the dose used in breast cancer. The cumulative anthracycline dose is the most important risk factor for AICD known.

Detailed Description

HO170 DLBCL-ANTICIPATE: "Prevention of ANThracycline-Induced Cardiac dysfunction by dexrazoxane In PATients with diffusE large B-cell lymphoma" is a national randomized controlled trial that will be conducted across 25 Dutch hospitals. This study will include adult patients with DLBCL in which first-line treatment with 6 cycles of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) is planned (cumulative doxorubicin dose 300 mg/m2). In this trial, we have chosen to include patients with a normal cardiac function before chemotherapy because cardiac dysfunction is a contra-indication for administration of anthracyclines. A total of 324 DLBCL patients will prior to treatment be randomized in a 1:1 ratio to either (1) intravenous dexrazoxane administration in a 10:1 dexrazoxane:doxorubicin ratio prior to each doxorubicin infusion or (2) no cardioprotective treatment (current standard of care). Due to the low pH of the dexrazoxane solution that would jeopardize the blinding no placebo is used. Cardiac function will be screened with echocardiography prior to the initiation of chemotherapy and followed-up at 4- and 12-months post randomization. The primary end point of the study will be the incidence of AICD, defined as a left ventricular ejection fraction (LVEF) decline of ≥10 percentage points from baseline and below 50% (normal reference value for two-dimensional (2D) echocardiography). The secondary endpoint will be the percentage of patients with complete metabolic remission (CMR) after R-CHOP chemotherapy, to reassure that dexrazoxane does not influence the antineoplastic efficacy of doxorubicin. To declare ANTICIPATE successful, the trial must show both the superiority of addition of dexrazoxane on the primary endpoint and non-inferiority on the secondary endpoint. Deep-phenotyping of patient- and treatment-related factors will be performed to evaluate their prognostic value.

Conditions

DLBCL - Diffuse Large B Cell Lymphoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A

Standard R-CHOP 21 treatment regimen:

6 cycles R-CHOP 21 (rituximab*, cyclophosphamide, doxorubicin, vincristine, prednisolone)

*The use of a biosimilar is allowed.

Group Type: EXPERIMENTAL

Rituximab

Intervention Type: DRUG

Day 1 Cycle 1-6: 375 mg/m2 (iv)

Cyclophosphamide

Intervention Type: DRUG

Day 1 Cycle 1-6: 750 mg/m2 (iv)

Doxorubicin

Intervention Type: DRUG

Day 1 Cycle 1-6: 50 mg/m2 (iv)

Vincristine

Intervention Type: DRUG

Day 1 Cycle 1-6: 1.4 mg/m2 (max 2 mg) (iv)

Prednisolone

Intervention Type: DRUG

Day 1-5 Cycle 1-6: 100 mg (oral)

Lenalidomide

Intervention Type: DRUG

Day 1-14 Cycle 1-6: 15 mg day (oral) Only in case of a double hit lymphoma.

Pegfilgrastim

Intervention Type: DRUG

6 mg (1 dose per cycle) in case of neutropenia. Pegfilgastim is mandatory in patients that receive R2-CHOP21.

Arm B -

Addition of the cardioprotectant dexrazoxane to the R-CHOP 21 regimen:

R-CHOP21 (rituximab*, cyclophosphamide, doxorubicin, vincristine, prednisolone plus dexrazoxane).

*The use of a biosimilar is allowed.

Group Type: EXPERIMENTAL

Dexrazoxane

Intervention Type: DRUG

Day 1 Cycle 1-6: Dexrazoxane 500 mg/m2 (iv) will be given 30 minutes before doxorubicin infusion and should be infused during 15 minutes.

Rituximab

Intervention Type: DRUG

Day 1 Cycle 1-6: 375 mg/m2 (iv)

Cyclophosphamide

Intervention Type: DRUG

Day 1 Cycle 1-6: 750 mg/m2 (iv)

Doxorubicin

Intervention Type: DRUG

Day 1 Cycle 1-6: 50 mg/m2 (iv)

Vincristine

Intervention Type: DRUG

Day 1 Cycle 1-6: 1.4 mg/m2 (max 2 mg) (iv)

Prednisolone

Intervention Type: DRUG

Day 1-5 Cycle 1-6: 100 mg (oral)

Lenalidomide

Intervention Type: DRUG

Day 1-14 Cycle 1-6: 15 mg day (oral) Only in case of a double hit lymphoma.

Pegfilgrastim

Intervention Type: DRUG

6 mg (1 dose per cycle) in case of neutropenia. Pegfilgastim is mandatory in patients that receive R2-CHOP21.

Interventions

Dexrazoxane

Day 1 Cycle 1-6: Dexrazoxane 500 mg/m2 (iv) will be given 30 minutes before doxorubicin infusion and should be infused during 15 minutes.

Intervention Type: DRUG

Rituximab

Day 1 Cycle 1-6: 375 mg/m2 (iv)

Intervention Type: DRUG

Cyclophosphamide

Day 1 Cycle 1-6: 750 mg/m2 (iv)

Intervention Type: DRUG

Doxorubicin

Day 1 Cycle 1-6: 50 mg/m2 (iv)

Intervention Type: DRUG

Vincristine

Day 1 Cycle 1-6: 1.4 mg/m2 (max 2 mg) (iv)

Intervention Type: DRUG

Prednisolone

Day 1-5 Cycle 1-6: 100 mg (oral)

Intervention Type: DRUG

Lenalidomide

Day 1-14 Cycle 1-6: 15 mg day (oral) Only in case of a double hit lymphoma.

Intervention Type: DRUG

Pegfilgrastim

6 mg (1 dose per cycle) in case of neutropenia. Pegfilgastim is mandatory in patients that receive R2-CHOP21.

Intervention Type: DRUG

Other Intervention Names

Cardioxane; Revlimid; Pegfilgastim

Eligibility Criteria

Inclusion Criteria

1. Untreated patients with a confirmed histologic diagnosis of CD20+ DLBCL according to WHO classification 2022:

• DLBCL, not otherwise specified (NOS)
• High-grade B-cell lymphoma NOS
• High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 translocation when DA-EPOCH-R is not an option. R2- CHOP is allowed.
• Follicular lymphoma
• T-cell/histiocyte-rich B cell lymphoma (THRBCL)

Note: Transformed, previously untreated lymphoma is allowed.

Note: 5-day treatment of dexamethasone 15 mg/day or prednisone 100 mg/day or local radiotherapy in order to control life-threatening/invalidating tumor related symptoms is allowed.

Note: It is allowed to start with a first cycle of R-CHOP21 pending the FISH results.

2. Planned treatment with 6 R-CHOP21. The following regimens are also allowed:

• Treatment with reversed R-CHOP21
• Treatment with R2-CHOP21 (6 R-CHOP21 + lenalidomide 15 mg day 1-14) in case of double hit lymphoma
• Two additional administrations of rituximab after 6 cycles of R-CHOP21
• High dosis MTX and/or MTX-it for CNS prophylaxis

3. Ann Abor stages II-IV and stage I if the treatment plan is 6 R-CHOP21 in case of bulky disease (defined as a ≥10 cm mass);

4. Age ≥ 18 years;

5. WHO performance status ≤ 2, WHO 3 performance status is allowed when considered directly related to the DLBCL;

6. Negative pregnancy test at study entry for women of childbearing potential;

7. Female patient is either post-menopausal for at least 1 year before the screening visit or surgically sterile or if of childbearing potential, agrees to practice two effective methods of contraception, at the same time, from the time of signing the informed consent through at least 12 months after the last dose of protocol treatment, or agrees to completely abstain from heterosexual intercourse;

8. Male patient, even if surgically sterilized, (i.e., status post vasectomy) agrees to practice effective barrier contraception during the entire study period and through 12 months after the last dose of protocol treatment, or agrees to completely abstain from heterosexual intercourse;

9. Patient is able to adhere to the study visit schedule and other protocol requirements;

10. Written informed consent.

Exclusion Criteria

1. Any of the following B-cell lymphomas according to WHO classification 2022:

o Central Nervous System involvement by DLBCL;

Note: high CNS-IPI is allowed

• Testicular DLBCL;
• Primary mediastinal B-cell lymphoma;
• Epstein-Barr virus (EBV) post-transplant lymphoproliferative disorder;

2. Any prior malignancy or present malignancy other than DLBCL that required or requires systemic therapy. Prior surgery or local radiotherapy is allowed in case the heart has not been exposed.

3. Patients requiring treatment with mini-R-CHOP

4. Pre-existing cardiac disease including:

• LVEF <50% measured with echocardiography (2D or 3D)
• Symptomatic heart failure (NYHA ≥II) or hospitalization for heart failure in the last year;
• Refractory anginal symptoms
• Cardiac arrhythmias not controlled with optimal medical treatment, in case of atrial fibrillation the ventricular response needs to be <110/min;
• Significant valvular dysfunction on echocardiography;
• Non-ischemic cardiomyopathy

5. Non-diagnostic/poor transthoracic echocardiography imaging quality at baseline;

6. Severe pulmonary dysfunction defined as breathlessness at rest (COPD GOLD III or IV), unless clearly related to DLBCL;

7. Severe neurological or psychiatric disease;

8. Inadequate hematological function (absolute Neutrophil Count (ANC) <1.0x109/L or platelets <75x109/L), unless clearly related to DLBCL;

9. Significant hepatic dysfunction (serum bilirubin or transaminases ≥ 3 times the upper limit of normal) unless related to lymphoma infiltration of the liver;

10. Active hepatitis B or C infection (serology testing is required at screening). Patients positive for hepatitis B surface antigen (HBsAg) regardless of antibody status or HBsAg negative but anti-HBc positive are only eligible if HBV-PCR is negative and patients are protected with lamuvidine or entecavir. Patients with positive hepatitis C serology are only eligible if HCV-(RNA) is confirmed negative;

11. Significant renal dysfunction (creatinine clearance < 30 ml/min after rehydration) or requiring dialysis;

12. Active uncontrolled fungal, bacterial and/or viral infection;

13. Patient known to be HIV-positive;

14. Breast-feeding female patients;

15. Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol and follow-up schedule;

16. Participation in another clinical trial with anti-cancer therapy or a cardiovascular drug.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Stichting Hemato-Oncologie voor Volwassenen Nederland

OTHER

Sponsor Role: lead

UMC Utrecht

OTHER

Sponsor Role: collaborator

Amsterdam University Medical Centers

UNKNOWN

Sponsor Role: collaborator

The Dutch Network for Cardiovascular Research (WCN)

UNKNOWN

Sponsor Role: collaborator

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

A. van Rhenen, MD

Role: PRINCIPAL_INVESTIGATOR

UMC Utrecht

M.P.M. Linschoten, MD

Role: PRINCIPAL_INVESTIGATOR

Amsterdam UMC

Locations

NL-Den Bosch-JBZ

's-Hertogenbosch, , Netherlands

Site Status: RECRUITING

NL-Almelo-ZGTALMELO

Almelo, , Netherlands

Site Status: RECRUITING

NL-Amstelveen-AMSTELLAND

Amstelveen, , Netherlands

Site Status: RECRUITING

NL-Apeldoorn-GELREAPELDOORN

Apeldoorn, , Netherlands

Site Status: RECRUITING

NL-Arnhem-RIJNSTATE

Arnhem, , Netherlands

Site Status: RECRUITING

NL-Breda-AMPHIA

Breda, , Netherlands

Site Status: RECRUITING

NL-Delft-RDGG

Delft, , Netherlands

Site Status: RECRUITING

NL-Dordrecht-ASZ

Dordrecht, , Netherlands

Site Status: RECRUITING

NL-Eindhoven-CATHARINA

Eindhoven, , Netherlands

Site Status: RECRUITING

NL-Eindhoven-MAXIMAMC

Eindhoven, , Netherlands

Site Status: RECRUITING

NL-Goes-ADRZ

Goes, , Netherlands

Site Status: RECRUITING

NL-Groningen-MARTINI

Groningen, , Netherlands

Site Status: RECRUITING

NL-Harderwijk-STJANSDALHARDERWIJK

Harderwijk, , Netherlands

Site Status: RECRUITING

NL-Hilversum-TERGOOI

Hilversum, , Netherlands

Site Status: RECRUITING

NL-Hoofddorp-SPAARNEGASTHUIS

Hoofddorp, , Netherlands

Site Status: RECRUITING

NL-Nieuwegein-ANTONIUS

Nieuwegein, , Netherlands

Site Status: RECRUITING

NL-Nijmegen-CWZ

Nijmegen, , Netherlands

Site Status: RECRUITING

NL-Rotterdam-IKAZIA

Rotterdam, , Netherlands

Site Status: RECRUITING

NL-Schiedam-FRANCISCUSVLIETLAND

Schiedam, , Netherlands

Site Status: RECRUITING

NL-Sittard-ZUYDERLAND MC

Sittard, , Netherlands

Site Status: RECRUITING

NL-Sneek-ANTONIUSSNEEK

Sneek, , Netherlands

Site Status: RECRUITING

NL-Den Haag-HAGA

The Hague, , Netherlands

Site Status: RECRUITING

NL-Utrecht-UMCUTRECHT

Utrecht, , Netherlands

Site Status: RECRUITING

NL-Venlo-VIECURI

Venlo, , Netherlands

Site Status: RECRUITING

NL-Zwolle-ISALA

Zwolle, , Netherlands

Site Status: RECRUITING

Countries

Netherlands

Central Contacts

A. van Rhenen, MD

Role: CONTACT

A.vanRhenen@umcutrecht.nl

+31 107041560

M.P.M. Linschoten, MD

Role: CONTACT

m.p.m.linschoten@amsterdamumc.nl

References

Linschoten M, Geels J, van Werkhoven E, Visser-Wisselaar H, Chamuleau MED, Teske AJ, Robbers L, Oerlemans S, Crommelin H, Breems-de Ridder M, Schut A, Asselbergs FW, van Rhenen A; HOVON 170 DLBCL - ANTICIPATE consortium. Rationale and design of the HOVON 170 DLBCL-ANTICIPATE trial: preventing anthracycline-induced cardiac dysfunction with dexrazoxane. Cardiooncology. 2025 Jan 28;11(1):8. doi: 10.1186/s40959-025-00303-y.

Reference Type: DERIVED

PMID: 39875951 (View on PubMed)

Related Links

https://hovon.nl/nl/trials/ho170

HOVON study website

Other Identifiers

2023-505377-32

Identifier Type: OTHER

Identifier Source: secondary_id

HO170 DLBCL-ANTICIPATE

Identifier Type: -

Identifier Source: org_study_id