Evidence map›Paper›PMID 42448612›Full record

Observational studyBritish journal of haematology2026

Real-world outcomes of BrECADD therapy in advanced-stage classical Hodgkin lymphoma: A multicentre retrospective study.

Tzvika Porges, Tsofia Levi, Eldad J Dann, Shlomzion Aumann, Ronit Gurion, Shira Buchrits, Chava Perry, Roy Vitkon, Itai Levi, Ellie Ilan and 17 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Tzvika PorgesInstitute of Hematology, Soroka University Medical Center, Beer Sheva, Israel.ORCID https://orcid.org/0000-0002-3036-3561
Tsofia LeviDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa, Israel.ORCID https://orcid.org/0009-0005-0612-0040
Eldad J DannDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa, Israel.ORCID https://orcid.org/0000-0001-7395-7805
Shlomzion AumannDepartment of Hematology, Hadassah Medical Center and Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Ronit GurionInstitute of Hematology, Davidoff Cancer Center, Rabin Medical Center and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Shira BuchritsInstitute of Hematology, Davidoff Cancer Center, Rabin Medical Center and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Chava PerryDepartment of Hematology, Tel Aviv Sourasky Medical Center and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Roy VitkonDepartment of Hematology, Tel Aviv Sourasky Medical Center and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0001-9843-8817
Itai LeviInstitute of Hematology, Soroka University Medical Center, Beer Sheva, Israel.
Ellie IlanSoroka Clinical Research Center, Beer Sheva, Israel.
Abraham AvigdorDivision of Hematology and Bone Marrow Transplantation, Sheba Medical Center, Tel Hashomer and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Ronit MarcusDivision of Hematology and Bone Marrow Transplantation, Sheba Medical Center, Tel Hashomer and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Reut HarelDepartment of Hematology, Emek Medical Center, Afula, Israel.
Nizar LahhamDepartment of Hematology, Emek Medical Center, Afula, Israel.
May BasoodDepartment of Hematology, Assuta Medical Center, Tel Aviv, Israel.
Kalman FilanovskyHematology Institute, Kaplan Medical Center, Rehovot and Hebrew University, Jerusalem, Israel.
Najib DallyHematology Institute and Blood Bank, Ziv Medical Center and Azrieli Faculty of Medicine, Bar Ilan University, Safed, Israel.
Gilad ItchakiMeir Medical Center, Hematology Institute, Kfar Saba and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Nadav SaridDepartment of Hematology, Edith Wolfson Medical Center and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Noam BenyaminiTzafon Medical Center, Tiberias, Israel.
Sharon Ben BarouchHematology Department, Assuta Medical Center, Ashdod and Ben Gurion University, Beer Sheva, Israel.
Tamar TadmorDivision of Hematology and Blood Bank, Bnai Zion Medical Center and the Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.ORCID https://orcid.org/0000-0002-3435-8612
Orit SoferHematology Department, Hillel Yaffe Medical Center, Hadera, Israel.
Mohamad AboeidDepartment of Hematology and Stem Cell Transplantation, Shaare Zedek Medical Center and Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Ariela StruloviciHematology Department, Shamir Medical Center, Tzrifin, Israel.
Alli OthmanHematology Unit, Galilee Medical Center, Nahariya, Israel.
Meirav KedmiDivision of Hematology and Bone Marrow Transplantation, Sheba Medical Center, Tel Hashomer and Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0001-9175-8551

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced-stage classical Hodgkin lymphoma (cHL) has been traditionally treated with effective chemotherapy regimens, albeit some associated with substantial toxicity. The recently introduced brentuximab vedotin, etoposide, cyclophosphamide, doxorubicin, dacarbazine, dexamethasone (BrECADD) regimen has proved more effective and less toxic than escalated BEACOPP (escBEACOPP: bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone). Our retrospective multicentre study assessed outcomes of this treatment in the real-world setting. It incorporated 100 advanced-stage cHL patients receiving BrECADD at 19 cancer centres between July 2023 and October 2025. The primary end-point was progression-free survival (PFS); secondary end-points included overall response rate (ORR), positron emission tomography (PET)-2 negativity, complete response (CR), overall survival (OS) and toxicity. The median age was 30 (18-65) years; 80% had stage IV disease; 85% had an International Prognostic Score ≥3. ORR and CR were 100% and 95%, respectively; 83% achieved PET-2 negativity, enabling therapy de-escalation from six to four cycles. At a median follow-up of 13.7 months, estimated 1-year PFS and OS were 96% and 100% respectively. Only 4% required radiotherapy. Grade ≥3 neutropenia (83%) and febrile neutropenia (55%) were common; yet, 95% of patients completed all planned cycles. Peripheral neuropathy occurred in 25%, mostly grade 1-2. In this real-world cohort, including high-risk patients, BrECADD demonstrated remarkable efficacy and tolerability, supporting its feasibility and potential to reduce chemotherapy and radiotherapy exposure, while maintaining high treatment efficacy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBrentuximab VedotinHodgkin DiseaseAdolescentAdultAgedBleomycinCyclophosphamideDacarbazineDexamethasoneDoxorubicinEtoposideFemaleHumansMaleMiddle AgedBleomycinBrentuximab VedotinCyclophosphamideDacarbazineDexamethasoneDoxorubicinEtoposideProcarbazineadvanced‐stage Hodgkin lymphomabrentuximab vedotin, etoposide, cyclophosphamide, doxorubicin, dacarbazine, dexamethasone (BrECADD)doxorubicinetoposidePET‐CT‐guided treatmentreal‐world data

Identifiers

PMID42448612
PMCPMC13570145

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.