Evidence map›Paper›PMID 39034771›Full record

ArticleCancer science2024

Interim PET-guided ABVD or ABVD/escalated BEACOPP for newly diagnosed advanced-stage classic Hodgkin lymphoma (JCOG1305).

Shigeru Kusumoto, Wataru Munakata, Ryunosuke Machida, Takashi Terauchi, Hiroaki Onaya, Masahiko Oguchi, Shinsuke Iida, Kisato Nosaka, Yasuhiro Suzuki, Yasuhiko Harada and 15 more

Abstract read
In one paragraph

Article in Cancer science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

25 authors.

Shigeru KusumotoDepartment of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan.ORCID https://orcid.org/0000-0001-6546-1279
Wataru MunakataDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4679-0656
Ryunosuke MachidaJCOG Data Center, National Cancer Center Hospital, Tokyo, Japan.
Takashi TerauchiJapanese Foundation for Cancer Research Department of Nuclear Medicine, Cancer Institute Hospital, Tokyo, Japan.
Hiroaki OnayaDepartment of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya, Japan.
Masahiko OguchiRadiation Oncology Department, Cancer Institute Hospital, The Japanese Foundation for Cancer Research, Tokyo, Japan.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0002-4951-960X
Kisato NosakaKumamoto University Hospital, Kumamoto, Japan.ORCID https://orcid.org/0000-0001-6682-2451
Yasuhiro SuzukiDepartment of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Yasuhiko HaradaDepartment of Hematology, Toyota Kosei Hospital, Toyota, Japan.
Kana MiyazakiDepartment of Hematology and Oncology, Mie University School of Medicine, Tsu, Japan.ORCID https://orcid.org/0000-0001-6547-3181
Masaki MarutaDepartment of Hematology, Clinical Immunology and Infectious Diseases, Ehime University Hospital, Toon, Japan.
Noriko FukuharaDepartment of Hematology, Tohoku University School of Medicine, Sendai, Japan.
Tomomi ToubaiDepartment of Internal Medicine III, Division of Hematology and Cell Therapy, Yamagata University Faculty of Medicine, Yamagata, Japan.
Nobuko KubotaDivision of Hematology, Saitama Cancer Center, Ina, Japan.
Ken OhmachiDepartment of Hematology and Oncology, School of Medicine, Tokai University, Isehara, Japan.ORCID https://orcid.org/0000-0002-5530-818X
Toko SaitoDepartment of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan.
Shinya RaiDepartment of Hematology and Rheumatology, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0003-3929-9751
Ishikazu MizunoDepartment of Hematology, Hyogo Cancer Center, Akashi, Japan.
Suguru FukuharaDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2423-9978
Mai TakeuchiDepartment of Pathology, Kurume University, Kurume, Japan.ORCID https://orcid.org/0000-0002-4006-3810
Ukihide TateishiDepartment of Diagnostic Radiology and Nuclear Medicine, Tokyo Medical and Dental University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6548-8698
Dai MaruyamaDepartment of Hematology Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0654-6920
Kunihiro TsukasakiDepartment of Hematology, International Medical Center, Saitama Medical University, Saitama, Japan.
Hirokazu NagaiDepartment of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Funding

Japan Agency for Medical Research and Development 19ck0106509Japan Agency for Medical Research and Development JP16ck0106220National Cancer Center Research and Development Funds 2020-J-3National Cancer Center Research and Development Funds 2023-J-03National Cancer Center Research and Development Funds 25-A-13National Cancer Center Research and Development Funds 26-A-4National Cancer Center Research and Development Funds 29-A-3
6 · The paper itself

Abstract

This single-arm confirmatory study (JCOG1305) aimed to evaluate the utility of interim positron emission tomography (iPET)-guided therapy for newly diagnosed advanced-stage classic Hodgkin lymphoma (cHL). Patients aged 16-60 years with cHL received two cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) and then underwent an iPET scan (PET2), which was centrally reviewed using a five-point Deauville scale. PET2-negative patients continued an additional four cycles of ABVD, whereas PET2-positive patients switched to six cycles of escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (eBEACOPP). The co-primary endpoints were 2-year progression-free survival (PFS) among all eligible and PET2-positive patients. Ninety-three patients were enrolled between January 2016 and December 2019. One patient was ineligible because of a diagnostic error. The median age of the 92 eligible patients was 35 (interquartile range, 28-48) years. Forty (43%) patients had stage III disease, and 43 (47%) had stage IV disease. The remaining nine (10%) patients had stage IIB disease with risk factors. Nineteen PET2-positive (21%) patients received eBEACOPP, 18 completed six cycles of eBEACOPP, 73 PET2-negative (79%) patients continued ABVD, and 70 completed an additional four cycles of ABVD. With a median follow-up period of 41.1 months, the 2-year PFS of 92 eligible patients and 19 PET2-positive patients were 84.8% (80% confidence interval [CI], 79.2-88.9) and 84.2% (80% CI, 69.7-92.1), respectively. Both primary endpoints were met at the prespecified threshold. This study demonstrates that iPET-guided therapy is a useful treatment option for younger patients with newly diagnosed advanced-stage cHL. Registration number: jRCTs031180218.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBleomycinCyclophosphamideDacarbazineDoxorubicinEtoposideHodgkin DiseaseNeoplasm StagingPositron-Emission TomographyPrednisoneProcarbazineVinblastineVincristineAdolescentAdultFemaleBleomycinCyclophosphamideDacarbazineDoxorubicinEtoposidePrednisoneProcarbazineVinblastineVincristineABVDadvanced‐stagecHLescalated BEACOPPinterim PET‐guided

Identifiers

PMID39034771
PMCPMC11447878

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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.