Evidence map›Paper›PMID 31620815›Full record

Trial reportAnnals of hematology2019

Daratumumab plus bortezomib, melphalan, and prednisone in East Asian patients with non-transplant multiple myeloma: subanalysis of the randomized phase 3 ALCYONE trial.

Tomoaki Fujisaki, Takayuki Ishikawa, Hiroyuki Takamatsu, Kenshi Suzuki, Chang-Ki Min, Jae Hoon Lee, Jianping Wang, Robin Carson, Wendy Crist, Ming Qi and 1 more

Open access · hybridAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Annals of hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Observational
  4. Review
  5. Review
  6. [Progress in the treatment of multiple myeloma with daratumumab].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2021
    Article
  7. Article
  8. Review
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

11 authors at 8 institutions in 3 countries.

Tomoaki FujisakiDepartment of Internal Medicine, Matsuyama Red-Cross Hospital, Ehime, Japan.
Takayuki IshikawaDepartment of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan.
Hiroyuki TakamatsuHematology/Respiratory Medicine, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
Kenshi SuzukiDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.
Chang-Ki MinSeoul St. Mary's Hospital, Seoul, South Korea.
Jae Hoon LeeGachon University Gil Medical Center, Incheon, South Korea.
Jianping WangJanssen Research & Development, Raritan, NJ, USA.
Robin CarsonJanssen Research & Development, Spring House, PA, USA.
Wendy CristJanssen Research & Development, Spring House, PA, USA.
Ming QiJanssen Research & Development, Spring House, PA, USA.
Koji NagafujiDivision of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan. knagafuji@med.kurume-u.ac.jp.
Janssen (United States) · USGachon University Gil Medical Center · KRJapanese Red Cross Medical Center · JPKanazawa University · JPKobe City Medical Center General Hospital · JPKurume University · JPMatsuyama Red Cross Hospital · JPSeoul St. Mary's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the ALCYONE trial, daratumumab plus bortezomib, melphalan, and prednisone (D-VMP) reduced the risk of disease progression or death by 50% versus bortezomib, melphalan, and prednisone (VMP) in patients with transplant-ineligible newly diagnosed multiple myeloma. Here, we report a subanalysis of East Asian patients from ALCYONE. After a median follow-up of 17.1 and 15.9 months for Japanese (n = 50) and Korean (n = 41) patients, respectively, median progression-free survival for D-VMP versus VMP was not reached (NR) versus 20.7 months in Japanese patients and NR versus 14.0 months in Korean patients. The overall response rate for D-VMP versus VMP was 96% versus 92% in Japanese patients and 91% versus 61% in Korean patients. Using next-generation sequencing, minimal residual disease negativity at 10

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsAsia, EasternBortezomibDisease-Free SurvivalFemaleHumansMaleMelphalanMiddle AgedMultiple MyelomaPrednisoloneSurvival RateAntibodies, MonoclonalBortezomibdaratumumabMelphalanPrednisoloneDaratumumabMultiple myelomaTransplant-ineligibleVMP

Identifiers

PMID31620815
PMCPMC6900260
OpenAlexW2981132455

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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.