Evidence map›Paper›PMID 41052983›Full record

Trial reportBlood cancer journal2025

Randomized Phase 3 study of pomalidomide cyclophosphamide dexamethasone versus pomalidomide dexamethasone in relapse or refractory myeloma: an Asian Myeloma Network study (AMN003).

Jin Seok Kim, Yang Song, Wei-Ying Jen, C S Chim, Je-Jung Lee, Sung-Soo Yoon, Soo Chin Ng, Gin Gin Gan, Hiroshi Handa, Jae Hoon Lee and 12 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Blood cancer journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03143049 (Randomized Phase 3 Study of Pomalidomide-Cyclophosphamide-Dexamethasone), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT03143049 phase3unknown statusnot on this map

Randomized Phase 3 Study of Pomalidomide-Cyclophosphamide-Dexamethasone (PCD) Versus Pomalidomide-Dexamethasone (PD) in Relapse or Refractory Myeloma. An AMN Study

TypeinterventionalSponsorNational University Hospital, SingaporeRan2017 to 2022Enrolled120ConditionsRelapse Multiple MyelomaArmsPCD, PD
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
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

22 authors.

Jin Seok Kim *Division of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Severance Hospital, Blood Cancer Research Institute, Seoul, Republic of Korea.ORCID 0000-0001-8986-8436
Yang Song *Department of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.
Wei-Ying JenDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.
C S ChimComprehensive Oncology Centre, 3/F, Li Shu Fan Block, Hong Kong Sanatorium & Hospital, Happy Valley, Hong Kong, China.ORCID 0000-0003-2427-915X
Je-Jung LeeChonnam National University Hwasun Hospital, Hwasun, Republic of South Korea.ORCID 0000-0002-4635-5697
Sung-Soo YoonDivision of Hematology/Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0003-2591-7459
Soo Chin NgSubang Jaya Medical Center, Petaling Jaya, Malaysia.
Gin Gin GanDepartment of Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Hiroshi HandaDepartment of Hematology, Gunma University Hospital, Maebashi, Gunma, Japan.ORCID 0000-0003-3753-9862
Jae Hoon LeeGachon University Gil Medical Center, Incheon, Republic of South Korea.
Kihyun KimSungkyunkwan University School of Medicine Samsung Medical Center, Seoul, Republic of South Korea.
Shigeki ItoDepartment of Hematology & Oncology, Iwate Medical University Hospital, Yahaba, Japan.
Jeffrey Shang-Yi HuangNational Taiwan University, Taipei, Taiwan.
Chang Ki MinSeoul St. Mary's Hospital, The Catholic University of Korea, Seoul, South Korea.
Melissa Ooi Gaik MingDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.ORCID 0000-0002-7392-0655
Sanjay de MelDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.ORCID 0000-0002-8881-3537
Cinnie SoekojoDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.
Xinhua LiSingapore Clinical Research Institute, Singapore, Singapore.
Neha AwasthiSingapore Clinical Research Institute, Singapore, Singapore.
Yogesh PokharkarSingapore Clinical Research Institute, Singapore, Singapore.
Brian Gm DurieSamuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Outpatient Cancer Center, Los Angeles, CA, USA.
Wee-Joo ChngDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore. mdccwj@nus.edu.sg.ORCID 0000-0003-2578-8335

Funding

Bristol-Myers Squibb Company | Bristol-Myers Squibb Canada (BMS Canada) They provided the study drug (pomalidomide) and also some funding for conduct of the study
6 · The paper itself

Abstract

Pomalidomide has been shown to improve survival in patients with relapsed/refractory myeloma (RRMM). However, the optimal pomalidomide-based combinations in RRMM are not known. This study compared pomalidomide, cyclophosphamide, dexamethasone (PCD) with pomalidomide and dexamethasone (PD) in Asian patients with RRMM. Patients were randomly assigned to receive PCD or PD. Patients received pomalidomide at 4 mg from days 1 to 21, dexamethasone at 40 mg once a week, and those in the PCD arm received cyclophosphamide at 400 mg once weekly for three weeks. The primary endpoint was progression-free survival. One hundred and twenty-two patients were randomized (62 PCD, 60 PD). Baseline characteristics were comparable between both arms. The median prior lines of therapy were three. At a median follow-up of 13.5 (median range 9-18) months, median progression free survival was significantly longer at 10.9 months (95% confidence interval 7.1-27.7) in the PCD group compared with 5.8 months (95% CI, 4.4-6.9) in the PD group (hazard ratio 0.43; p < 0.001). Adverse events rates were similar in both arms. The most common grade ≥3 adverse events were hematological toxicities and pneumonia. 34 deaths occurred during the study (PCD: 17; PD: 17) and three were deemed to be related to study treatment. In Asian patients with RRMM after exposure to proteasome inhibitor and lenalidomide, progression-free survival was significantly prolonged with the addition of cyclophosphamide to PD, with a manageable safety profile.Trial ID: Registered at www.clinicaltrials.gov : NCT03143049.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDexamethasoneMultiple MyelomaThalidomideAdultAgedAged, 80 and overCyclophosphamideFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalCyclophosphamideDexamethasonepomalidomideThalidomide

Identifiers

PMID41052983
PMCPMC12501207

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Registered trials

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.