Evidence map›Paper›PMID 30360024›Full record

ArticleThe Korean journal of internal medicine2019

Modified dose of melphalan-prednisone in multiple myeloma patients receiving bortezomib plus melphalan-prednisone treatment.

Se Ryeon Lee, Hojoon Choi, Byung Hyun Lee, Ka-Won Kang, Eun Sang Yu, Dae Sik Kim, Yong Park, Chul Won Choi, Byung Soo Kim, Hwa Jung Sung

Open access · goldAbstract readComparative StudyMulticenter Study
In one paragraph

Article in The Korean journal of internal medicine, 2019. 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
0.2field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

10 authors at 1 institution in 1 country.

Se Ryeon LeeDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hojoon ChoiDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Byung Hyun LeeDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Ka-Won KangDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Eun Sang YuDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Dae Sik KimDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Yong ParkDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Chul Won ChoiDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Byung Soo KimDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hwa Jung SungDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Korea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsBortezomib plus melphalan-prednisone (VMP) is a standard treatment for multiple myeloma, particularly for patients who are ineligible for high-dose therapy. However, early discontinuation or treatment modification is often needed owing to adverse events. The aim of this study was to investigate the clinical outcomes of modifying the dose of melphalan-prednisone (MP) in patients receiving VMP.

methodsWe examined 67 patients who received a modified dose of MP, and 38 patients who received the regularly planned dose of MP. We then analyzed clinical differences between the groups.

resultsAlthough there was no difference in the proportion of discontinuation due to adverse events between dose groups, more patients in the planned-dose group experienced earlier discontinuation in general. The overall response rate (ORR) was 81.0% and complete response (CR) rate was 30.5%. After a median 15.7 months of follow-up, the median progression-free survival (PFS) and overall survival (OS) were 25.0 and 47.8 months, respectively. There was no significant difference in the ORR, CR, PFS, and OS of the two dose groups. A median of four cycles were delivered, and the median cumulative bortezomib dose was 41.6 mg/m2 . The median PFS in patients with doses ≥ 41.6 mg/m2 was longer than that in patients with doses < 41.6 mg/m2 (35.1 months vs. 9.6 months). However, when MP was < 50% of the planned dose, PFS and OS were poor.

conclusionModifying the dose of MP might be a feasible and effective therapeutic approach for multiple myeloma patients receiving VMP treatment.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBortezomibDisease ProgressionFemaleHumansMaleMelphalanMiddle AgedMultiple MyelomaPrednisoneProgression-Free SurvivalRepublic of KoreaRetrospective StudiesRisk FactorsBortezomibMelphalanPrednisoneBortezomibMelphalanModifiedMultiple myelomaPrednisone

Identifiers

PMID30360024
PMCPMC6823557
OpenAlexW2898314827

What OpenQuestion holds

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Registered trials

None linked

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.