Evidence map›Paper›PMID 35353920›Full record

ArticleJournal of clinical laboratory analysis2022

Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real-world analysis.

Yu-Tong Wang, Li Bao, Bin Chu, Xiao-Huan Chen, Min-Qiu Lu, Lei Shi, Shan Gao, Li-Juan Fang, Qiu-Qing Xiang, Yue-Hua Ding

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. The numerous facets of 1q21Oncology letters · 2024
    Review
  5. Article
  6. Article
  7. 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

10 authors at 1 institution in 1 country.

Yu-Tong WangDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Li BaoDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.ORCID https://orcid.org/0000-0002-6436-1492
Bin ChuDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Xiao-Huan ChenDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Min-Qiu LuDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Lei ShiDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Shan GaoDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Li-Juan FangDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Qiu-Qing XiangDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Yue-Hua DingDepartment of Hematology, Beijing Jishuitan Hospital, 4th Clinical Medical College of Peking University, Beijing, China.
Peking University · CN

Funding

Beijing JST Research Funding QN-201908Beijing JST Research Funding ZR-201909Beijing Municipal Excellent Talents Foundation 2018000021469G223
6 · The paper itself

Abstract

introductionThe gain/amplification (amp) of 1q21 is one of the most common high-risk chromosome abnormality (HRCA) in multiple myeloma (MM). The prognostic value of 1q21+ remains to be controversial on the status of gain or amp and the combination of other HRCAs.

methodsIn this retrospective study, we included 318 newly diagnosed MM (NDMM) patients who had fluorescence in situ hybridization (FISH) data and treated with novel agents in our department.

resultsOur study noted MM patients with amp 1q21 were more likely accompanied with t(4;14), t(14;16), and t(14;20). Patients with amp 1q21 presented with elder age, advanced Revised International Staging System (R-ISS) stages, anemia, and more plasma cells in bone marrow compared to patients with gain 1q21 alone and no 1q21+. Moreover, amp 1q21 alone correlated with shorter progression-free survival (PFS) (22.8m vs. 40.5m vs. 39.6m) and overall survival (OS) (45.2m vs. NA vs. 83.5m) compared with gain 1q21 alone and no FISH abnormalities. Although the high ratio of proteasome inhibitor and immunomodulatory drugs used in patients with amp 1q21, the overall response (ORR) was the lowest compared with no 1q21+ and gain 1q21. Multivariate analysis defined amp 1q21 as an independent prognostic marker for NDMM patients, rather than gain 1q21.

conclusionThe amp 1q21 predict inferior treatment response and survival, especially coexisted with high-risk IgH translocation.

Indexed as

Multiple MyelomaChromosome AberrationsHumansIn Situ Hybridization, FluorescencePrognosisRetrospective StudiesAmp 1q21FISHhigh-risk cytogenetic abnormalitymultiple myeloma

Identifiers

PMID35353920
PMCPMC9280004
OpenAlexW4220914920

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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.