Evidence map›Paper›PMID 38644985›Full record

ArticleJournal of hematology2024

Effective Management of Polycythemia Vera With Ropeginterferon Alfa-2b Treatment.

Shan Shan Suo, Rong Feng Fu, Albert Qin, Zong Hong Shao, Jie Bai, Su Ning Chen, Ming Hui Duan, Hu Zhou, Na Xu, Su Jiang Zhang and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 5 pooled it
8.8field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 5 syntheses or guidelines pooled it, 20 citations in OpenAlex.

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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

24 authors at 14 institutions in 3 countries.

Shan Shan SuoThe First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Rong Feng FuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.
Albert QinMedical Research & Clinical Operations, PharmaEssentia Corporation, Taipei, Taiwan, Republic of China.
Zong Hong ShaoThe Second Hospital of Tianjin Medical University, Tianjin, China.
Jie BaiThe Second Hospital of Tianjin Medical University, Tianjin, China.
Su Ning ChenThe First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Ming Hui DuanPeking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Hu ZhouAffiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital, Zhengzhou, Henan, China.
Na XuNanfang Hospital of Southern Medical University, Guangzhou, Guangdong, China.
Su Jiang ZhangRuijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Xue Lan ZuoZhongnan Hospital, Wuhan University, Wuhan, Hubei, China.
Xin DuShenzhen Second People's Hospital, Shenzhen, Guangdong, China.
Li WangThe First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Pei LiHuashan Hospital of Fudan University, Shanghai, China.
Xu Han ZhangThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Dao Xiang WuPharmaEssentia Biotech (Beijing) Limited, Beijing, China.
Ya Ning LiPharmaEssentia Biotech (Beijing) Limited, Beijing, China.
Jing Jing ZhangPharmaEssentia Biotech (Beijing) Limited, Beijing, China.
Wei WangPharmaEssentia Biotech (Beijing) Limited, Beijing, China.
Wei Hong ShenPharmaEssentia Biotech (Beijing) Limited, Beijing, China.
Oleh ZagrijtschukPharmaEssentia USA Corporation, Burlington, MA, USA.
Toshiaki SatoPharmaEssentia Japan K.K., Motoakasaka, Minato-ku, Tokyo, Japan.
Zhi Jian XiaoInstitute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Jie JinThe First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Sinovac Biotech · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFirst Affiliated Hospital Zhejiang University · CNTianjin Medical University · CNChongqing Medical University · CNEA Pharma (Japan) · JPFudan University · CNNanfang Hospital · CNRuijin Hospital · CNShenzhen Second People's Hospital · CNSoochow University · CNUniversity of Science and Technology of China · CNWuhan University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Polycythemia vera (PV) is a myeloproliferative neoplasm. Ropeginterferon alfa-2b is a new-generation polyethylene glycol-conjugated proline-interferon. It is approved for the treatment of PV at a starting dose of 100 µg (50 µg for patients receiving hydroxyurea (HU)) and dose titrations up to 500 µg by 50 µg increments. The study was aimed at assessing its efficacy and safety at a higher starting dose and simpler intra-patient dose escalation. Methods: Forty-nine patients with PV having HU intolerance from major hospitals in China were treated biweekly with an initial dose of 250 µg, followed by 350 µg and 500 µg thereafter if tolerated. Complete hematological response (CHR) was assessed every 12 weeks based on the European LeukemiaNet criteria. The primary endpoint was the CHR rate at week 24. The secondary endpoints included CHR rates at weeks 12, 36 and 52, changes of Results: The CHR rates were 61.2%, 69.4% and 71.4% at weeks 24, 36, and 52, respectively. Mean allele burden of the driver mutation Conclusion: The 250-350-500 µg dosing regimen was well tolerated and effectively induced CHR and MR and managed spleen size increase. Our findings demonstrate that ropeginterferon alfa-2b at this dosing regimen can provide an effective management of PV and support using this dosing regimen as a treatment option.

Indexed as

Complete hematological responseHydroxyurea resistance or intoleranceJAK2V617F allele burdenMolecular responsePolycythemia veraRopeginterferon alfa-2b

Identifiers

PMID38644985
PMCPMC11027776
OpenAlexW4394620901

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.