Evidence map›Paper›PMID 36199534›Full record

ArticleChinese journal of cancer research = Chung-kuo yen cheng yen chiu2022

Clinical review considerations of class I PI3K inhibitors in hematolymphatic malignancies by Center for Drug Evaluation.

Limin Zou, Yueli Qi, Ling Tang, Yu Du, Meiyi Xiang, Xiaoming Chen, Jun Ma, Zhimin Yang

Open access · diamondAbstract read
In one paragraph

Article in Chinese journal of cancer research = Chung-kuo yen cheng yen chiu, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

8 authors at 1 institution in 1 country.

Limin ZouOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Yueli QiOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Ling TangOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Yu DuOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Meiyi XiangOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Xiaoming ChenOffice of Management and Communication, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
Jun MaHarbin Institute of Hematology and Oncology, Harbin 150010, China.
Zhimin YangOffice of Clinical Evaluation 1, Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.
National Medical Products Administration · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several phosphoinositide 3-kinase (PI3K) inhibitors are currently approved to treat hematolymphatic malignant diseases worldwide, and many drugs that have the same target are in the clinical research stage. In March 2022, duvelisib became the first PI3K inhibitor approved in China indicated for the treatment of hematolymphatic malignant diseases. Meanwhile, linperlisib and copanlisib have almost completed the technical review of the clinical specialty. The Center for Drug Evaluation (CDE) of the China National Medical Products Administration (NMPA) found that class I PI3K inhibitors can cause various degrees of immune-related adverse events, which are associated with action mechanisms, affecting the benefit-risk assessment of the drugs. On April 21, 2021, the United States Food and Drug Administration (FDA) convened the Oncologic Drugs Advisory Committee (ODAC) meeting to discuss the safety of PI3K inhibitors indicated for hematolymphatic malignancies and their related risk of death. The hematological tumor group of CDE of the China NMPA summarized and combined the data on PI3K inhibitors listed or under technical review for marketing authorization applications and found that such products may have unique efficacy and safety characteristics in Chinese patients with malignant lymphoma.

Indexed as

Class I PI3K inhibitorsefficacyhematolymphatic malignanciessafety

Identifiers

PMID36199534
PMCPMC9468018
OpenAlexW4295102659

What OpenQuestion holds

Textmetadata
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.