Evidence map›Paper›PMID 38150138›Full record

ArticleInternational journal of hematology2024

Japanese phase Ib study of the oral PI3K-δ and -γ inhibitor duvelisib in patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma.

Shinichi Makita, Shuichi Ota, Yuko Mishima, Kensuke Usuki, Daisuke Ennishi, Masamitsu Yanada, Noriko Fukuhara, Ryusuke Yamamoto, Atsushi Takamine, Go Nohara and 1 more

Abstract readMulticenter StudyClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 8 institutions in 1 country.

Shinichi MakitaDepartment of Hematology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan. smakita@ncc.go.jp.
Shuichi OtaDepartment of Hematology, Sapporo Hokuyu Hospital, Hokkaido, Japan.
Yuko MishimaDepartment of Hematology Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Kensuke UsukiDepartment of Hematology, NTT Medical Center Tokyo, Tokyo, Japan.
Daisuke EnnishiCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.
Masamitsu YanadaDepartment of Hematology and Cell Therapy, Aichi Cancer Center, Aichi, Japan.
Noriko FukuharaDepartment of Hematology, Tohoku University Hospital, Miyagi, Japan.
Ryusuke YamamotoDepartment of Hematology, Kobe City Medical Center General Hospital, Hyogo, Japan.
Atsushi TakaminePharmaceutical Research & Development Department, Yakult Honsha Co., Ltd., Tokyo, Japan.
Go NoharaPharmaceutical Research & Development Department, Yakult Honsha Co., Ltd., Tokyo, Japan.
Koji IzutsuDepartment of Hematology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Yakult Honsha (Japan) · JPAichi Cancer Center · JPJapanese Foundation For Cancer Research · JPKobe City Medical Center General Hospital · JPNTT Medical Center · JPOkayama University Hospital · JPSapporo Hokuyu Hospital · JPTohoku University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This phase Ib, open-label, single-arm, multicenter study assessed the efficacy and safety of duvelisib, an oral dual inhibitor of phosphatidylinositol 3-kinase-δ and -γ, in Japanese patients with relapsed or refractory (r/r) chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Duvelisib was administered orally at 25 mg twice a day (BID) until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR) and all responses were assessed by an independent review committee. Nine CLL patients and 1 SLL patient were enrolled. ORR was 80% (95% confidence interval 44.4, 97.5) for all 10 patients. All 6 patients previously treated with a Bruton's tyrosine kinase (BTK) or BCL2 inhibitor achieved a partial response. The most common adverse events were neutropenia (50%), diarrhea (40%), anemia, hypokalemia, constipation and rash (30% each). The most common grade ≥ 3 adverse events were neutropenia (50%), anemia (30%) and thrombocytopenia (20%). Duvelisib 25 mg BID showed favorable efficacy and a manageable safety profile in selected Japanese patients with r/r CLL/SLL, including patients previously treated with BTK or BCL2 inhibitors (Clinical trial registration: jRCTs2080224791).

Indexed as

AnemiaAntineoplastic AgentsIsoquinolinesLeukemia, Lymphocytic, Chronic, B-CellNeutropeniaPurinesHumansJapanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-bcl-2RecurrenceAntineoplastic AgentsduvelisibIsoquinolinesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-bcl-2PurinesClinical trialCLL/SLLDuvelisibJapanesePI3K

Identifiers

PMID38150138
OpenAlexW4390273649

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.