Evidence map›Paper›PMID 24617454›Full record

Trial reportBritish journal of haematology2014

A multicentre phase II study of vorinostat in patients with relapsed or refractory indolent B-cell non-Hodgkin lymphoma and mantle cell lymphoma.

Michinori Ogura, Kiyoshi Ando, Tatsuya Suzuki, Kenichi Ishizawa, Sung Yong Oh, Kuniaki Itoh, Kazuhito Yamamoto, Wing Yan Au, Hwei-Fang Tien, Yoshihiro Matsuno and 7 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in British journal of haematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00875056 (A Phase II Study of MK-0683 in Patients With Relapsed / Refractory Follicular Lymphoma), which is not on this map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
7.4field-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.

NCT00875056 phase2completednot on this map

A Phase II Study of MK-0683 in Patients With Relapsed / Refractory Follicular Lymphoma (FL), Other Indolent B-cell Non-Hodgkin's Lymphoma (B-NHL) or Mantle Cell Lymphoma (MCL)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2009 to 2019Enrolled56ConditionsLymphomaArmsVorinostat
3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  5. [Research progress on protein lactylation modification in malignant tumors].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2026
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  18. Advances in the multi-omics landscape of follicular lymphoma.International journal of biological sciences · 2023
    Review
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4 more citing papers are in PubMed but not listed here.

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

17 authors at 11 institutions in 4 countries.

Michinori OguraDepartment of Haematology and Oncology, Nagoya Daini Red Cross Hospital, Nagoya, Japan.
Kiyoshi Ando
Tatsuya Suzuki
Kenichi Ishizawa
Sung Yong Oh
Kuniaki Itoh
Kazuhito Yamamoto
Wing Yan Au
Hwei-Fang Tien
Yoshihiro Matsuno
Takashi Terauchi
Keiko Yamamoto
Masahiko Mori
Yoshinobu Tanaka
Takashi Shimamoto
Kensei Tobinai
Won Seog Kim
MSD K.K. (Japan) · JPNational Cancer Centre Japan · JPJapanese Red Cross Nagoya Daini Hospital · JPAichi Cancer Center · JPDong-A University · KRHokkaido University Hospital · JPNational Taiwan University Hospital · TWQueen Mary Hospital · CNSungkyunkwan University · KRTohoku University · JPTokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although initial rituximab-containing chemotherapies achieve high response rates, indolent B-cell non-Hodgkin lymphoma (B-NHL), such as follicular lymphoma (FL), is still incurable. Therefore, new effective agents with novel mechanisms are anticipated. In this multicentre phase II study, patients with relapsed/refractory indolent B-NHL and mantle cell lymphoma (MCL) received vorinostat 200 mg twice daily for 14 consecutive days in a 21-d cycle until disease progression or unacceptable toxicity occurred. The primary endpoint was overall response rate (ORR) in FL patients and safety and tolerability in all patients. Secondary endpoints included progression-free survival (PFS). Fifty-six eligible patients were enrolled; 50 patients (39 with FL, seven with other B-NHL, and four with MCL) were evaluable for ORR, and 40 patients had received rituximab-containing prior chemotherapeutic regimens. For the 39 patients with FL, the ORR was 49% [95% confidence interval (CI): 32·4, 65·2] and the median PFS was 20 months (95% CI: 11·2, 29·7). Major toxicities were manageable grade 3/4 thrombocytopenia and neutropenia. Vorinostat offers sustained antitumour activity in patients with relapsed or refractory FL with an acceptable safety profile. Further investigation of vorinostat for clinical efficacy is warranted.

Indexed as

AdultAgedAntineoplastic AgentsCombined Modality TherapyCREB-Binding ProteinDNA Mutational AnalysisE1A-Associated p300 ProteinHumansHydroxamic AcidsLymphoma, B-CellLymphoma, Mantle-CellMiddle AgedMutationNeoplasm GradingRecurrenceTreatment OutcomeAntineoplastic AgentsCREB-Binding ProteinE1A-Associated p300 ProteinHydroxamic AcidsVorinostatfollicular lymphomaHAT mutationindolent B-cell non-Hodgkin lymphomaphase II trialvorinostat

Identifiers

PMID24617454
PMCPMC4282031
OpenAlexW2004380969

What OpenQuestion holds

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Registered trials

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.