Evidence map›Paper›PMID 35459873›Full record

Trial reportLeukemia2022

Integrated clinical and genomic evaluation of guadecitabine (SGI-110) in peripheral T-cell lymphoma.

Jonathan Wong, Emily Gruber, Belinda Maher, Mark Waltham, Zahra Sabouri-Thompson, Ian Jong, Quinton Luong, Sidney Levy, Beena Kumar, Daniella Brasacchio and 18 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Journal for immunotherapy of cancer · 2025
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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

28 authors at 8 institutions in 1 country.

Jonathan Wong *Monash Haematology, Monash Health, Clayton, VIC, Australia.
Emily Gruber *Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0001-5990-036X
Belinda Maher *Monash Haematology, Monash Health, Clayton, VIC, Australia.
Mark WalthamBlood Cancer Therapeutics Laboratory, Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.ORCID http://orcid.org/0000-0001-9623-8133
Zahra Sabouri-ThompsonBlood Cancer Therapeutics Laboratory, Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
Ian JongMonash Health Imaging, Monash Health, Clayton, VIC, Australia.
Quinton LuongBlood Cancer Therapeutics Laboratory, Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
Sidney LevyMonash Health Imaging, Monash Health, Clayton, VIC, Australia.
Beena KumarMonash Pathology, Monash Health, Clayton, VIC, Australia.
Daniella BrasacchioBlood Cancer Therapeutics Laboratory, Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
Wendy JiaPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Joan SoPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Hugh SkinnerPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Alexander LewisPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Simon J HoggSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia.
Stephin VervoortSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia.
Carmen DiCorletoMonash Haematology, Monash Health, Clayton, VIC, Australia.
Micheleine UheMonash Haematology, Monash Health, Clayton, VIC, Australia.
Jeanette GamgeeMonash Haematology, Monash Health, Clayton, VIC, Australia.
Stephen OpatMonash Haematology, Monash Health, Clayton, VIC, Australia.ORCID http://orcid.org/0000-0002-0308-6458
Gareth P GregoryMonash Haematology, Monash Health, Clayton, VIC, Australia.
Galina PolekhinaDepartment of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-9535-9291
John ReynoldsBiostatistics Consulting Platform, Monash University and Alfred Health, Prahran, VIC, Australia.ORCID http://orcid.org/0000-0002-8825-8625
Eliza A HawkesOlivia Newton John Cancer Wellness and Research Centre, at Austin Health, Heidelberg, VIC, Australia.
Gajan KailainathanHaematology Department, Concord Repatriation General Hospital, Concord, NSW, Australia.
Robin GasiorowskiHaematology Department, Concord Repatriation General Hospital, Concord, NSW, Australia.ORCID http://orcid.org/0000-0003-1225-8757
Lev M KatsSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0001-8742-8138
Jake ShorttMonash Haematology, Monash Health, Clayton, VIC, Australia. jake.shortt@monash.edu.ORCID http://orcid.org/0000-0003-3185-6488
Monash Health · AUPeter MacCallum Cancer Centre · AUThe University of Melbourne · AUAlfred Health · AUConcord Repatriation General Hospital · AUMonash University · AUOlivia Newton-John Cancer Wellness & Research Centre · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T-cell lymphoma (PTCL) is a rare, heterogenous malignancy with dismal outcomes at relapse. Hypomethylating agents (HMA) have an emerging role in PTCL, supported by shared mutations with myelodysplasia (MDS). Response rates to azacitidine in PTCL of follicular helper cell origin are promising. Guadecitabine is a decitabine analogue with efficacy in MDS. In this phase II, single-arm trial, PTCL patients received guadecitabine on days 1-5 of 28-day cycles. Primary end points were overall response rate (ORR) and safety. Translational sub-studies included cell free plasma DNA sequencing and functional genomic screening using an epigenetically-targeted CRISPR/Cas9 library to identify response predictors. Among 20 predominantly relapsed/refractory patients, the ORR was 40% (10% complete responses). Most frequent grade 3-4 adverse events were neutropenia and thrombocytopenia. At 10 months median follow-up, median progression free survival (PFS) and overall survival (OS) were 2.9 and 10.4 months respectively. RHOA

Indexed as

AzacitidineLymphoma, T-Cell, PeripheralDecitabineGenomicsHumansMyelodysplastic SyndromesNeoplasm Recurrence, LocalNeutropeniaTreatment OutcomeAzacitidineDecitabineguadecitabine

Identifiers

PMID35459873
PMCPMC9162925
OpenAlexW4224276050

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.