Evidence map›Paper›PMID 35717027›Full record

ArticleJournal for immunotherapy of cancer2022

Phase 1, dose-escalation study of guadecitabine (SGI-110) in combination with pembrolizumab in patients with solid tumors.

Dionysis Papadatos-Pastos, Wei Yuan, Abhijit Pal, Mateus Crespo, Ana Ferreira, Bora Gurel, Toby Prout, Malaka Ameratunga, Maxime Chénard-Poirier, Andra Curcean and 21 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02998567 (HyPeR), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.3field-weighted citation impact, top 3% 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.

NCT02998567 phase1active not recruitingnot on this map

HyPeR: A Phase 1, Dose Escalation Study of Guadecitabine /ASTX727 in Combination With Pembrolizumab (MK3475) in Patients With Refractory Solid Tumours

TypeinterventionalSponsorRoyal Marsden NHS Foundation TrustRan2017 to 2026Enrolled60ConditionsNon Small Cell Lung CancerArmsGuadecitabine, Pembrolizumab, ASTX727
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 53 citations in OpenAlex.

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  18. Regulation and application of mScience China. Life sciences · 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

31 authors at 3 institutions in 1 country.

Dionysis Papadatos-Pastos *Clinical Research Facility, University College London Hospitals, London, UK.
Wei Yuan *Cancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Abhijit PalDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Mateus CrespoCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Ana FerreiraCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Bora GurelCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Toby ProutDrug Development Unit - Investigator Initiated Trials Team, Institute of Cancer Research, Sutton, UK.
Malaka AmeratungaDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Maxime Chénard-PoirierDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Andra CurceanDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Claudia BertanCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Chloe BakerCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Susana MirandaCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Nahal MasrourDepartment of Surgery and Cancer, Imperial College London, London, UK.
Wentin ChenDepartment of Surgery and Cancer, Imperial College London, London, UK.
Rita PereiraCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Ines FigueiredoCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Ricardo MorillaDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Ben JenkinsClinical Trials and Statistics Unit, Institute of Cancer Research, Sutton, UK.
Anna ZachariouDrug Development Unit - Investigator Initiated Trials Team, Institute of Cancer Research, Sutton, UK.
Ruth RiisnaesCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Mona ParmarDrug Development Unit - Investigator Initiated Trials Team, Institute of Cancer Research, Sutton, UK.
Alison TurnerDrug Development Unit - Investigator Initiated Trials Team, Institute of Cancer Research, Sutton, UK.
Suzanne CarreiraCancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.ORCID 0000-0002-5077-5379
Christina YapClinical Trials and Statistics Unit, Institute of Cancer Research, Sutton, UK.ORCID 0000-0002-6715-2514
Robert BrownDepartment of Surgery and Cancer, Imperial College London, London, UK.
Nina TunariuDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Udai BanerjiDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Juanita LopezDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Johann de Bono *Cancer Biomarkers Team, Institute of Cancer Research, Sutton, UK.
Anna Minchom *Drug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK anna.minchom@icr.ac.uk.ORCID 0000-0002-9339-7101
Institute of Cancer Research · GBImperial College London · GBUniversity College London Hospitals NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData suggest that immunomodulation induced by DNA hypomethylating agents can sensitize tumors to immune checkpoint inhibitors. We conducted a phase 1 dose-escalation trial (NCT02998567) of guadecitabine and pembrolizumab in patients with advanced solid tumors. We hypothesized that guadecitabine will overcome pembrolizumab resistance.

methodsPatients received guadecitabine (45 mg/m

resultsBetween January 2017 and January 2020, 34 patients were enrolled. The recommended phase II dose was guadecitabine 30 mg/m

conclusionsGuadecitabine in combination with pembrolizumab is tolerable with biological and anticancer activity. Reversal of previous resistance to immune checkpoint inhibitors is demonstrated.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsNeoplasmsAntibodies, Monoclonal, HumanizedAzacitidineHumansImmune Checkpoint InhibitorsAntibodies, Monoclonal, HumanizedAzacitidineguadecitabineImmune Checkpoint Inhibitorspembrolizumabdrug therapy, combinationguadecitabinemethylationpembrolizumab

Identifiers

PMID35717027
PMCPMC9240883
OpenAlexW4283124134

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.