Evidence map›Paper›PMID 29703335›Full record

Trial reportThe Lancet. Haematology2018

CHOP versus GEM-P in previously untreated patients with peripheral T-cell lymphoma (CHEMO-T): a phase 2, multicentre, randomised, open-label trial.

Mary Gleeson, Clare Peckitt, Ye Mong To, Laurice Edwards, Jacqueline Oates, Andrew Wotherspoon, Ayoma D Attygalle, Imene Zerizer, Bhupinder Sharma, Sue Chua and 18 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Lancet. Haematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
7.5field-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.

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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Review
  8. Article
  9. Failing Forward in Peripheral T-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Long-time follow-up of patients with untreated peripheral T cell lymphoma following chidamide combined with cyclophosphamide, epirubicin, vindesine, prednisone, and etoposide therapy: a single-center propensity score-matching study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. How to Sequence Therapies in Peripheral T Cell Lymphoma.Current treatment options in oncology · 2021
    Review
  20. 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

28 authors at 16 institutions in 2 countries.

Mary GleesonThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Clare PeckittThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Ye Mong ToThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Laurice EdwardsThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Jacqueline OatesThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Andrew WotherspoonThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Ayoma D AttygalleThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Imene ZerizerThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Bhupinder SharmaThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Sue ChuaThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Ruwaida BegumThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Ian ChauThe Royal Marsden NHS Foundation Trust, London and Surrey, UK.
Peter JohnsonCancer Research UK Centre, University of Southampton, Southampton, UK.
Kirit M ArdeshnaUniversity College Hospital London, London, UK.
Eliza A HawkesOlivia Newton John Cancer Research Institute, Austin Health, Melbourne, VA, Australia; Eastern Health, Melbourne, VA, Australia.
Marian P MachetaBlackpool Teaching Hospitals, Blackpool, UK.
Graham P CollinsOxford Cancer and Haematology Centre, Churchill Hospital, Oxford, UK.
John RadfordUniversity of Manchester and the Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Adam ForbesRoyal Cornwall Hospital, Truro, UK.
Alistair HartNew Victoria Hospital, Glasgow, UK.
Silvia MontotoSt Bartholomew's Hospital, London, UK.
Pamela McKayBeatson West of Scotland Cancer Centre, Glasgow, UK.
Kim BensteadGloucestershire Hospitals NHS Foundation Trust, Gloucestershire, UK.
Nicholas MorleySheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Nagesh KalakondaUniversity of Liverpool, Liverpool, UK.
Yasmin HasanSandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK.
Deborah TurnerTorbay and South Devon NHS Trust, Torquay, UK.
David CunninghamThe Royal Marsden NHS Foundation Trust, London and Surrey, UK. Electronic address: david.cunningham@rmh.nhs.uk.
Royal Marsden NHS Foundation Trust · GBBeatson West of Scotland Cancer Centre · GBBlackpool Teaching Hospitals NHS Foundation Trust · GBCancer Research UK · GBChurchill Hospital · GBGloucestershire Hospitals NHS Foundation Trust · GBManchester Academic Health Science Centre · GBNew Victoria Hospital · GBOlivia Newton-John Cancer Wellness & Research Centre · AURoyal Cornwall Hospital · GBSandwell & West Birmingham Hospitals NHS Trust · GBSheffield Teaching Hospitals NHS Foundation Trust · GBSt Bartholomew's Hospital · GBTorbay and South Devon NHS Foundation Trust · GBUniversity College Hospital · GBUniversity of Liverpool · GB

Funding

Cancer Research UK 13319
6 · The paper itself

Abstract

backgroundOutcomes with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) or CHOP-like chemotherapy in peripheral T-cell lymphoma are poor. We investigated whether the regimen of gemcitabine, cisplatin, and methylprednisolone (GEM-P) was superior to CHOP as front-line therapy in previously untreated patients.

methodsWe did a phase 2, parallel-group, multicentre, open-label randomised trial in 47 hospitals: 46 in the UK and one in Australia. Participants were patients aged 18 years and older with bulky (tumour mass diameter >10 cm) stage I to stage IV disease (WHO performance status 0-3), previously untreated peripheral T-cell lymphoma not otherwise specified, angioimmunoblastic T-cell lymphoma, anaplastic lymphoma kinase-negative anaplastic large cell lymphoma, enteropathy-associated T-cell lymphoma, or hepatosplenic γδ T-cell lymphoma. We randomly assigned patients (1:1) stratified by subtype of peripheral T-cell lymphoma and international prognostic index to either CHOP (intravenous cyclophosphamide 750 mg/m

findingsBetween June 18, 2012, and Nov 16, 2016, we randomly assigned 87 patients to treatment, 43 to CHOP and 44 to GEM-P. A planned unmasked review of efficacy data by the independent data monitoring committee in November, 2016, showed that the number of patients with a confirmed or unconfirmed complete response with GEM-P was non-significantly inferior compared with CHOP and the trial was closed early. At a median follow-up of 27·4 months (IQR 16·6-38·4), 23 patients (62%) of 37 assessable patients assigned to CHOP had achieved a complete response or unconfirmed complete response compared with 17 (46%) of 37 assigned to GEM-P (odds ratio 0·52, 95% CI 0·21-1·31; p=0·164). The most common adverse events of grade 3 or worse in both groups were neutropenia (17 [40%] with CHOP and nine [20%] with GEM-P), thrombocytopenia (4 [10%] with CHOP and 13 [30%] with GEM-P, and febrile neutropenia (12 [29%] with CHOP and 3 [7%] with GEM-P). Two patients (5%) died during the study, both in the GEM-P group, from lung infections.

interpretationThe number of patients with a complete response or unconfirmed complete response did not differ between the groups, indicating that GEM-P was not superior for this outcome. CHOP should therefore remain the reference regimen for previously untreated peripheral T-cell lymphoma.

fundingBloodwise and the UK National Institute of Health Research.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCisplatinCyclophosphamideDeoxycytidineDoxorubicinFemaleGemcitabineHumansLymphoma, T-Cell, PeripheralMaleMethylprednisoloneMiddle AgedPrednisoneVincristineCisplatinCyclophosphamideDeoxycytidineDoxorubicinGemcitabineMethylprednisolonePrednisoneVincristine

Identifiers

PMID29703335
PMCPMC5946805
OpenAlexW2801119848

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.