Evidence map›Paper›PMID 23978945›Full record

Trial reportAnnals of hematology2013

CHO(E)P-14 followed by alemtuzumab consolidation in untreated peripheral T cell lymphomas: final analysis of a prospective phase II trial.

C Binder, M Ziepert, M Pfreundschuh, U Dührsen, H Eimermacher, A Aldaoud, A Rosenwald, M Loeffler, N Schmitz, L Truemper and 1 more

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

Trial report in Annals of hematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Enteropathy-Associated T cell Lymphoma.Current hematologic malignancy reports · 2021
    Review
  7. Review
  8. Article
  9. T-cell lymphomas, a challenging disease: types, treatments, and future.International journal of clinical oncology · 2017
    Review
  10. Review
  11. Therapeutic options in peripheral T cell lymphoma.Journal of hematology & oncology · 2016
    Review
  12. Review
  13. New antibody approaches to lymphoma therapy.Journal of hematology & oncology · 2014
    Review
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 5 institutions in 1 country.

C BinderDepartment of Haematology and Oncology, Göttingen Comprehensive Cancer Center (G-CCC), Georg-August-University, 37099, Goettingen, Germany.
M Ziepert
M Pfreundschuh
U Dührsen
H Eimermacher
A Aldaoud
A Rosenwald
M Loeffler
N Schmitz
L Truemper
German High Grade Non-Hodgkin’s Lymphoma Study Group (DSHNHL)
University of Göttingen · DEAsklepios Klinik St. Georg · DESaarland University · DEUniversity of Würzburg · DEKatholisches Krankenhaus St. Johann Nepomuk · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rate of long-term remissions after treatment of peripheral T cell lymphomas (PTCL) with standard CHOP-like protocols is unsatisfactory. A prospective multicenter phase II trial was initiated in untreated patients with PTCL of all International Prognostic Index-risk groups, evaluating alemtuzumab consolidation in patients with complete or good partial remission after CHO(E)P-14 induction. Twenty-nine (70.7 %) of the 41 enrolled patients received alemtuzumab consolidation (133 mg in total). The main grades 3-4 toxicities during alemtuzumab therapy were infections and neutropenia with one potentially treatment-related death. Complete responses were seen in 58.5 %, partial responses in 2.4 % and 29.3 % had progressive disease. After a median observation time of 46 months, 19 patients have died, 16 of them due to lymphoma and/or salvage therapy complications. Event-free and overall survival at 3 years in the whole intent to treat population are 32.3 and 62.5 %, respectively, and 42.4 and 75.1 % in the patients who received alemtuzumab. In conclusion, application of a short course of alemtuzumab after CHO(E)P-14 induction is feasible although complicated by severe infections. A current phase III trial, applying alemtuzumab as part of the initial chemotherapy protocol to avoid early progression, will further clarify its significance for the therapeutic outcome.

Indexed as

AdultAgedAlemtuzumabAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesCyclophosphamideDisease ProgressionDoxorubicinDrug Administration ScheduleFemaleFollow-Up StudiesHumansLymphoma, T-Cell, PeripheralMaleAlemtuzumabAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCyclophosphamideDoxorubicinPrednisoneVincristine

Identifiers

PMID23978945
PMCPMC3790248
OpenAlexW1971253196

What OpenQuestion holds

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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.