Evidence map›Paper›PMID 27226433›Full record

Trial reportBlood2016

Complex karyotypes and KRAS and POT1 mutations impact outcome in CLL after chlorambucil-based chemotherapy or chemoimmunotherapy.

Carmen Diana Herling, Marion Klaumünzer, Cristiano Krings Rocha, Janine Altmüller, Holger Thiele, Jasmin Bahlo, Sandra Kluth, Giuliano Crispatzu, Marco Herling, Joanna Schiller and 10 more

Registry-linked trialAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04059081 (A Prospective Cohort of Obinutuzumab and Chlorambucil), which is not on this map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
11.5field-weighted citation impact, top 1% 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.

NCT04059081 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

A Prospective Cohort of Obinutuzumab and Chlorambucil (GC) Chemotherapy for the Treatment of Elderly Patients With Chronic Lymphocytic Leukemia Including Next- Generation Sequencing (NGS)-Based Assessment

TypeinterventionalSponsorDeok-Hwan YangRan2019 to 2022Enrolled31ConditionsChronic Lymphocytic LeukemiaArmsObinutuzumab
3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Guideline
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  3. Trial
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  5. Article
  6. Article
  7. Review
  8. Chromoanagenesis Detection in Chronic Lymphocytic Leukemia.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  11. Article
  12. Review
  13. Article
  14. Cancers · 2022
    Article
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  16. Review
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  20. Review

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 2 countries.

Carmen Diana HerlingDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Marion KlaumünzerDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Cristiano Krings RochaDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Janine AltmüllerCologne Center for Genomics, and.
Holger ThieleCologne Center for Genomics, and.
Jasmin BahloDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Sandra KluthDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Giuliano CrispatzuDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn, Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Cologne, Germany;
Marco HerlingDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn, Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Cologne, Germany;
Joanna SchillerDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Anja EngelkeDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Eugen TauschDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany; and.
Hartmut DöhnerDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany; and.
Kirsten FischerDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Valentin GoedeDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Peter NürnbergCologne Center for Genomics, and Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Cologne, Germany; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
Hans Christian ReinhardtDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn, Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Cologne, Germany;
Stephan StilgenbauerDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany; and.
Michael HallekDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn, Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Cologne, Germany;
Karl-Anton KreuzerDepartment of Internal Medicine I, Center of Integrated Oncology Cologne-Bonn.
Integrated Oncology (United States) · USCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEUniversity Hospital Ulm · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic instability is a feature of chronic lymphocytic leukemia (CLL) with adverse prognosis. We hypothesized that chromosomal translocations or complex karyotypes and distinct somatic mutations may impact outcome after first-line chemoimmunotherapy of CLL patients. We performed metaphase karyotyping and next-generation sequencing (NGS) of 85 genes in pretreatment blood samples obtained from 161 patients registered for CLL11, a 3-arm phase 3 trial comparing frontline chlorambucil (Clb) vs Clb plus rituximab (Clb-R) or Clb plus obinutuzumab in CLL patients with significant comorbidity. Chromosomal aberrations as assessed by karyotyping were observed in 68.8% of 154 patients, 31.2% carried translocations, and 19.5% showed complex karyotypes. NGS revealed 198 missense/nonsense mutations and 76 small indels in 76.4% of patients. The most frequently mutated genes were NOTCH1, SF3B1, ATM, TP53, BIRC3, POT1, XPO1, and KRAS Sole chemotherapy, treatment with Clb-R, or genetic lesions in TP53 (9.9% of patients) and KRAS (6.2% of patients) were significantly associated with nonresponse to study therapy. In multivariate models, complex karyotypes and POT1 mutations (8.1% of patients) represented significant prognostic factors for an unfavorable survival, independently of IGHV mutation status, Binet stage, and serum β-2-microglobuline. Patients with the copresence of complex karyotypes and deletions/mutations involving TP53 demonstrated a particularly short survival. In summary, this is the first prospective, controlled study in CLL patients that shows a role of complex karyotype aberrations as an independent prognostic factor for survival after front-line therapy. Moreover, the study identifies mutations in KRAS and POT1 as novel determinants of outcome after chemoimmunotherapy using chlorambucil and anti-CD20 treatment.

Indexed as

Abnormal KaryotypeLeukemia, Lymphocytic, Chronic, B-CellAgedAged, 80 and overChlorambucilFemaleHumansMaleMiddle AgedProto-Oncogene Proteins p21(ras)RituximabShelterin ComplexTelomere-Binding ProteinsChlorambucilKRAS protein, humanPOT1 protein, humanProto-Oncogene Proteins p21(ras)RituximabShelterin ComplexTelomere-Binding Proteins

Identifiers

PMID27226433
OpenAlexW2407857284

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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.