Evidence map›Paper›PMID 27187687›Full record

ArticleBritish journal of cancer2016

A nomogram for predicting complications in patients with solid tumours and seemingly stable febrile neutropenia.

Paula Jiménez Fonseca, Alberto Carmona-Bayonas, Ignacio Matos García, Rosana Marcos, Eduardo Castañón, Maite Antonio, Carme Font, Mercè Biosca, Ana Blasco, Rebeca Lozano and 23 more

Abstract readValidation Study
In one paragraph

Article in British journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Common misconceptions in the prognostic evaluation of clinically stable patients with febrile neutropenia and solid tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Article
  6. SEOM clinical practice guideline: management and prevention of febrile neutropenia in adults with solid tumors (2018).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Article
  7. Top ten errors of statistical analysis in observational studies for cancer research.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Review
  8. Key points to optimizing management and research on cancer-associated thrombosis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Review
  9. The time has come for new models in febrile neutropenia: a practical demonstration of the inadequacy of the MASCC score.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    Article
  10. Performance of the clinical index of stable febrile neutropenia (CISNE) in different types of infections and tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    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

33 authors.

Paula Jiménez FonsecaMedical Oncology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
Alberto Carmona-BayonasHematology and Medical Oncology Department, Hospital Universitario Morales Meseguer, Calle Marqués de los Vélez s/n, Murcia 30008, Spain.
Ignacio Matos GarcíaMedical Oncology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Rosana MarcosMedical Oncology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Eduardo CastañónMedical Oncology Department, Clínica Universidad de Navarra, Pamplona, Spain.
Maite AntonioMedical Oncology Department, ICO Duran i Reynals, Barcelona, Spain.
Carme FontMedical Oncology Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Mercè BioscaMedical Oncology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Ana BlascoMedical Oncology Department, Hospital General Universitario de Valencia, Valencia, Spain.
Rebeca LozanoMedical Oncology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Avinash RamchandaniMedical Oncology Department, Hospital Universitario Insular de Gran Canaria, Las Palmas, Spain.
Carmen BeatoMedical Oncology Department, Hospital NISA Aljarafe, Sevilla, Spain.
Eva Martínez de CastroMedical Oncology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Javier EspinosaMedical Oncology Department, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain.
Jerónimo Martínez-GarcíaMedical Oncology Department, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.
Ismael GhanemMedical Oncology Department, Hospital Universitario La Paz, Madrid, Spain.
Jorge Hernando CuberoMedical Oncology Department, Hospital Universitario Miguel Servet, Zaragoza, Spain.
Isabel Aragón ManriqueMedical Oncology Department, Hospital Juan Ramón Jiménez, Huelva, Spain.
Francisco García NavalónMedical Oncology Department, Hospital General Universitario de Valencia, Valencia, Spain.
Elena SevillanoMedical Oncology Department, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
Aránzazu ManzanoMedical Oncology Department, Hospital Universitario Clínico San Carlos, Madrid, Spain.
Juan VirizuelaMedical Oncology Department, Hospital Universitario Virgen de Macarena, Sevilla, Spain.
Marcelo GarridoMedical Oncology Department, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile.
Rebeca MondéjarMedical Oncology Department, Hospital Universitario de La Princesa, Madrid, Spain.
María Ángeles ArcusaMedical Oncology Department, Consorci Sanitari de Terrassa, Barcelona, Spain.
Yaiza BonillaIntensive Care Unit, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Quionia PérezMedical Oncology Department, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.
Elena GallardoMedical Oncology Department, Complejo Universitario de Pontevedra, Pontevedra, Spain.
Maria Del Carmen SorianoMedical Oncology Department, Hospital Virgen de la Luz de Cuenca, Madrid, Spain.
Mercè CardonaInternal Medicine Department, Hospital de Tortosa Verge de la Cinta, Tarragona, Spain.
Fernando Sánchez LasherasDepartment of Construction and Manufacturing Engineering, University of Oviedo, Spain.
Juan Jesús CruzMedical Oncology Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Francisco AyalaHematology and Medical Oncology Department, Hospital Universitario Morales Meseguer, Calle Marqués de los Vélez s/n, Murcia 30008, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe sought to develop and externally validate a nomogram and web-based calculator to individually predict the development of serious complications in seemingly stable adult patients with solid tumours and episodes of febrile neutropenia (FN). PATIENTS AND

methodsThe data from the FINITE study (n=1133) and University of Salamanca Hospital (USH) FN registry (n=296) were used to develop and validate this tool. The main eligibility criterion was the presence of apparent clinical stability, defined as events without acute organ dysfunction, abnormal vital signs, or major infections. Discriminatory ability was measured as the concordance index and stratification into risk groups.

resultsThe rate of infection-related complications in the FINITE and USH series was 13.4% and 18.6%, respectively. The nomogram used the following covariates: Eastern Cooperative Group (ECOG) Performance Status ⩾2, chronic obstructive pulmonary disease, chronic cardiovascular disease, mucositis of grade ⩾2 (National Cancer Institute Common Toxicity Criteria), monocytes <200/mm(3), and stress-induced hyperglycaemia. The nomogram predictions appeared to be well calibrated in both data sets (Hosmer-Lemeshow test, P>0.1). The concordance index was 0.855 and 0.831 in each series. Risk group stratification revealed a significant distinction in the proportion of complications. With a ⩾116-point cutoff, the nomogram yielded the following prognostic indices in the USH registry validation series: 66% sensitivity, 83% specificity, 3.88 positive likelihood ratio, 48% positive predictive value, and 91% negative predictive value.

conclusionsWe have developed and externally validated a nomogram and web calculator to predict serious complications that can potentially impact decision-making in patients with seemingly stable FN.

Indexed as

NomogramsAdultCardiovascular DiseasesComorbidityFebrile NeutropeniaFemaleHumansHyperglycemiaInfectionsLikelihood FunctionsMaleMiddle AgedMucositisMulticenter Studies as TopicNeoplasmsPredictive Value of Tests

Identifiers

PMID27187687
PMCPMC4891503

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