Evidence map›Paper›PMID 34417960›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2022

Post-hematopoietic stem cell transplant squamous cell carcinoma in patients with Fanconi anemia: a dreadful enemy.

L Murillo-Sanjuán, J Balmaña, A de Pablo García-Cuenca, J Lorente Guerrero, M L Uria Oficialdegui, E Carrasco, C Diaz-de-Heredia

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 41% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Article
  7. Importance of Population-Based Cancer Risk Information in the Care of Patients With Rare Genetic Disorders.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    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

7 authors at 1 institution in 1 country.

L Murillo-SanjuánDepartment of Pediatric Oncology and Hematology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0001-6925-260X
J BalmañaDepartment of Medical Oncology and Hereditary Cancer Genetics Group, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
A de Pablo García-CuencaDepartment of Oral and Maxillofacial Surgery, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
J Lorente GuerreroDepartment of Otorhinolaryngology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
M L Uria OficialdeguiDepartment of Pediatric Oncology and Hematology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
E CarrascoDepartment of Medical Oncology and Hereditary Cancer Genetics Group, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
C Diaz-de-HerediaDepartment of Pediatric Oncology and Hematology, Hospital Universitari Vall d'Hebron, Barcelona, Spain. crdiaz@vhebron.net.ORCID http://orcid.org/0000-0001-8086-296X
Vall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHematopoietic stem cell transplantation (HSCT) is a curative option for patients with Fanconi anemia (FA) and hematological manifestations but it does not prevent solid tumors, especially squamous cell carcinomas (SCC).

methodsRetrospective study in 22 FA patients who had received HSCT and had been followed up beyond 2 years after HSCT.

resultsThe median follow-up was 15 years. Six patients developed head-and-neck SCC after transplantation. The cumulative incidence of SCC at 15 and 30 years from the HSCT was 14.2% and 71.2%, respectively. One patient was diagnosed in stage IV and the rest, who were being followed up in cancer screening programs, in stage I. Treatment of SCC consisted of surgery in all patients; radiotherapy and chemotherapy were used in two patients and were poorly tolerated.

conclusionFA patients have high risk of head-and-neck SCC. Multi-disciplinary programs for early cancer detection are of special relevance in these patients.

Indexed as

Hematopoietic Stem Cell TransplantationAdultCarcinoma, Squamous CellFanconi AnemiaFemaleHead and Neck NeoplasmsHumansLongitudinal StudiesMalePostoperative ComplicationsRetrospective StudiesYoung AdultFanconi anemiaHead and neck squamous cell carcinomaHematopoietic stem cell transplantationMulti-disciplinary approach

Identifiers

PMID34417960
OpenAlexW3196173314

What OpenQuestion holds

Textmetadata
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.