Evidence map›Paper›PMID 27704480›Full record

ArticleEndocrine2017

Long-term outcome of multimodal therapy for giant prolactinomas.

Paula Andujar-Plata, Rocio Villar-Taibo, Maria Dolores Ballesteros-Pomar, Alfonso Vidal-Casariego, Begoña Pérez-Corral, Jose Manuel Cabezas-Agrícola, Paula Álvarez-Vázquez, Ramón Serramito, Ignacio Bernabeu

Abstract read
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In one paragraph

Article in Endocrine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Long-term Follow-up of 84 Patients With Giant Prolactinomas-A Swedish Nationwide Study.The Journal of clinical endocrinology and metabolism · 2023
    Article
  4. Review
  5. Surgical Management of Giant Prolactinomas: A Descriptive Study.International journal of endocrinology · 2023
    Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Review
  11. 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

9 authors at 4 institutions in 1 country.

Paula Andujar-PlataEndocrinology Division, Complejo Hospitalario Universitario de Ourense (CHUO)-SERGAS, Ourense, 32005, Spain.
Rocio Villar-TaiboComplejo Asistencial Universitario de León (CAULE)-SACYL, León, 24008, Spain.
Maria Dolores Ballesteros-PomarComplejo Asistencial Universitario de León (CAULE)-SACYL, León, 24008, Spain.
Alfonso Vidal-CasariegoComplejo Asistencial Universitario de León (CAULE)-SACYL, León, 24008, Spain.
Begoña Pérez-CorralComplejo Asistencial Universitario de León (CAULE)-SACYL, León, 24008, Spain.
Jose Manuel Cabezas-AgrícolaEndocrinology Division, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS)-SERGAS, Santiago de Compostela, 15706, Spain.
Paula Álvarez-VázquezEndocrinology Division, Complejo Hospitalario Universitario de Ourense (CHUO)-SERGAS, Ourense, 32005, Spain.
Ramón SerramitoNeurosurgery Division, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS)-SERGAS, Santiago de Compostela, 15706, Spain.
Ignacio BernabeuEndocrinology Division, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS)-SERGAS, Santiago de Compostela, 15706, Spain. ignacio.bernabeu.moron@sergas.es.
Complejo Asistencial Universitario de Palencia · ESComplejo Hospitalario Universitario de Santiago · ESComplejo Hospitalario de Ourense · ESServicio Gallego de Salud · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giant prolactinomas are rare tumors characterized by their large size, compressive symptoms, and extremely high prolactin secretion. The aim of this study is to describe our experience with a series of 16 giant prolactinomas cases in terms of clinical presentation, therapeutic decisions, and final outcomes. Retrospective analysis of adult patients diagnosed with giant prolactinomas at the endocrine departments of three university tertiary hospitals. We included 16 patients (43.7 % women); mean age at diagnosis: 42.1 ± 21 years. The most frequent presentation was compressive symptoms. The delay in diagnosis was higher in women (median of 150 months vs. 12 in men; p = 0.09). The mean maximum tumor diameter at diagnosis was 56.9 ± 15.5 mm, and mean prolactin levels were 10,995.9 ± 12,157.8 ng/mL. Dopamine agonists were the first-line treatment in 11 patients (mean maximum dose: 3.9 ± 3.2 mg/week). Surgery was the initial treatment in five patients and the second-line treatment in six. Radiotherapy was used in four cases. All patients but one, are still with dopamine agonists. After a mean follow-up of 9 years, prolactin normalized in 7/16 patients (43.7 %) and 13 patients (81 %) reached prolactin levels lower than twice the upper limit of normal. Mean prolactin level at last visit: 79.5 ± 143 ng/mL. Tumor volume was decreased by 93.8 ± 11.3 %, and final maximum tumor diameter was 18.4 ± 18.8 mm. Three patients are actually tumor free. Giant prolactinomas are characterized by a large tumor volume and extreme prolactin hypersecretion. Multimodal treatment is frequently required to obtain biochemical and tumor control.

Indexed as

RadiotherapyAdultCombined Modality TherapyDopamine AgonistsFemaleHumansMaleMiddle AgedNeurosurgical ProceduresPituitary GlandPituitary NeoplasmsProlactinProlactinomaTreatment OutcomeYoung AdultDopamine AgonistsProlactinCabergolineGiant prolactinomaPituitary adenomaProlactin

Identifiers

PMID27704480
OpenAlexW2529225537

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.