Evidence map›Paper›PMID 33112279›Full record

ArticleEuropean journal of endocrinology2021

Immune checkpoint inhibitor therapy for ACTH-secreting pituitary carcinoma: a new emerging treatment?

Bastiaan Sol, Jeroen M K de Filette, Gil Awada, Steven Raeymaeckers, Sandrine Aspeslagh, C E Andreescu, Bart Neyns, Brigitte Velkeniers

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in European journal of endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
5.8field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Therapy for aggressive pituitary tumors and carcinomas.Reviews in endocrine & metabolic disorders · 2026
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  17. Aggressive Pituitary Tumors and Pituitary Carcinomas: From Pathology to Treatment.The Journal of clinical endocrinology and metabolism · 2023
    Article
  18. Tumour microenvironment and pituitary tumour behaviour.Journal of endocrinological investigation · 2023
    Review
  19. Review
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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

8 authors at 1 institution in 1 country.

Bastiaan SolDepartment of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
Jeroen M K de FiletteDepartment of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
Gil AwadaDepartment of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
Steven RaeymaeckersDepartment of Radiology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.ORCID 0000-0003-0822-1919
Sandrine AspeslaghDepartment of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
C E AndreescuDepartment of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
Bart NeynsDepartment of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.
Brigitte VelkeniersDepartment of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.ORCID 0000-0001-8577-9698
Universitair Ziekenhuis Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPituitary carcinomas are rare but aggressive and require maximally coordinated multimodal therapies. For refractory tumors, unresponsive to temozolomide (TMZ), therapeutic options are limited. Immune checkpoint inhibitors (ICI) may be considered for treatment as illustrated in the present case report. CASE: We report a patient with ACTH-secreting pituitary carcinoma, progressive after multiple lines of therapy including chemotherapy with TMZ, who demonstrated disease stabilization by a combination of ipilimumab (anti-CTLA-4) and nivolumab (anti-PD-1) ICI therapy. DISCUSSION: Management of pituitary carcinoma beyond TMZ remains ill-defined and relies on case reports. TMZ creates, due to hypermutation, more immunogenic tumors and subsequently potential candidates for ICI therapy. This case report adds support to the possible role of ICI in the treatment of pituitary carcinoma.

conclusionICI therapy could be a promising treatment option for pituitary carcinoma, considering the mechanisms of TMZ-induced hypermutation with increased immunogenicity, pituitary expression of CTLA-4 and PD-L1, and the frequent occurrence of hypophysitis as a side effect of ICI therapy.

Indexed as

ACTH-Secreting Pituitary AdenomaAdenomaAdultAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCarcinomaCell Cycle CheckpointsHumansIpilimumabMaleNivolumabAntineoplastic Agents, ImmunologicalIpilimumabNivolumab

Identifiers

PMID33112279
PMCPMC7707801
OpenAlexW3092023225

What OpenQuestion holds

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LicenceCC BY
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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.