Evidence map›Paper›PMID 38683497›Full record

ArticleJournal of endocrinological investigation2024

Improved overall survival in patients developing endocrine toxicity during treatment with nivolumab for advanced non-small cell lung cancer in a prospective study.

M Albertelli, G Rossi, E Nazzari, C Genova, F Biello, E Rijavec, M G Dal Bello, L Patti, M Tagliamento, G Barletta and 6 more

Abstract read
In one paragraph

Article in Journal of endocrinological investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

16 authors.

M Albertelli *Endocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy. manuela.albertelli@unige.it.ORCID http://orcid.org/0000-0002-5957-3247
G Rossi *Lung Cancer Unit, Department of Oncology, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
E NazzariEndocrinology Unit, Department of Internal Medicine and Medical Specialties (DiMI), University of Genova, Viale Benedetto XV, 6, 16132, Genova, Italy.
C GenovaAcademic Oncology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
F BielloDivision of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
E RijavecUnit of Medical Oncology, Department of Medicine and Surgery, University of Insubria, ASST dei Sette Laghi, Varese, Italy.
M G Dal BelloLung Cancer Unit, Department of Oncology, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
L PattiEndocrinology Unit, Department of Internal Medicine and Medical Specialties (DiMI), University of Genova, Viale Benedetto XV, 6, 16132, Genova, Italy.
M TagliamentoAcademic Oncology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
G BarlettaLung Cancer Unit, Department of Oncology, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
P MorabitoLung Cancer Unit, Department of Oncology, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
M BoschettiEndocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
A DottoEndocrinology Unit, Department of Internal Medicine and Medical Specialties (DiMI), University of Genova, Viale Benedetto XV, 6, 16132, Genova, Italy.
D CampanaUO Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
D FeroneEndocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
F GrossiUnit of Medical Oncology, Department of Medicine and Surgery, University of Insubria, ASST dei Sette Laghi, Varese, Italy.

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca FIRB RBAP11884M
6 · The paper itself

Abstract

purposeImmune checkpoint inhibitors (ICPIs) disrupting PD-1/PD-L1 axis have revolutionized the management of advanced non-small cell lung cancer (NSCLC). Some studies identified the development of endocrine toxicity as predictor of better survival in cancer patients treated with ICPIs. The aim of study was to evaluate survival and new onset of immune-related endocrine adverse events (irAEs) in patients treated with nivolumab for advanced NSCLC.

methodsIn a prospective study, 73 patients with previously treated advanced NSCLC received nivolumab in monotherapy. Blood samples were collected at each cycle to monitor thyroid autoimmunity, thyroid, adrenal and somatotroph axes, while thyroid morphology was evaluated by ultrasonography.

resultsAn impaired thyroid function was recorded in 23.4% of patients (n = 15). Eight patients developed asymptomatic transient thyrotoxicosis (ATT) evolving to hypothyroidism in 50% of cases. In addition, seven patients developed overt hypothyroidism without ATT and with negative autoantibodies. Patients who developed hypothyroidism proved to have better overall survival (OS) as compared with non-developers at both univariate (p = 0.021) and multivariate analyses (p = 0.023). The survival curve of patients with reduced IGF-I at baseline, or displaying its reduction during the follow-up, showed significantly reduced median survival compared to patients with normal/high IGF-I levels (p = 0.031).

conclusionsThyroid function abnormalities are the major irAEs in patients treated with nivolumab, and hypothyroidism onset is associated with prolonged survival. Our findings indicate that the development of hypothyroidism is a positive predictive biomarker of nivolumab antitumor efficacy in patients with NSCLC. Low IGF-I levels could represent a negative prognostic factor during nivolumab therapy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsNivolumabAdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalEndocrine System DiseasesFemaleFollow-Up StudiesHumansHypothyroidismImmune Checkpoint InhibitorsMaleMiddle AgedPrognosisAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsNivolumabEndocrine toxicityHypothyroidismNivolumabNSCLCOverall survival

Identifiers

PMID38683497
PMCPMC11196302

What OpenQuestion holds

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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.