Evidence map›Paper›PMID 32691271›Full record

ReviewEndocrine2021

Long-term follow-up and safety of vandetanib for advanced medullary thyroid cancer.

Helton Estrela Ramos, Fabio Hecht, Amandine Berdelou, Isabelle Borget, Sophie Leboulleux, Eric Baudin, Martin Schlumberger

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Systemic therapies for medullary thyroid carcinoma: state of the art.Therapeutic advances in endocrinology and metabolism · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Precision oncology forFrontiers in oncology · 2022
    Review
  13. Current Guidelines for Management of Medullary Thyroid Carcinoma.Endocrinology and metabolism (Seoul, Korea) · 2021
    Review
  14. Review
  15. 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.

Helton Estrela RamosDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France. ramoshelton@gmail.com.ORCID http://orcid.org/0000-0002-2900-2099
Fabio HechtDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Amandine BerdelouDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Isabelle BorgetDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Sophie LeboulleuxDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Eric BaudinDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Martin SchlumbergerDepartment of Nuclear Medicine and Endocrine Oncology, Gustave Roussy, Villejuif, France.
Institut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionVandetanib is indicated for adults with advanced medullary thyroid cancer (MTC).

objectivesTo describe the efficacy and toxicity profile of vandetanib treatment with a maximal follow-up of 11 years at Institut Gustave Roussy/France.

methodsA review of the clinical files of the 76 MTC patients treated with vandetanib. Efficacy was estimated by markers and imaging.

resultsA total of 76 patients received vandetanib. Nine were excluded from efficacy analysis because lack of morphological data. The overall (N = 76) median treatment duration was 17.6 (range: 0.7-130.6) months and the median progression-free survival (PFS) was 22.7 (95% CI, 13.9-37.3) months. In total, 21/76 (27.6%) patients were classified as long-term users because have received vandetanib for more than 48 months, with a median treatment duration of 68.1 (range: 49.1-130.6) months. For long-term vandetanib users, the objective response rate was 85.7%, the median time to best response was 27.8 (11.6.1-110) months and the median duration of response was 70.4 (38.3-127.5) (95% CI 49.5-102.8) months with a median PFS of 73.2 (95% CI, 53.1-105.6) months. Duration of response had a significant negative correlation with patient age at diagnosis (p = 0.03) and was significantly higher in patients that did not have confirmed tumor progression before treatment onset (p = 0.007). After 48 months of vandetanib use, renal failure took place in two patients and heart failure, cholecystitis, acute pancreatitis, posterior encephalopathy, and skin cancer first occurred in one patient, each.

conclusionsOur findings suggest that a substantial number of patients receiving first-/second-line vandetanib may sustain long clinical benefit and that a younger age at diagnosis and the absence of progression before treatment could be considered as predictors of durable response.

Indexed as

Antineoplastic AgentsCarcinoma, NeuroendocrinePancreatitisThyroid NeoplasmsAcute DiseaseAdultDisease-Free SurvivalFollow-Up StudiesFranceHumansPiperidinesQuinazolinesAntineoplastic AgentsPiperidinesQuinazolinesvandetanibLong-useMedullary thyroid cancerVandetanib

Identifiers

PMID32691271
OpenAlexW3045183004

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.