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NCT Number: NCT05789667

Gender-based Impact on Safety and Efficacy of Lenvatinib in Patients With Differentiated Thyroid Cancer

Lenvatinib is approved for the treatment of radioiodine refractory differentiated thyroid cancer. Despite gender can play a crucial role un in safety and efficacy of oncological product, little is know on gender difference in lenvatinb effacacy and safety in the context of radioiodine refractory differentiated thyroid cancer.

The primary objective of the study is to assess safety and toxicity profile in male and female patients in terms of dose reduction. The secondary objectives are to assess sex and gender difference in: the number and the incidence of adverse events; response rate according to RECIST criteria 1.1; progression free survival, overall survival and duration of response.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Regina Elena National Cancer Institute

Rome, 00144, Italy

Location status: Recruiting

Location contact

Marialuisa Appetecchia, MD

CONTACT

[email protected]

0039 0652666026

About this study

Lenvatinib is an orally available potent inhibitor of the split-kinase family of transmembrane growth factor receptors including Flt-1/VEGFR-1 and KDR/VEGFR. Lenvatinib has been investigated in hepatocellular carcinoma and in RAI-resistant thyroid cancer (Phase III trials) and in other malignancies, showing high rates of activity. In RAI-resistant thyroid cancer, lenvatinib showed a remarkable response rate over placebo (65% vs 2), combined with a prolonged progression free survival (18.3 vs 3.6 months). It has been approved for the treatment of locally recurrent or metastatic, progressive RAI resistance-DTC in the United States, Europe, and Japan, based on the results from SELECT trial. Moreover, lenvatinib demonstrated a meaningful clinical activity (response rate 64.8% in treatment arm vs 1.5% in placebo arm, p<0.001;) significantly reducing the tumour burden, with a median maximum percentage change in tumour size of -42.9%. Response was mostly pronounced at the first assessment (median -24.7% at 8 weeks after randomization) but it has been observed even in the following months (-1.3% per month). Recently, the efficacy of lenvatinib was confirmed in specific patient population, such as elderly. Although the efficacy is remarkable toxic effects are considerable and not all patients have the same risk to benefit ratio from lenvatinib treatment. Results derived from controlled clinical trials are rarely replicable in the real-life because these trials are usually conducted in selected populations, in a highly controlled setting, optimized to show the effect of the drug.

In this context growing evidences are showing gender associated functions playing a role in cancer incidence, progression and response to therapy; gender disparities in toxicities and effectiveness of certain drugs used in the treatment of the most common cancer is already well known.The aim of the present study is to evaluate the safety and efficacy profile of Lenvatinib based on gender in patients with refractory iodine DTC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with refractory iodine DTC treated with lenvatinib
  • Signed written informed consent

Exclusion criteria

  • Age < 18 years

Treatment and study plan

Lenvatinib

Drug

Patients will be treated by lenvatinib as recommended by good clinical practice

Other names: lenvatinib mesilate, Lenvatinib Oral Capsule [Lenvima]

Primary outcomes

  1. Gender difference in Safety profile of lenvatinib treatment

    Time frame: 1 year

    Difference in lenvatinib dose reduction between male and female patients

Secondary outcomes

  1. Gender difference in lenvatinib side effects incidence

    Time frame: 1 year

    Difference in number of lenvatinib side effects between male and female patients according to CTCAE 5.0

  2. Gender difference in lenvatinib response rate

    Time frame: 1 year

    Difference in lenvatinib response rate (CR+PR) according to RECIST response evaluation criteria 1.1 in male and female patients.

  3. Gender difference progression free survival and overall survival of patients treated with lenvatinib

    Time frame: 1 year

    Difference in progression free survival and overall survival of patients treated with lenvatinib in male and female patients.

Study contacts

Contact information is provided by the study sponsor or research team.

Marialuisa Appetecchia, Prof

CONTACT

[email protected]

00390652666026

Sponsors and collaborators

Lead sponsor

Regina Elena Cancer Institute

Other

Collaborators

  • Istituto Auxologico Italiano
  • Istituto Oncologico Veneto IRCCS
  • University of Catania
  • University of Pisa
  • University of Roma La Sapienza
  • University of Siena
  • University of Turin, Italy

Registry information

Official study title

Observational Study on Gender-based Impact on Safety and Efficacy of Lenvatinib in Patients With Radioiodine Refractory Differentiated Thyroid Cancer

Acronym: Gisel

Important dates

Study start
2020
Primary completion
2024
Study completion
2025
First posted
Mar 29, 2023
Registry last updated
Dec 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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