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FLT3 LigandWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (7)


Name (Synonyms) Correlation
drug2508 SBRT Wiki 1.00
drug3176 anti-CD40 antibody Wiki 1.00
drug757 Convalescent Plasma Transfusion Wiki 0.71
drug1433 Interferon Beta-1A Wiki 0.50
drug812 DAS181 Wiki 0.41
drug1489 Ivermectin Wiki 0.22
drug1284 Hydroxychloroquine Wiki 0.10

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D002289 Carcinoma, Non-Small-Cell Lung NIH 0.71
D008175 Lung Neoplasms NIH 0.45

Correlated HPO Terms (2)


Name (Synonyms) Correlation
HP:0030358 Non-small cell lung carcinoma HPO 0.71
HP:0100526 Neoplasm of the lung HPO 0.45

There is one clinical trial.

Clinical Trials


1 FLT3 Ligand, CD40 Agonist Antibody, and Stereotactic Radiotherapy Versus Standard Therapy for Advanced Non-small Cell Lung Cancer: A Phase I/II Randomized Trial

The purpose of this study is to test a new way of treating the most common form of lung cancer. The investigators are testing a combination of radiotherapy with two new forms of immunotherapy. This study is testing the safety and effectiveness of this treatment approach as compared to standard treatment options.

NCT04491084 Non Small Cell Lung Cancer Lung Cancer Drug: FLT3 Ligand Biological: anti-CD40 antibody Radiation: SBRT
MeSH:Lung Neoplasms Carcinoma, Non-Small-Cell Lung
HPO:Neoplasm of the lung Non-small cell lung carcinoma

Primary Outcomes

Description: Death Any ≥ Grade 3 non-hematological toxicity, with the following exceptions: Grade 3 alopecia, vitiligo, or endocrinopathies controlled by hormone replacement therapy Grade 3 nausea that resolves to ≤ grade 2 with or without treatment within 72 hours Grade 3 vomiting and diarrhea that resolves to ≤ grade 2 with or without treatment within 72 hours Grade 3 fatigue that resolves to ≤ grade 2 within 5 days Grade 3 hypertension in the absence of maximal medical therapy Grade 3 adverse event of tumor flare (defined as local pain, irritation, or rash localized at sites of known or suspected tumor) of ≤ 7 days in duration Grade 3 amylase or lipase abnormalities that are not associated with symptoms or clinical manifestations of pancreatitis. It is recommended to consult with the Principal Investigator for grade 4 amylase or lipase abnormalities Grade 3 clinically significant laboratory abnormalities that are asymptomatic and can be reversed within 72 hours, however: Any Grade 4

Measure: Phase I: Dose-limiting toxicity (DLT), defined as follows:

Time: up to 8 weeks after initiation of study therapy

Measure: Phase II: Progression-free survival (PFS) duration

Time: defined as time from study registration until disease progression (scored using iRECIST) or death, whichever comes first up to 51 weeks.

Secondary Outcomes

Description: Length of time that patient survives from time of study registration

Measure: Overall survival (OS) duration

Time: From date of registration until the date of death from any cause, assessed up to 2 years

Description: The clinical benefit rate (CBR) will be defined as the percentage of subjects who achieve best response of confirmed CR or PR, or stable disease (SD) for at least four months.

Measure: Radiographic responses using descriptive statistics

Time: From date of registration, assessed up to 4 months

Description: Summary statistics (mean, standard deviation, median, 25th and 75th percentiles, and range) and the mean change from baseline of linear-transformed scores will be reported for all the items and subscales of the EORTC QLQ-C30 questionnaire and the QLQ-LC13, according to the EORTC scoring manual guidelines. higher scores are a better level of functioning

Measure: Quality of Life using EORTC QLQ-LC13 (quality of Life Questionnaire, Lung Cancer)

Time: 1 year

Description: Summary statistics (mean, standard deviation, median, 25th and 75th percentiles, and range) and the mean change from baseline of linear-transformed scores will be reported for all the items and subscales of the EORTC QLQ-C30 questionnaire and the QLQ-LC13, according to the EORTC scoring manual guidelines. Most items are scored 1 to 4, higher scores are a better level of functioning.

Measure: Quality of Life using QLQ-C30 (Quality of Life Questionnaire)

Time: 1 year

Description: Average daily step counts

Measure: Daily step count using descriptive statistics

Time: 1 year


Related HPO nodes (Using clinical trials)