Survival Without Persistent Limiting Toxicity: Real Life Prospective Cohort of Advanced Neuroendocrine Tumor

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGustave Roussy, Cancer Campus, Grand Paris

About this trial

Advanced neuroendocrine tumors (NETs) are rare cancers, characterized by prolonged survival (median\>5 years). If five medical options are now approved and 4 others are only recommended, the best sequence is still unknown. No single study on long-term cumulative toxicity of consecutive treatment interventions has been published so far. Taking into account real-world context is required for sound decision- making that cannot be answered by randomized trials.

Project objectives and brief description of the methods, which will be used to achieve them: Study team will construct a longitudinal prospective cohort of consecutive non resectable or metastatic NET patients using the GTE-RENATEN network to evaluate the real world cumulative and limiting toxicities. They will expect, as primary endpoint, a difference in survival without limiting (\>grade 1 adverse event according to nci.ctc V5) persistent (\>6 months) toxicity between therapeutics classes or therapeutics sequences in the real life conditions all along the treatments lines, since metastasis diagnosis. All NET primary patients will be enrolled.

Patients will be followed until the primary endpoint is reached, death or until 5 years.

Based on our pilot study, we plan to enroll 1100 patients to detect 150 events and adjust for 15 cofounders and 10% of lost to follow-up. Cox model adapted to time-related dependency will be used to analyze the data and machine learning will be utilized to take into account the number of confounding factors, interactions and nonlinear relationship. The best model of prediction will be validated in a subgroup of the cohort population.

Expected results: Study team will create a tool to help therapeutic decision in order to identify in a given patient the best therapeutic class or sequence with the lowest risk of persistent limiting toxicity.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Unresectable local or metastatic NET naive of treatment tumor except somatostatin analogues or primary surgery.

Unresectable local or metastatic NET newly diagnosed<6 months whatever the primary NET site

Well differentiated neuroendocrine tumor (WHO classifications) pathologically reviewed locally

No initial medical absolute contraindication to any of the authorized or recommended treatments (no AE>grade 1 according to NCI CTC v.5 criteria),

Disqualifiers

Patients with severe illness that contraindicates participation to any study

Age <18 years old

Trial population

unresectable or metastatic NET patients

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • quality of life questionnaire, treatment side effect follow up

    Other intervention

    decrire

Treatment groups

1,100 Participants
are divided into 1 treatment group
Group A: TOLERATE cohort1 intervention

Trial outcomes

Primary outcomes

1

Survival without persistent limiting toxicity

To determine the survival of unresectable or metastatic NET patients without limiting persistent toxicity (SPLT) in order to obtain decision support for the best therapeutic class or sequence depending on the patient and the treatments received

Time frame
"From enrollment to the end of follow up at 5 years"

Secondary outcomes

1

Survival without persistent limiting toxicity according to nci.ctc v.5 grade 3 or 4 adverse events

To evaluate the survival without persistent limiting toxicity according to nci.ctc v.5 grade 3 or 4 adverse events

Time frame
"From enrollment to the end of follow up at 5 years"
2

Survival without persistent, defined above 3 months, limiting toxicity according to nci.ctc v.5 grade >1 adverse events

To analyze the survival without persistent, defined above 3 months, limiting toxicity according to nci.ctc v.5 grade \>1 adverse events

Time frame
"From enrollment to the end of follow up at 5 years"
3

Best treatment line sequencing

Best treatment line sequencing in terms of maximizing SPLT after adjustment to comorbidity, modality of follow-up and prognostic parameters

Time frame
"From enrollment to the end of follow up at 5 years"
4

Duration of each active treatment

To analyze the duration of each active treatments and therapeutic breaks

Time frame
"From enrollment to the end of follow up at 5 years"

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: