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Observational Prospective Study of Quality of Life in Unresectable TNM Stage III NSCLC (OBSTINATE)

Active, not recruiting
Conditions
Non-Small Cell Lung Cancer
Interventions
Other: Quality of Life Questionnaire-Core 30 (QLQ-C30)
Registration Number
NCT05049044
Lead Sponsor
Groupe Francais De Pneumo-Cancerologie
Brief Summary

OBSTINATE is an observational, national, prospective, multicentric study on Quality of life in patients with unresecable stade III non-small cell lung cancers.

Locally advanced non-small cell lung cancers (NSCLCs with a Tumor, Node and Metastasis \[TNM\] stage III) patients represent approximately a third of newly discovered NSCLCs every year, and a very heterogeneous group of clinical situations. Therapies are multidisciplinary and very heterogeneous across oncology centers. Patients with locally advanced NSCLC have a high symptom burden that is known to affect their quality of life. Health-related quality of life (HR-QoL) is a specific and multidimensional type of patient-reported outcome (PRO) related to the physical, psychological and social impact of the disease and its treatment as perceived by patients. HR-QoL allows, together with data of efficacy and safety, a more complete assessment of risks and benefits of each treatment. Therefore, QoL maintenance is a valuable consideration for treatment decisions, especially in the rapidly evolving therapeutic landscape of unresectable NSCLC.

The study is designed to collect PROs HR-QoL data from every new patient diagnosed with an unresectable stage III NSCLC over a period of 18 months. We also aim to describe clinical characteristics of these patients, the therapeutic strategies conducted, and outcomes in a "real-word" oncological practice.

Detailed Description

OBSTINATE is an observational, prospective, national, multicentric study conducted in patients newly diagnosed with an unresectable stage III NSCLC (with exclusion of early stages NSCLC classified to pathological stage III).

OBSTINATE is a study planned to include 450 patients between 50 to 70 GFPC-affiliates or GFPC-associated centers approximately. All centers are located in France. The participating Site Investigators will be treating physicians within one of the participating centers.

After screening for eligibility checks, patients will receive the Patient Information Note from the Site Investigators. This Patient information Note will describe the study purpose and modalities. Patients who meet the eligibility criteria and do not oppose to data collection will be enrolled. The schedule of the medical visits in the study center will depend on the patient and his/her routine clinical care Protocol-relevant data will be collected by the treating physician within each center, for up to 5 years following the last patient's enrollment in the study.

Patients included in the study will complete the self-assess questionnaires at enrollment and during routine care follow-up, according to pre-specified data collection schedule.

Usual practices or modalities of follow-up of patients will remain unchanged compared to the current clinical practice as the study is designed to provide descriptive summary information.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
413
Inclusion Criteria
  • Pathological confirmation of NSCLC obtained from a tumor cytology or biopsy
  • Treatment-naïve unresectable TNM stage III NSCLC (according to the 8th TNM IASLC edition). Of note, unresectability could be due to either functional limitation or anatomical extension of the tumor.
  • Patient willing and able to complete collection of data via self-assessment questionnaires
  • Patient without any local or systemic anti-neoplastic treatment are eligible (palliative symptomatic radiotherapy is considered best supportive care)
  • Patients participating in other interventional or non-interventional studies can be included.
Exclusion Criteria
  • Early stage NSCLC initially treated locally (surgery or other) and classified as pathological TNM stage III (according to the 8th TNM IASLC edition)
  • At the treating physician's discretion, patient not eligible physically or psychologically to be included in a clinical trial
  • Inability to read and/or fill out self-assessment questionnaires
  • Patient unable to express opposition to data collection

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Cohort 8: IOQuality of Life Questionnaire-Core 30 (QLQ-C30)Immunotherapy only (IO)
Cohort 1: cRT-CT+IOQuality of Life Questionnaire-Core 30 (QLQ-C30)Concomitant radio-chemotherapy and consolidation immunotherapy (cRT-CT+IO)
Cohort 9: TTQuality of Life Questionnaire-Core 30 (QLQ-C30)Targeted therapy only (TT)
Cohort 10: BSCQuality of Life Questionnaire-Core 30 (QLQ-C30)Best supportive care only (BSC)
Cohort 2: sRT-CT+IOQuality of Life Questionnaire-Core 30 (QLQ-C30)Sequential radio-chemotherapy and consolidation immunotherapy (sRT-CT+IO)
Cohort 7: RTQuality of Life Questionnaire-Core 30 (QLQ-C30)Radiation therapy only (RT)
Cohort 5: CTQuality of Life Questionnaire-Core 30 (QLQ-C30)Chemotherapy only (CT)
Cohort 3: cRT-CTQuality of Life Questionnaire-Core 30 (QLQ-C30)Concomitant radio-chemotherapy (cRT-CT)
Cohort 4: sRT-CTQuality of Life Questionnaire-Core 30 (QLQ-C30)Sequential radio-chemotherapy (sRT-CT)
Cohort 6: CT+IOQuality of Life Questionnaire-Core 30 (QLQ-C30)Chemotherapy plus immunotherapy (CT+IO)
Primary Outcome Measures
NameTimeMethod
QLQ-LC13 (defined as the outcomes of a clinical intervention obtained by the patient)Up to 6,5 years (18 months of recruitment + 5 years). For Cohort 1 & 2, a follow-up post progression is planned

Change in patient's QLQ-LC13 during treatment and follow-up until confirmed progression, loss of follow-up or end of the study compared to Baseline in patients diagnosed with unresectable stage III NSCLC in a "real-world" oncological practice.

This evaluation is based on self-assess questionnaire distributed to the patients according to pre-specified data collection schedule.

The primary objective will be addressed in the cohort as a whole, and independently for every cohort of interest.

EQ5D-5L (defined as the outcomes of a clinical intervention obtained by the patient)Up to 6,5 years (18 months of recruitment + 5 years). For Cohort 1 & 2, a follow-up post progression is planned

Change in patient's EQ5D-5L during treatment and follow-up until confirmed progression, loss of follow-up or end of the study compared to Baseline in patients diagnosed with unresectable stage III NSCLC in a "real-world" oncological practice.

This evaluation is based on self-assess questionnaire distributed to the patients according to pre-specified data collection schedule.

The primary objective will be addressed in the cohort as a whole, and independently for every cohort of interest.

QLQ-C30 (defined as the outcomes of a clinical intervention obtained by the patient)Up to 6,5 years (18 months of recruitment + 5 years). For Cohort 1 & 2, a follow-up post progression is planned

Change in patient's QLQ-C30 during treatment and follow-up until confirmed progression, loss of follow-up or end of the study compared to Baseline in patients diagnosed with unresectable stage III NSCLC in a "real-world" oncological practice.

This evaluation is based on self-assess questionnaire distributed to the patients according to pre-specified data collection schedule.

The primary objective will be addressed in the cohort as a whole, and independently for every cohort of interest.

Secondary Outcome Measures
NameTimeMethod
Tumor characteristics as defined by mutational status of driver genesAt Baseline

Characterize the stage III unresectable NSCLC patients by mutational status of driver genes (e.g. epidermal growth factor receptor \[EGFR\]) anaplastic lymphoma kinase \[ALK\], reactive oxygen species 1 \[ROS1\], human epidermal growth factor receptor 2 \[HER2\], PI3KCA, BRAF, MET, rearranged during transfection \[RET\], neurotrophic receptor tyrosine kinase \[NRTK\])

Median OS (e.g. median PFS, median OS)From date of first treatment administration up to first documented disease progression and/or death from any cause, whichever came first, assessed up to 60 months

Time from date of first treatment administration until the date of first documented progression or date to death from any cause, whichever came first as evaluated by investigators.

Tumor characteristics as defined by PD-L1 expression statusAt Baseline

Characterize the stage III unresectable NSCLC patients by PD-L1 expression status (tumor propensity score)

Time from diagnosis to treatmentFrom date of diagnosis until the date of first documented treatment or start date of best supportive care through study completion, up to 5 year
Modality of follow-upFrom date of diagnosis until the date of first documented progression or or date of death from any cause, whichever came first, assessed up to 5 years maximum

Description of modality of follow-up (e.g. type of imagery used, frequency of medical visit)

Duration of response of treatmentFrom date of first treatment administration up to end of study, assessed up to 5 years maximum
Toxicity of treatmentFrom date of first treatment administration up to end of study, assessed up to 5 years maximum

limited to Cohorts 1, 2, 3 and 4 (restricted to significant AEs, which include but are not limited to: serious AEs \[SAEs\], AEs that led to treatment discontinuation, or any AEs ≥ grade 3 judged clinically significant by the Site Investigator)

Baseline demographicsAt Baseline

Stage III unresectable NSCLC patients characteristics: baseline patient demographics at stage III NSCLC diagnosis, clinical, pathological and molecular characteristics (e.g. age, race, comorbidities)

Tumor characteristics as defined by TNM stageAt Baseline

Characterize the stage III unresectable NSCLC patients by TNM stage according to the 8th TNM IASLC edition

Treatment characteristicsFrom date of first treatment administration up to end of study, assessed up to 5 years maximum

Describe the chemotherapy, radiation therapy and immunotherapy protocols used (e.g. dose, reduction, interruptions, duration)

Effective treatment compared to initial Multidisciplinary Tumor Board (MDTB) decisionFrom date of first treatment administration up to end of study, assessed up to 5 years maximum

Concordance between effective treatment compared to initial MDTB decision

Type of progression (local, loco-regional, metastatic)At date of first documented progression, assessed up to 5 years maximum
Median PFSFrom date of first treatment administration up to first documented disease progression and/or death from any cause, whichever came first, assessed up to 60 months

Time from date of first treatment administration until the date of first documented progression or date to death from any cause, whichever came first as evaluated by investigators.

Best response of treatmentFrom date of first treatment administration up to end of study, assessed up to 5 years maximum
Description of second line of treatment after disease progressionFrom date of first documented progression up to end of study, assessed up to 5 years maximum

Treatment characteristics after disease progression including type of treatment (chemotherapy, radiotherapy, immunotherapy or Tyrosine-Kinase inhibitors), treatment duration, stop date of treatment and reason for end of treatment

Change in patients' socio-economic and occupational outcomes using unique self questionnaireFrom Baseline, during treatment and follow-up until confirmed progression (of note, for Cohorts 1 and 2, a follow-up post-progression is planned), loss of follow-up or end of the study, assessed up to 5 years maximum

Change in patients' socio-economic and occupational outcomes during treatment and follow-up until confirmed progression (of note, for Cohorts 1 and 2, a follow-up post-progression is planned), loss of follow-up or end of the study using a dedicated self questionnaire on socio-economic and occupational outcomes

Median time to progressionFrom date of first treatment administration up to first documented disease progression and/or death from any cause, whichever came first, assessed up to 60 months

Time from date of first treatment administration until the date of first documented progression or date to death from any cause, whichever came first as evaluated by investigators.

Evaluate the cost-utility of the therapeutic strategy using Quality-Adjusted Life Years (QALYs)From Baseline, during treatment and follow-up until confirmed progression (of note, for Cohorts 1 and 2, a follow-up post-progression is planned), loss of follow-up or end of the study, assessed up to 5 years maximum

Trial Locations

Locations (36)

Hôpital du Scorff

🇫🇷

Lorient, France

Centre Hospitalier Intercommunal de Quimper

🇫🇷

Quimper, France

Institut Lucien Neuwirth

🇫🇷

Saint-Priest-en-Jarez, France

Hôpital Paul d'Egine

🇫🇷

Champigny-sur-Marne, France

Centre Hospitalier Universitaire

🇫🇷

Angers, France

Centre Hospitalier d'Aix en Provence

🇫🇷

Aix En Provence, France

Hôpital Robert Boulin

🇫🇷

Libourne, France

CHU Ponchaillou

🇫🇷

Rennes, France

Clinique Mutualiste de l'Estuaire

🇫🇷

Saint Nazaire, France

CH de Bigorre Tarbes

🇫🇷

Tarbes, France

CHU Amiens-Picardie

🇫🇷

Amiens, France

Centre Hospitalier Universitaire DUPUYTREN

🇫🇷

Limoges, France

Centre Hospitalier Régional

🇫🇷

Orléans, France

Hôpital Privé de la Loire

🇫🇷

Saint-Étienne, France

CHU Hôpital Nord

🇫🇷

Saint-Étienne, France

Hôpital Privé d'Antony

🇫🇷

Antony, France

Centre Hospitalier du Morvan

🇫🇷

Brest, France

Centre Hospitalier du Cotentin

🇫🇷

Cherbourg, France

Centre Hospitalier Intercommunal de Créteil

🇫🇷

Creteil, France

Hôpital de Meaux

🇫🇷

Meaux, France

Centre Hospitalier de Villefranche sur Saone

🇫🇷

Villefranche Sur Saone, France

Centre Hospitalier de Chauny

🇫🇷

Chauny, France

CHD Les Oudairies

🇫🇷

La Roche-sur-Yon, France

Hôpital Européen

🇫🇷

Marseille, France

Centre Catalan d'Oncologie

🇫🇷

Perpignan, France

Hôpital d'Instruction des Armées Ste Anne

🇫🇷

Toulon, France

CH Bretagne Atlantique

🇫🇷

Vannes, France

Centre hospitalier Intercommunal

🇫🇷

Villeneuve-Saint-Georges, France

CHU La Réunion Site Sud

🇫🇷

Saint-Pierre, France

Centre Hospitalier d'Annecy

🇫🇷

Annecy, France

CHMS

🇫🇷

Chambéry, France

Centre Hospitalier d'Elbeuf - Pneumologie

🇫🇷

Elbeuf, France

Centre Leon Bérard

🇫🇷

Lyon, France

Hôpital Nord

🇫🇷

Marseille, France

Hôpital Charles Nicolle

🇫🇷

Rouen, France

CHU La Réunion Site Nord

🇫🇷

Saint-Denis, France

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