Role of PET Scan in the Evaluation of Early Response to Maintenance Treatment in Advanced Non-small-cell Lung Cancer (CALMETTE)

Centre Henri Becquerel

Status and phase: Unknown; Phase 2

Conditions: Non-small Cell Lung Cancer

Treatments: Procedure: PET scan imaging

Study type: Interventional

Funder types: Other

Identifiers

NCT02507518

CHB12.01

Details and patient eligibility

About

Non small cell lung cancer is the first cause of cancer related death in France and is becoming an increasing health problem in developing countries.

Recently for patient with no progression disease after first line chemotherapy, new therapies were validated in maintenance (bevacizumab) or switch maintenance treatment (erlotinib, pemetrexed) with improved survival.

Until now, determination of efficiency of treatment is only based on morphological response (RECIST) and remains inappropriate to such cytostatic drugs for which there is no anatomical lesion modification.

Nuclear Medicine and especially 18-FDG Positron Emission Tomography (PET) offers a biologically relevant tool for assessment of tumour response therapies.

The assumption of the study is that FDG PET would allow to earlier detect a lack of response, thereafter, to modify an ineffective treatment. Indeed, nowadays the treatment is maintained up to evidence of progression disease.

However, despite the increasing use of FDG PET for predicting therapeutic response, there are no validated criteria for judging response of maintenance therapy in non-small cell lung cancer.

It seems necessary to determine standardized criteria response, earlier during the course of maintenance therapy in patient with non small cell lung cancer.

The final aim is to optimize survival by an adapted metabolic imaging guided therapy.

Full description

The purpose of the study is to optimize survival by an adapted metabolic imaging therapy in patients with advances non-small cell lung cancer.

The primary objective of the study is to evaluate the role of SUV and metabolic volume measured by FDG PETScan in the early prediction of treatment response.

80 patients will be included in 2 years. They will be follow up for one year for monitoring the progression free survival.

Enrollment: 80 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age superior to 18 years old
• Effective contraception method or negative pregnancy test at the inclusion
• OMS inferior or equal to 1
• Non-small cell lung cancer stage IIIb or IV
• Non progressive disease after at lest 4 cycles of platinum-based chemotherapy
• Eligible fo maintenance therapy with bevacizumab and/or pemetrexed
• Inform consent signed

Exclusion criteria

• Evolution of a second cancer in the 3 years before inclusion
• Pregnancy or breast-feeding
• poorly controlled diabetes
• curatorship or guardianship
• contraindication to iodinated contrast agents
• participation to another clinical research with an experimental drug
• impossible decubitus
• not possibility to follow-up the procedures of the study due to geographic, social or psychic reasons

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

80 participants in 1 patient group

Experimental

Experimental group

Description:

Two Pet scan Imaging will be done : 14 days before and 16 days after the beginning of maintenance therapy

Treatment:

Procedure: PET scan imaging