Etude : ATLANTIS PM 01183 /



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Acronyme
Nom
Traitement
Type d'étude
MÀJ
Présentation de l'étude
Acronyme : ATLANTIS PM 01183

Nom :

Traitement : Adjuvant

Type d'étude : Hors ciblage moléculaire

Dernière MÀJ : 07/11/2017
Titre
Spécialité(s)
CIM10 - Localisation(s)
Informations principales
Titre : Essai clinique de phase III, randomisé, comparant l'association Lurbinectedine (PM01183) / Doxorubicine (DOX) à l'association Cyclophosphamide (CTX) / Doxorubicine (DOX) / Vincristine (VCR) ou Topotécan comme traitement chez des patients présentant un cancer bronchique à petites cellules (CBPC) après échec à une ligne de traitement antérieur à base de platine

Spécialité : Organes respiratoires et intrathoraciques
Localisation : C34 - Tumeur maligne des bronches et du poumon
Schéma
Phase
Stade
Ligne(s)
Informations complémentaires
Schéma : Phase III Randomized Clinical Trial of Lurbinectedin (PM01183)/Doxorubicin (DOX) Versus Cyclophosphamide (CTX), Doxorubicin (DOX) and Vincristine (VCR) (CAV) or Topotecan as Treatment in Patients With Small-Cell Lung Cancer (SCLC) Who Failed One Prior Platinum-containing Line

3 arms:
- Experimental: Lurbinectedin (PM01183) / Doxorubicin
- Active Comparator / Control 1: CAV (Cyclophosphamide (CTX), Doxorubicin (DOX) and Vincristine (VCR))
- Active Comparator / Control 2: Topotecan

Phase : III

Stade : NA

2
Critères d'inclusion
Critères de non-inclusion
Critères d'inclusion et de non-inclusion
Critères d'inclusion : - Voluntary written informed consent
- Adult patients ≥ 18 years
- Histologically or cytologically confirmed diagnosis of limited or extensive stage SCLC which failed one prior platinum-containing regimen and with a chemotherapy-free interval (CTFI, time from the last dose of first-line chemotherapy to the occurrence of progressive disease) ≥ 30 days. Small-cell carcinoma of unknown primary site with or without neuroendocrine features confirmed in histology test(s) performed on metastatic lesion(s) are eligible, if Ki-67/MIB-1 is expressed in >50% of tumor cells.
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) ≤ 2.
- Adequate hematological, renal, metabolic and hepatic function within 7-10 days prior to randomization
- At least three weeks since last prior anticancer treatment and adequate recovery from prior treatment toxicity
- Prior radiotherapy (RT): At least four weeks since completion of whole-brain irradiation, at least two weeks since completion of prophylactic cranial irradiation, and to any other site.
- Evidence of non-childbearing status for women of childbearing potential (WOCBP). WOCBP must agree to use a highly effective contraceptive measure up to six weeks after treatment discontinuation. Fertile male patients with WOCBP partners should use condoms during treatment and for four months following the last investigational medicinal product dose.-

Critères de non-inclusion : - More than one prior chemotherapy-containing line(re-challenge with the same initial regimen is not allowed)
- Patients who never received platinum-containing regimen for Small-cell Lung Cancer (SCLC)
- Prior treatment with PM01183, topotecan or anthracyclines.
- Limited-stage patients who are candidates for local or regional therapy
- Impending need for palliative RT or surgery for pathological fractures and/or for medullary compression within four weeks prior to randomization.
- Symptomatic or progressing or steroid requiring Central Nervous System (CNS) involvement disease at least four weeks prior to randomization
- Concomitant diseases/conditions:
Angina, myocardial infarction, congestive heart failure or clinically significant valvular heart disease, arrhythmia, immunodeficiency (including known HIV seropositive), ongoing or treatment-requiring chronic liver disease, active infection, oxygen requirement within two weeks prior to randomization, diffuse interstitial lung disease (ILD) or pulmonary fibrosis, second invasive malignancy treated with chemotherapy and/or radiotherapy, invasive fungal infections requiring systemic treatment within 12 weeks of randomization.
- Pregnant or breast feeding women
NCT
Promoteur
Coordonnateur
Informations relatives au promoteur
NCT :
Promoteur :
PHARMA MAR
Type de sponsor : Industriel
PHARMA MAR - PHARMA MAR
00000 HORS FRANCE

Coordonnateur :
Centre investigateur
Investigateur
TEC / ARC / IDE
État
MÀJ
Informations relatives aux investigateurs
Centre investigateur :
Centre François BACLESSE - 3 avenue du Général Harris - 14000 CAEN

Investigateur :
Radj GERVAIS

TEC / ARC / IDE :
Karim HAMOND
k.hamond@
baclesse.unicancer.fr

Ouverture de l'essai : CLOS

MAJ : 24/08/2018