The purpose of this study is to evaluate the outcome (survival) of Adult T-cell leukemia / lymphoma (ATL) patients who receive or not specific treatment for their hemopathy (cohort 1) and the outcome (survival) of HTLV-1 chronically infected patients with / without extra-haematological disorders (cohort 2).
Study Type
OBSERVATIONAL
Enrollment
120
Hôpital Necker Enfants Malades
Paris, France
Number of survivors
for cohorts 1 and 2
Time frame: Up to 1 year
Number of survivors at 2 years
for cohorts 1 and 2
Time frame: At 2 years
Number of survivors at 5 years
for cohorts 1 and 2
Time frame: 5 years
HTLV-1 proviral load
for cohorts 1 and 2
Time frame: day 1
viral integration profile
for cohorts 1 and 2
Time frame: day 1
lymphocyte phenotyping of tumor cells
for cohorts 1 and 2
Time frame: day 1
genetic analysis of tumor cells by Next-generation sequencing (NGS)
for cohorts 1 and 2
Time frame: day 1
number of patients with HTLV-1-related hematological disorders
for cohort 1
Time frame: day 1
number of patients with HTLV-1-related extra-hematological disorders
for cohort 1
Time frame: day 1
types of ATL
According the Shimoyama classification (smoldering, chronic, Acute and Lymphoma) for cohort 1
Time frame: day 1
Treatment lines
Chemotherapy type, number of Chemotherapy cycles, efficacity of Chemotherapy : Number of complete remissions following treatment : for cohort 1
Time frame: during 5 years
Response to induction therapy
according to established response criteria for ATL for cohort 1
Time frame: during 5 years
Progression free survival (PFS)
for cohort 1
Time frame: during 5 years
relapse-related mortality
for cohort 1
Time frame: during 5 years
chemotherapy-related mortality
for cohort 1
Time frame: during 5 years
transplant-related mortality
for cohort 1
Time frame: during 5 years
Number of serious adverse events according to WHO classification related to treatment received
for cohort 1
Time frame: during 5 years
Allograft-specific characteristic
(donor type, conditioning type, engraftment, graft-related mortality) for cohort 1
Time frame: during 5 years
number of progression to ATL
Time frame: at 2 years
Number of progression to ATL
Time frame: At 5 years
number of patients with HTLV-1-related extrahematological disorders
Time frame: during 5 years
Number of patients with corticotherapy for extrahematological complications
Dose of corticotherapy for extrahematological complications, number of days with corticotherapy for extrahematological complications
Time frame: during 5 years
Number of Serious adverse events according to WHO classification related to treatment received
Time frame: during 5 years
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