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ItaliaN Observational Study of Patients With Acute Lymphoblastic Leukemia Treated With Anti-CD22 Immunoconjugate

Conditions
Acute Lymphoblastic Leukemia
Registration Number
NCT03898128
Lead Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
Brief Summary

In phase 2 and phase 3 studies, inotuzumab has shown evidence of single agent anti-leukemic activity and proved to be particularly effective in providing a deep response, with an acceptable safety profile. Since 2014 anti-CD22 has been available for compassionate use in Italy.

In this non-interventional retrospective study, toxicity, effectiveness and costs assessment data will be collected from patients with ALL, to improve the knowledge about anti-CD22 treatment in clinical practice. Collecting data of patients and analyzing a large unbiased patient-set of patients receiving anti-CD22 immunoconjugates could enlarge our knowledge on therapies engaging CD22

Detailed Description

In phase 2 and phase 3 studies, inotuzumab has shown evidence of single agent anti-leukemic activity and proved to be particularly effective in providing a deep response, with an acceptable safety profile. Since 2014 anti-CD22 has been available for compassionate use in Italy.

In this non-interventional retrospective study, toxicity, effectiveness and costs assessment data will be collected from patients with ALL, to improve the knowledge about anti-CD22 treatment in clinical practice.

Despite recent advancements in the treatment of hematological malignancies, still a considerable number of cases cannot be cured and represent real societal challenges with a relevant social and economic impact. Indeed, treatments are becoming more expensive and the current state of the art does not allow a good prediction of the therapeutic outcome. In particular, several steps of the diagnostic and therapeutic paths should be improved, from early and advanced diagnosis, in order to avoid treatment delays or impairment, to prognostic assessment and monitoring of therapeutic response. The unsatisfactory response to conventional chemotherapy has led to the development of high-cost targeted therapies, whose administration and schedules has to be guided by defined molecular criteria. Beside the economic perspective, these novel drugs have relevant side effects that cannot be predicted before treatment starts.

The management of hematological malignancies is further complicated by the high level of disease heterogeneity in terms of pathogenetic and molecular mechanisms. A number of subtypes have been defined for each disease, based on cytogenetic and molecular profiles and relevant differences can be even observed within the same disease subtype, leading to different clinical outcomes and responses to treatment and to guide therapeutic decisions for patients affected by CD22 positive ALL.

Due to the observational nature of the study, for the patient there is no benefit expected. For this observational nature of the study, for the patient there is no risk about his health. Data will be treated according GCP/EU laws/Italian laws/local laws according the most restrictive between these laws.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  1. Patient with ALL according WHO 2016 classification.
  2. Patient who received any anti-CD22 immunoconjugate from 2014 to 01-Mar-2019 outside clinical trials.
Exclusion Criteria
  1. Patients who received anti-CD22 treatment within a clinical trial

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of Adverse Events of grade 3 and 4up to 12 months

toxicity profile of the therapy with antiCD22 immunoconjugates in patients with ALL

Secondary Outcome Measures
NameTimeMethod
Overall survivalup to 18 months

Overall Survival (OS), defined as the number of days between the first study drug administration and death from any cause

Disease free survivalup to 18 months

Disease Free Survival (DFS), defined as the number of days between the first study drug administration and any event including disease progression or death from any cause

Response to therapyup to 18 months

response to therapy (CR, CRi, MRD and bridge to transplant)

Trial Locations

Locations (5)

AUSL Romagna

🇮🇹

Ravenna, RA, Italy

Irst Irccs

🇮🇹

Meldola (FC), FC, Italy

Azienda ULSS2 Marca Trevigiana

🇮🇹

Treviso, TV, Italy

Ospedale S. Eugenio

🇮🇹

Roma, Italy

ULSS 3 Serenissima

🇮🇹

Mestre, Venezia, Italy

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