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Association details:
Evidence:
Evidence Level:
Sensitive: A1 - Approval
Published date:
09/18/2014
Excerpt:
Zydelig is indicated in combination with an anti‑CD20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (CLL)...as first line treatment in the presence of 17p deletion or TP53 mutation in patients who are not eligible for any other therapies.
Evidence Level:
Sensitive: A2 - Guideline
New
Source:
Title:

Chronic lymphocytic leukaemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

Excerpt:
Recommendations: TP53 mutation or del(17p): ibrutinib or acalabrutinib or venetoclax plus obinutuzumab or venetoclax alone or idelalisib plus rituximab [III, A].
DOI:
10.1016/j.annonc.2020.09.019
Evidence Level:
Sensitive: A2 - Guideline
New
Source:
Excerpt:
Suggested treatment regimens...CLL/SLL with del(17p)/TP53 mutation…Relapsed/refractory therapy…preferred regimen…idelalisib + rituximab
Evidence Level:
Sensitive: B - Late Trials
New
Title:

Idelalisib or placebo in combination with bendamustine and rituximab in patients with relapsed or refractory chronic lymphocytic leukaemia: interim results from a phase 3, randomised, double-blind, placebo-controlled trial

Excerpt:
Randomisation was stratified by high-risk features (IGHV, del[17p], or TP53 mutation)... Idelalisib in combination with bendamustine plus rituximab improved progression-free survival compared with bendamustine plus rituximab alone in patients with relapsed or refractory chronic lymphocytic leukaemia.
Secondary therapy:
bendamustine
DOI:
10.1016/S1470-2045(16)30671-4
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Title:

Idelalisib (PI3Kδ inhibitor) therapy for patients with relapsed/refractory chronic lymphocytic leukemia: A Swedish nation-wide real-world report on consecutively identified patients

Published date:
07/27/2023
Excerpt:
Thirty-seven patients with relapsed/refractory disease were included. The median number of prior lines of therapy was 3 (range 1-11); the median age was 69 years (range 50-89); 22% had Cumulative Illness Rating Scale (CIRS) >6 and 51% had del(17p)/TP53 mutation. The overall response rate was 65% (all but one was partial response [PR]). The median duration of therapy was 9.8 months (range 0.9-44.8). The median progression-free survival was 16.4 months (95% CI: 10.4-26.3)...Our real-world results suggest that idelalisib is an effective and relatively safe treatment for patients with advanced-stage CLL when no other therapies exist.
DOI:
10.1111/ejh.14065