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TEST:
clonoSEQ

Type:
FDA Approved
Evidence Level:
Sensitive: B - Late Trials

[TP53 mutation-Chronic Lymphocytic Leukemia-venetoclax + obinutuzumab]

Source:
Title:
GENETIC MARKERS AND OUTCOME IN FRONT LINE OBINUTUZUMAB PLUS CHLORAMBUCIL OR VENETOCLAX - UPDATED ANALYSIS OF THE CLL14 TRIAL
Published date:
05/12/2021
Excerpt:
CONTRADICTED EVIDENCE:...gene mutations in the CLL14 trial comparing obinutuzumab+chlorambucil (GClb) vs. obinutuzumab+venetoclax (VenG) in 432 patients...Overall survival (OS) was shorter with del(17p) and TP53 mutation in both treatment arms (GClb: HR 5.7 and HR 3.1, VenG: HR 3.5 and HR 3.0, all p<0.01)...
Trial ID:
Evidence Level:
Sensitive: B - Late Trials

[Chr del(17p)-Chronic Lymphocytic Leukemia-venetoclax + obinutuzumab]

Source:
Title:
GENETIC MARKERS AND OUTCOME IN FRONT LINE OBINUTUZUMAB PLUS CHLORAMBUCIL OR VENETOCLAX - UPDATED ANALYSIS OF THE CLL14 TRIAL
Published date:
05/12/2021
Excerpt:
CONTRADICTING EVIDENCE:…gene mutations in the CLL14 trial comparing obinutuzumab+chlorambucil (GClb) vs. obinutuzumab+venetoclax (VenG) in 432 patients (1:1) with CIRS>6 and/or creatinine clearance < 70 ml/min….Overall survival (OS) was shorter with del(17p) and TP53 mutation in both treatment arms (GClb: HR 5.7 and HR 3.1, VenG: HR 3.5 and HR 3.0, all p<0.01)…
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials

[BCR-ABL1 fusion-Acute Lymphocytic Leukemia-ponatinib + blinatumomab]

Source:
Title:
A Phase II Study of the Sequential Combination of Low-Intensity Chemotherapy (mini-hyper-CVD) and Ponatinib Followed By Blinatumomab and Ponatinib in Patients with Philadelphia Chromosome-Positive (Ph+) Acute Lymphoblastic Leukemia (ALL)Clinically Relevant Abstract
Published date:
11/15/2022
Excerpt:
With a median follow-up of 23 months (range, 6-31), the 2-year CRD and OS rates are 90% and 78%, respectively, across all cohorts (Figure 1), and are 89% and 82%, respectively in the ND cohort...Sequential combination of low-intensity chemotherapy and ponatinib followed by blinatumomab and ponatinib is highly effective and well tolerated in Ph+ ALL.
Secondary therapy:
Chemotherapy
DOI:
https://doi.org/10.1182/blood-2022-167883
Evidence Level:
Sensitive: C3 – Early Trials

[TP53 mutation-Chronic Lymphocytic Leukemia-venetoclax + obinutuzumab + acalabrutinib]

Source:
Title:
344 Updated Results from a Multicenter, Phase 2 Study of Acalabrutinib, Venetoclax, Obinutuzumab (AVO) in a Population of Previously Untreated Patients with CLL Enriched for High-Risk Disease
Published date:
11/03/2022
Excerpt:
In the 29 pts with TP53-aberrant disease evaluable at C16D1, the best ORR is 100% (52% CR, 48% PR)...AVO is a highly active, well-tolerated triplet in a frontline CLL population enriched for high-risk disease, with 83% of TP53-aberrant pts achieving BM-uMRD after 15 mos of tx.
DOI:
https://doi.org/10.1182/blood-2022-168003
Trial ID: