Evidence map›Paper›PMID 39634261›Full record

SynthesisFrontiers in oncology2024

Ponatinib vs. asciminib in post-second-generation tyrosine kinase inhibitor therapy for chronic-phase chronic myeloid leukemia: a matching-adjusted indirect comparison.

Valentin Garcia-Gutierrez, Fei Huang, Ajibade Ashaye, Mehul Dalal, Victor Laliman-Khara, Massimo Breccia, Megan Rutherford, Hoora Moradian, Petros Patos, Elias Joseph Jabbour

4 registry-linked trialsAbstract readSystematic Review
In one paragraph

Synthesis in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01207440 phase2completednot on this map

A Pivotal Phase 2 Trial of Ponatinib (AP24534) in Patients With Refractory Chronic Myeloid Leukemia and Ph+ Acute Lymphoblastic Leukemia

TypeinterventionalSponsorAriad PharmaceuticalsRan2010 to 2019Enrolled449ConditionsChronic Myeloid Leukemia, Ph+ Acute Lymphoblastic LeukemiaArmsPonatinib
NCT02081378 phase1completednot on this map

A Phase I, Multicenter, Open-label Study of Oral ABL001 in Patients With Chronic Myelogenous Leukemia (CML) or Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia (Ph+ ALL)

TypeinterventionalSponsorNovartis PharmaceuticalsRan2014 to 2023Enrolled326ConditionsChronic Myelogenous Leukemia, Philadelphia Chromosome-positive Acute Lymphoblastic LeukemiaArmsAsciminib (ABL001), Nilotinib, Imatinib, Dasatinib
NCT02467270 phase2completednot on this map

A Randomized, Open-label, Phase 2 Trial of Ponatinib in Patients With Resistant Chronic Phase Chronic Myeloid Leukemia to Characterize the Efficacy and Safety of a Range of Doses

TypeinterventionalSponsorTakedaRan2015 to 2025Enrolled283ConditionsMyeloid Leukemia, Chronic, Chronic PhaseArmsPonatinib
NCT03106779 phase3completednot on this map

A Phase 3, Multi-center, Open-label, Randomized Study of Oral ABL001 Versus Bosutinib in Patients With Chronic Myelogenous Leukemia in Chronic Phase (CML-CP), Previously Treated With 2 or More Tyrosine Kinase Inhibitors

TypeinterventionalSponsorNovartis PharmaceuticalsRan2017 to 2024Enrolled233ConditionsChronic Myelogenous LeukemiaArmsAsciminib, Bosutinib
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Valentin Garcia-GutierrezRamón y Cajal University Hospital, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Universidad de Alcalá, Madrid, Spain.
Fei HuangGlobal Evidence and Outcomes Oncology, Takeda Development Center Americas, Inc, Lexington, MA, United States.
Ajibade AshayeGlobal Evidence and Outcomes Oncology, Takeda Development Center Americas, Inc, Lexington, MA, United States.
Mehul DalalGlobal Evidence and Outcomes Oncology, Takeda Development Center Americas, Inc, Lexington, MA, United States.
Victor Laliman-KharaAdvanced Analytics Advisory, HEOR, Cytel Inc., Waltham, MA, United States.
Massimo BrecciaDepartment of Translational and Precision Medicine, Sapienza University, Rome, Italy.
Megan RutherfordAdvanced Analytics Advisory, HEOR, Cytel Inc., Waltham, MA, United States.
Hoora MoradianComparative Effectiveness, Cytel Inc., Waltham, MA, United States.
Petros PatosHematology, Region Europe, Incyte Biosciences International Sàrl, Morges, Switzerland.
Elias Joseph JabbourDepartment of Leukemia, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ponatinib and asciminib are approved for third-line therapy in chronic-phase chronic myeloid leukemia (CP-CML) and are the only drugs approved for patients with the T315I mutation in the United States. In Europe, only ponatinib is approved for patients with the T315I mutation. Methods: Clinical trials evaluating ponatinib or asciminib in patients with relapsed and refractory (R/R) CP-CML who failed one or more second-generation TKIs or had the T315I mutation were identified in a systematic review of medical literature databases. A matching-adjusted indirect comparison (MAIC) analysis with individual patient-level data with ponatinib was used to balance baseline characteristics between ponatinib and asciminib groups. After matching, the response rate was calculated using the MAIC weight for each patient and the difference in response rate was calculated using a two-independent proportion Z-test. Cumulative rates of Results: The MAIC included four trials (ponatinib: NCT02467270, NCT01207440; asciminib: NCT02081378, NCT03106779). In patients without baseline response of Conclusion: After key baseline characteristics adjustment, cumulative

Indexed as

asciminibBCR::ABL1 (BCR-ABL1)chronic myeloid leukemiamajor molecular responseponatinibT315I mutation

Identifiers

PMID39634261
PMCPMC11615674

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.