Matching-adjusted indirect comparison of asciminib versus other treatments in chronic-phase chronic myeloid leukemia after failure of two prior tyrosine kinase inhibitors.


Journal

Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 08 11 2022
accepted: 26 12 2022
medline: 24 7 2023
pubmed: 28 1 2023
entrez: 27 1 2023
Statut: ppublish

Résumé

The current standard of care for chronic-phase chronic myeloid leukemia (CP-CML) is tyrosine kinase inhibitors (TKIs). Treatment recommendations are unclear for CP-CML failing ≥ 2 lines of treatment, partly due to the paucity of head-to-head trials evaluating TKIs. Thus, matching-adjusted indirect comparisons (MAICs) were conducted to compare asciminib with competing TKIs in third- or later line (≥ 3L) CP-CML. Individual patient-level data for asciminib (ASCEMBL; follow-up: ≥ 48 weeks) and published aggregate data for comparator TKIs (ponatinib, nilotinib, and dasatinib) informed the analyses. Major molecular response (MMR), complete cytogenetic response (CCyR), and time to treatment discontinuation (TTD) were assessed, where feasible. Asciminib was associated with statistically significant improvements in MMR by 6 (relative risk [RR]: 1.55; 95% confidence interval [CI]: 1.02, 2.36) and 12 months (RR: 1.48; 95% CI: 1.03, 2.14) vs ponatinib. For CCyR, the results vs ponatinib were similar by 6 (RR: 1.11; 95% CI: 0.81, 1.52) and 12 months (RR: 0.97; 95% CI: 0.73, 1.28). Asciminib was associated with improvements in MMR by 6 months vs dasatinib but with a CI overlapping one (RR 1.52; 95% CI: 0.66, 3.53). Asciminib was associated with statistically significant improvements in CCyR by 6 (RR: 3.57; 95% CI: 1.42, 8.98) and 12 months (RR: 2.03; 95% CI: 1.12, 3.67) vs nilotinib/dasatinib. Median TTD was unreached for asciminib in ASCEMBL. However, post-adjustment asciminib implied prolonged TTD vs nilotinib and dasatinib, but not vs ponatinib. These analyses demonstrate favorable outcomes with asciminib versus competing TKIs, highlighting its therapeutic potential in ≥ 3L CP-CML.

Identifiants

pubmed: 36707445
doi: 10.1007/s00432-022-04562-5
pii: 10.1007/s00432-022-04562-5
pmc: PMC10356870
doi:

Substances chimiques

Dasatinib RBZ1571X5H
Antineoplastic Agents 0
asciminib 0
Tyrosine Kinase Inhibitors 0
Protein Kinase Inhibitors 0
Pyrimidines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6247-6262

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© 2023. The Author(s).

Références

Blood. 2021 Nov 25;138(21):2031-2041
pubmed: 34407542
Hematology Am Soc Hematol Educ Program. 2021 Dec 10;2021(1):113-121
pubmed: 34889360
Lancet. 2007 Jul 28;370(9584):342-50
pubmed: 17662883
Value Health. 2012 Sep-Oct;15(6):940-7
pubmed: 22999145
Nature. 2017 Mar 30;543(7647):733-737
pubmed: 28329763
Haematologica. 2013 Mar;98(3):399-403
pubmed: 22801965
Blood. 1993 Aug 1;82(3):691-703
pubmed: 8338938
Med Decis Making. 2018 Feb;38(2):200-211
pubmed: 28823204
J Clin Oncol. 2016 Aug 20;34(24):2851-7
pubmed: 27325849
Leukemia. 2021 Feb;35(2):440-453
pubmed: 33414482
Leukemia. 2016 May;30(5):1044-54
pubmed: 26837842
Pharm Stat. 2022 Sep;21(5):974-987
pubmed: 35343622
Leuk Res. 2020 Nov;98:106458
pubmed: 33096322
Leukemia. 2020 Apr;34(4):966-984
pubmed: 32127639
Curr Med Res Opin. 2019 Mar;35(3):479-487
pubmed: 30086654
Ann Oncol. 2017 Jul 1;28(suppl_4):iv41-iv51
pubmed: 28881915
Leukemia. 2020 Jun;34(6):1495-1502
pubmed: 32366938
Clinics (Sao Paulo). 2015 Aug;70(8):550-5
pubmed: 26247667
Front Oncol. 2019 Jul 03;9:603
pubmed: 31334123
Blood. 2010 Dec 16;116(25):5497-500
pubmed: 20833982
Med Decis Making. 2013 Jul;33(5):607-17
pubmed: 23104435
Blood. 2009 Nov 12;114(20):4361-8
pubmed: 19729517
Leukemia. 2010 Jul;24(7):1299-301
pubmed: 20520639
Int J Technol Assess Health Care. 2019 Jan;35(3):221-228
pubmed: 31190671
Lancet Haematol. 2015 May;2(5):e186-93
pubmed: 26688093
Am J Hematol. 2020 Jun;95(6):691-709
pubmed: 32239758
Leuk Lymphoma. 2018 Jun;59(6):1312-1322
pubmed: 28972430
Acta Haematol. 2019;142(2):79-86
pubmed: 31096222
J Hematol Oncol. 2021 Mar 18;14(1):44
pubmed: 33736651
J Clin Oncol. 2016 Jul 10;34(20):2333-40
pubmed: 27217448
Cell Cycle. 2011 Jan 15;10(2):250-60
pubmed: 21220945
Pharmacoeconomics. 2010;28(10):935-45
pubmed: 20831302
Am J Hematol. 2016 Feb;91(2):252-65
pubmed: 26799612

Auteurs

Ehab Atallah (E)

Medical College of Wisconsin, Milwaukee, WI, USA. eatallah@mcw.edu.

Michael J Mauro (MJ)

Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Andreas Hochhaus (A)

Universitätsklinikum Jena, Jena, Germany.

Carla Boquimpani (C)

HEMORIO, State Institute of Hematology Arthur de Siquiera Cavalcanti, Rio de Janeiro, Brazil.
Oncoclínica Centro de Tratamento Oncológico, Rio de Janeiro, Brazil.

Yosuke Minami (Y)

National Cancer Center Hospital East, Kashiwa, Japan.

Vikalp Kumar Maheshwari (VK)

Novartis Healthcare Pvt. Ltd, Hyderabad, India.

Lovneet Saini (L)

Novartis Healthcare Pvt. Ltd, Hyderabad, India.

Regina Corbin (R)

Novartis Services Inc., East Hanover, NJ, USA.

Delphine Réa (D)

Adult Hematology Hôpital Saint-Louis and FiLMC, Paris, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH