Next‐generation sequencing improves BCR‐ABL1 mutation detection in Philadelphia chromosome‐positive acute lymphoblastic leukaemia. (6th January 2021)

• Record Type: Journal Article
• Authors: Soverini, Simona; Martelli, Margherita; Bavaro, Luana; De Benedittis, Caterina; Papayannidis, Cristina; Sartor, Chiara; Sorà, Federica; Albano, Francesco; Galimberti, Sara; Abruzzese, Elisabetta; Annunziata, Mario; Russo, Sabina; Stulle, Manuela; Imovilli, Annalisa; Bonifacio, Massimiliano; Maino, Elena; Stagno, Fabio; Maria Basilico, Claudia; Borlenghi, Erika; Fozza, Claudio; Mignone, Flavio; Minari, Roberta; Stella, Stefania; Baccarani, Michele; Cavo, Michele; Martinelli, Giovanni
• Is Part Of: British journal of haematology. Volume 193:Number 2(2021)
• Page Start: 271
• Page End: 279
• Publication Date: 2021-01-06
• Subjects: acute lymphoblastic leukemia -- BCR‐ABL1 -- mutations -- tyrosine kinase inhibitors -- NGS; Hematology -- Periodicals; Blood -- Diseases -- Periodicals; 616.15
• DOI: 10.1111/bjh.17301
• Languages: English
• ISSNs: 0007-1048

Abstract

Summary: BCR‐ABL1 kinase domain mutation testing in tyrosine kinase inhibitor (TKI)‐resistant Philadelphia chromosome‐positive (Ph+) acute lymphoblastic leukaemia (ALL) patients is routinely performed by Sanger sequencing (SS). Recently, next‐generation sequencing (NGS)‐based approaches have been developed that afford greater sensitivity and straightforward discrimination between compound and polyclonal mutations. We performed a study to compare the results of SS and NGS in a consecutive cohort of 171 Ph+ ALL patients. At diagnosis, 0/44 and 3/44 patients were positive for mutations by SS and NGS respectively. Out of 47 patients with haematologic resistance, 45 had mutations according to both methods, but in 25 patients NGS revealed additional mutations undetectable by SS. Out of 80 patients in complete haematologic response but with BCR‐ABL1 ≥0·1%, 28 (35%) and 52 (65%) were positive by SS and NGS respectively. Moreover, in 12 patients positive by SS, NGS detected additional mutations. NGS resolved clonal complexity in 34 patients with multiple mutations at the same or different codons and identified 35 compound mutations. Our study demonstrates that, in Ph+ ALL on TKI therapy, NGS enables more accurate assessment of mutation status both in patients who fail therapy and in patients with minimal residual disease above 0·1%.