Table 3.

PD and subsequent treatment

PatGenetics baselineC15 remissionMRD at C15EOT datePFS dateTime point of PD in mo, from registration datePeriod of subsequent therapyName of the first subsequent therapy
Del(17p) 88%
TP53mut
Exon 8 60% 
CR uMRD February 2018 September 2019 32.0   
Del(17p) 21.5%
TP53mut
Exon 8 20% 
CR uMRD November 2017 February 2019 27.2   
3  Del(17p) 85%
TP53mut
Exon 5 60% 
CR uMRD December 2017 September 2019 33.5 From November 2018 to February 2019 Obinutuzumab 
Del(17p) 93.5%
TP53mut
Exon 8 70% 
CR uMRD May 2018 December 2019 32.1 February 2020 Acalabrutinib/obinutuzumab/venetoclax 
Del(17p) 93%
TP53 umut 
PR uMRD PB; no BM November 2018 September 2019 24.6 February 2020 Acalabrutinib/obinutuzumab/venetoclax 
6  Del(17p) 93.5%
TP53mut
Exon 7 95% 
PR uMRD December 2018 January 2020 24.2 from April 2020 to July 2020 Venetoclax 
Del(17p) 16.5%
TP53mut
Exon 6 70% 
CR uMRD PB; iMRD BM April 2019 June 2021 38.6   
PatGenetics baselineC15 remissionMRD at C15EOT datePFS dateTime point of PD in mo, from registration datePeriod of subsequent therapyName of the first subsequent therapy
Del(17p) 88%
TP53mut
Exon 8 60% 
CR uMRD February 2018 September 2019 32.0   
Del(17p) 21.5%
TP53mut
Exon 8 20% 
CR uMRD November 2017 February 2019 27.2   
3  Del(17p) 85%
TP53mut
Exon 5 60% 
CR uMRD December 2017 September 2019 33.5 From November 2018 to February 2019 Obinutuzumab 
Del(17p) 93.5%
TP53mut
Exon 8 70% 
CR uMRD May 2018 December 2019 32.1 February 2020 Acalabrutinib/obinutuzumab/venetoclax 
Del(17p) 93%
TP53 umut 
PR uMRD PB; no BM November 2018 September 2019 24.6 February 2020 Acalabrutinib/obinutuzumab/venetoclax 
6  Del(17p) 93.5%
TP53mut
Exon 7 95% 
PR uMRD December 2018 January 2020 24.2 from April 2020 to July 2020 Venetoclax 
Del(17p) 16.5%
TP53mut
Exon 6 70% 
CR uMRD PB; iMRD BM April 2019 June 2021 38.6   

TP53mut, TP53 mutation; umut, unmutated. Pat, patient; del, deletion; mut, mutated; umut, unmutated; C, cycle; CR, complete remission; PR, partial remission; uMRD, undectable minimal residual disease; iMRD, intermediate minimal residual disease; PB, peripheral blood; EOT, end of treatment; PFS, progression-free survival.

A Richter transformation (other: diffuse large B-cell lymphoma clonal relationship not analyzed) has been documented 12 months after EOT in May 2020, after treatment with venetoclax, rituximab/idelalisib, and ibrutinib monotherapy was administered.

Due to detectable MRD in November 2018, the patient receieved obinutuzmab. The patient had a disease progression in September 2019.

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