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Assessment of the Efficacy of Therapies Following Venetoclax Discontinuation in CLL Reveals BTK Inhibition as an Effective Strategy.


ABSTRACT:

Purpose

Venetoclax-based therapy is a standard-of-care option in first-line and relapsed/refractory chronic lymphocytic leukemia (CLL). Patient management following venetoclax discontinuation remains nonstandard and poorly understood.

Experimental design

To address this, we conducted a large international study to identify a cohort of 326 patients who discontinued venetoclax and have been subsequently treated. Coprimary endpoints were overall response rate (ORR) and progression-free survival for the post-venetoclax treatments stratified by treatment type [Bruton's tyrosine kinase inhibitor (BTKi), PI3K inhibitor (PI3Ki), and cellular therapies].

Results

We identified patients with CLL who discontinued venetoclax in the first-line (4%) and relapsed/refractory settings (96%). Patients received a median of three therapies prior to venetoclax; 40% were BTKi naïve (n = 130), and 81% were idelalisib naïve (n = 263). ORR to BTKi was 84% (n = 44) in BTKi-naïve patients versus 54% (n = 30) in BTKi-exposed patients. We demonstrate therapy selection following venetoclax requires prior novel agent exposure consideration and discontinuation reasons.

Conclusions

For BTKi-naïve patients, selection of covalently binding BTKis results in high ORR and durable remissions. For BTKi-exposed patients, covalent BTK inhibition is not effective in the setting of BTKi resistance. PI3Kis following venetoclax do not appear to result in durable remissions. We conclude that BTKi in naïve or previously responsive patients and cellular therapies following venetoclax may be the most effective strategies.See related commentary by Rogers, p. 3501.

SUBMITTER: Mato AR 

PROVIDER: S-EPMC8588795 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Assessment of the Efficacy of Therapies Following Venetoclax Discontinuation in CLL Reveals BTK Inhibition as an Effective Strategy.

Mato Anthony R AR   Roeker Lindsey E LE   Jacobs Ryan R   Hill Brian T BT   Lamanna Nicole N   Brander Danielle D   Shadman Mazyar M   Ujjani Chaitra S CS   Yazdy Maryam Sarraf MS   Perini Guilherme Fleury GF   Pinilla-Ibarz Javier A JA   Barrientos Jacqueline J   Skarbnik Alan P AP   Torka Pallawi P   Pu Jeffrey J JJ   Pagel John M JM   Gohil Satyen S   Fakhri Bita B   Choi Michael M   Coombs Catherine C CC   Rhodes Joanna J   Barr Paul M PM   Portell Craig A CA   Parry Helen H   Garcia Christine A CA   Whitaker Kate J KJ   Winter Allison M AM   Sitlinger Andrea A   Khajavian Sirin S   Grajales-Cruz Ariel F AF   Isaac Krista M KM   Shah Pratik P   Akhtar Othman S OS   Pocock Rachael R   Lam Kentson K   Voorhees Timothy J TJ   Schuster Stephen J SJ   Rodgers Thomas D TD   Fox Christopher P CP   Martinez-Calle Nicolas N   Munir Talha T   Bhavsar Erica B EB   Bailey Neil N   Lee Jason C JC   Weissbrot Hanna B HB   Nabhan Chadi C   Goodfriend Julie M JM   King Amber C AC   Zelenetz Andrew D AD   Dorsey Colleen C   Bigelow Kayla K   Cheson Bruce D BD   Allan John N JN   Eyre Toby A TA  

Clinical cancer research : an official journal of the American Association for Cancer Research 20200320 14


<h4>Purpose</h4>Venetoclax-based therapy is a standard-of-care option in first-line and relapsed/refractory chronic lymphocytic leukemia (CLL). Patient management following venetoclax discontinuation remains nonstandard and poorly understood.<h4>Experimental design</h4>To address this, we conducted a large international study to identify a cohort of 326 patients who discontinued venetoclax and have been subsequently treated. Coprimary endpoints were overall response rate (ORR) and progression-fr  ...[more]

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