Craig S Boddy1, Shuo Ma2. 1. Division of Hematology/Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, 303 E Superior Street, Lurie 3-103, Chicago, IL, 60611, USA. 2. Division of Hematology/Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, 676 N St. Clair Street, Suite 850, Chicago, IL, 60611, USA. shuo-ma@northwestern.edu.
Abstract
PURPOSE OF REVIEW: Chronic lymphocytic leukemia (CLL) has multiple current frontline therapy options, including chemoimmunotherapy (CIT) and most recently, ibrutinib. Here, we review the most recent updates in the frontline treatment of CLL, including updates in CIT, updates in targeted therapies, and ongoing clinical trials. RECENT FINDINGS: Ibrutinib was FDA-approved for the upfront treatment of CLL in 2016 after being studied in older patients and those with 17p deletions or TP53 mutations. The introduction of ibrutinib has dramatically changed the treatment paradigm of CLL. Recent updates in CIT include that immunoglobulin heavy chain variable (IGHV) gene mutation status is strongly predictive of response to CIT. Regarding targeted therapy, next-generation BTK and PI3K inhibitors are currently being studied in the upfront treatment of CLL, which may have less toxicity than their first-generation counterparts. Other novel targeted therapies are being studied in the frontline setting, most notably venetoclax including in combinations, with hopes to achieve chemotherapy-free, time-limited treatment options. Multiple key ongoing phase 3 clinical trials will be answering these important clinical questions.
PURPOSE OF REVIEW: Chronic lymphocytic leukemia (CLL) has multiple current frontline therapy options, including chemoimmunotherapy (CIT) and most recently, ibrutinib. Here, we review the most recent updates in the frontline treatment of CLL, including updates in CIT, updates in targeted therapies, and ongoing clinical trials. RECENT FINDINGS:Ibrutinib was FDA-approved for the upfront treatment of CLL in 2016 after being studied in older patients and those with 17p deletions or TP53 mutations. The introduction of ibrutinib has dramatically changed the treatment paradigm of CLL. Recent updates in CIT include that immunoglobulin heavy chain variable (IGHV) gene mutation status is strongly predictive of response to CIT. Regarding targeted therapy, next-generation BTK and PI3K inhibitors are currently being studied in the upfront treatment of CLL, which may have less toxicity than their first-generation counterparts. Other novel targeted therapies are being studied in the frontline setting, most notably venetoclax including in combinations, with hopes to achieve chemotherapy-free, time-limited treatment options. Multiple key ongoing phase 3 clinical trials will be answering these important clinical questions.
Authors: Kirsten Fischer; Jasmin Bahlo; Anna Maria Fink; Valentin Goede; Carmen Diana Herling; Paula Cramer; Petra Langerbeins; Julia von Tresckow; Anja Engelke; Christian Maurer; Gabor Kovacs; Marco Herling; Eugen Tausch; Karl-Anton Kreuzer; Barbara Eichhorst; Sebastian Böttcher; John F Seymour; Paolo Ghia; Paula Marlton; Michael Kneba; Clemens-Martin Wendtner; Hartmut Döhner; Stephan Stilgenbauer; Michael Hallek Journal: Blood Date: 2015-10-20 Impact factor: 22.113
Authors: Susan O'Brien; Jeffrey A Jones; Steven E Coutre; Anthony R Mato; Peter Hillmen; Constantine Tam; Anders Österborg; Tanya Siddiqi; Michael J Thirman; Richard R Furman; Osman Ilhan; Michael J Keating; Timothy G Call; Jennifer R Brown; Michelle Stevens-Brogan; Yunfeng Li; Fong Clow; Danelle F James; Alvina D Chu; Michael Hallek; Stephan Stilgenbauer Journal: Lancet Oncol Date: 2016-09-13 Impact factor: 41.316
Authors: Kirsten Fischer; Othman Al-Sawaf; Anna-Maria Fink; Mark Dixon; Jasmin Bahlo; Simon Warburton; Thomas J Kipps; Robert Weinkove; Sue Robinson; Till Seiler; Stephen Opat; Carolyn Owen; Javier López; Kathryn Humphrey; Rod Humerickhouse; Eugen Tausch; Lukas Frenzel; Barbara Eichhorst; Clemens-M Wendtner; Stephan Stilgenbauer; Anton W Langerak; Jacque J M van Dongen; Sebastian Böttcher; Matthias Ritgen; Valentin Goede; Mehrdad Mobasher; Michael Hallek Journal: Blood Date: 2017-03-21 Impact factor: 22.113
Authors: John C Byrd; Joseph M Flynn; Thomas J Kipps; Michael Boxer; Kathryn S Kolibaba; David J Carlile; Guenter Fingerle-Rowson; Nicola Tyson; Jamie Hirata; Jeff P Sharman Journal: Blood Date: 2015-10-15 Impact factor: 22.113
Authors: Susan M O'Brien; Nicole Lamanna; Thomas J Kipps; Ian Flinn; Andrew D Zelenetz; Jan A Burger; Michael Keating; Siddhartha Mitra; Leanne Holes; Albert S Yu; David M Johnson; Langdon L Miller; Yeonhee Kim; Roger D Dansey; Ronald L Dubowy; Steven E Coutre Journal: Blood Date: 2015-10-15 Impact factor: 22.113
Authors: Stephan Stilgenbauer; Barbara Eichhorst; Johannes Schetelig; Steven Coutre; John F Seymour; Talha Munir; Soham D Puvvada; Clemens-Martin Wendtner; Andrew W Roberts; Wojciech Jurczak; Stephen P Mulligan; Sebastian Böttcher; Mehrdad Mobasher; Ming Zhu; Monali Desai; Brenda Chyla; Maria Verdugo; Sari Heitner Enschede; Elisa Cerri; Rod Humerickhouse; Gary Gordon; Michael Hallek; William G Wierda Journal: Lancet Oncol Date: 2016-05-10 Impact factor: 41.316
Authors: Andrew W Roberts; Matthew S Davids; John M Pagel; Brad S Kahl; Soham D Puvvada; John F Gerecitano; Thomas J Kipps; Mary Ann Anderson; Jennifer R Brown; Lori Gressick; Shekman Wong; Martin Dunbar; Ming Zhu; Monali B Desai; Elisa Cerri; Sari Heitner Enschede; Rod A Humerickhouse; William G Wierda; John F Seymour Journal: N Engl J Med Date: 2015-12-06 Impact factor: 91.245
Authors: Ian W Flinn; Amy S Ruppert; William Harwin; David Waterhouse; Steven Papish; Jeffrey A Jones; John Hainsworth; John C Byrd Journal: Am J Hematol Date: 2016-07-22 Impact factor: 10.047
Authors: Daniel R Richardson; Norah L Crossnohere; Jaein Seo; Elihu Estey; Bernadette O'Donoghue; B Douglas Smith; John F P Bridges Journal: Cancer Epidemiol Biomarkers Prev Date: 2020-03-04 Impact factor: 4.254