Venetoclax and obinutuzumab in patients with CLL and coexisting conditions
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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Venetoclax and obinutuzumab in patients with CLL and coexisting conditions. / Fischer, K.; Al-Sawaf, O.; Bahlo, J.; Fink, A. M.; Tandon, M.; Dixon, M.; Robrecht, S.; Warburton, S.; Humphrey, K.; Samoylova, O.; Liberati, A. M.; Pinilla-Ibarz, J.; Opat, S.; Sivcheva, L.; Le Dû, K.; Fogliatto, L. M.; Niemann, C. U.; Weinkove, R.; Robinson, S.; Kipps, T. J.; Boettcher, S.; Tausch, E.; Humerickhouse, R.; Eichhorst, B.; Wendtner, C. M.; Langerak, A. W.; Kreuzer, K. A.; Ritgen, M.; Goede, V.; Stilgenbauer, S.; Mobasher, M.; Hallek, M.
I: New England Journal of Medicine, Bind 380, Nr. 23, 2019, s. 2225-2236.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Venetoclax and obinutuzumab in patients with CLL and coexisting conditions
AU - Fischer, K.
AU - Al-Sawaf, O.
AU - Bahlo, J.
AU - Fink, A. M.
AU - Tandon, M.
AU - Dixon, M.
AU - Robrecht, S.
AU - Warburton, S.
AU - Humphrey, K.
AU - Samoylova, O.
AU - Liberati, A. M.
AU - Pinilla-Ibarz, J.
AU - Opat, S.
AU - Sivcheva, L.
AU - Le Dû, K.
AU - Fogliatto, L. M.
AU - Niemann, C. U.
AU - Weinkove, R.
AU - Robinson, S.
AU - Kipps, T. J.
AU - Boettcher, S.
AU - Tausch, E.
AU - Humerickhouse, R.
AU - Eichhorst, B.
AU - Wendtner, C. M.
AU - Langerak, A. W.
AU - Kreuzer, K. A.
AU - Ritgen, M.
AU - Goede, V.
AU - Stilgenbauer, S.
AU - Mobasher, M.
AU - Hallek, M.
PY - 2019
Y1 - 2019
N2 - Background: The BCL2 inhibitor venetoclax has shown activity in patients with chronic lymphocytic leukemia (CLL), but its efficacy in combination with other agents in patients with CLL and coexisting conditions is not known. Methods: In this open-label, phase 3 trial, we investigated fixed-duration treatment with venetoclax and obinutuzumab in patients with previously untreated CLL and coexisting conditions. Patients with a score of greater than 6 on the Cumulative Illness Rating Scale (scores range from 0 to 56, with higher scores indicating more impaired function of organ systems) or a calculated creatinine clearance of less than 70 ml per minute were randomly assigned to receive venetoclax-obinutuzumab or chlorambucil- obinutuzumab. The primary end point was investigator-assessed progression- free survival. The safety of each regimen was also evaluated. Results: In total, 432 patients (median age, 72 years; median Cumulative Illness Rating Scale score, 8; median creatinine clearance, 66.4 ml per minute) underwent randomization, with 216 assigned to each group. After a median follow-up of 28.1 months, 30 primary end-point events (disease progression or death) had occurred in the venetoclax-obinutuzumab group and 77 had occurred in the chlorambucil-obinutuzumab group (hazard ratio, 0.35; 95% confidence interval [CI], 0.23 to 0.53; P<0.001). The Kaplan-Meier estimate of the percentage of patients with progression- free survival at 24 months was significantly higher in the venetoclax-obinutuzumab group than in the chlorambucil-obinutuzumab group: 88.2% (95% CI, 83.7 to 92.6) as compared with 64.1% (95% CI, 57.4 to 70.8). This benefit was also observed in patients with TP53 deletion, mutation, or both and in patients with unmutated immunoglobulin heavy-chain genes. Grade 3 or 4 neutropenia occurred in 52.8% of patients in the venetoclax-obinutuzumab group and in 48.1% of patients in the chlorambucil-obinutuzumab group, and grade 3 or 4 infections occurred in 17.5% and 15.0%, respectively. All-cause mortality was 9.3% in the venetoclax- obinutuzumab group and 7.9% in the chlorambucil-obinutuzumab group. These differences were not significant. Conclusions Among patients with untreated CLL and coexisting conditions, venetoclax-obinutuzumab was associated with longer progression-free survival than chlorambucil- obinutuzumab.
AB - Background: The BCL2 inhibitor venetoclax has shown activity in patients with chronic lymphocytic leukemia (CLL), but its efficacy in combination with other agents in patients with CLL and coexisting conditions is not known. Methods: In this open-label, phase 3 trial, we investigated fixed-duration treatment with venetoclax and obinutuzumab in patients with previously untreated CLL and coexisting conditions. Patients with a score of greater than 6 on the Cumulative Illness Rating Scale (scores range from 0 to 56, with higher scores indicating more impaired function of organ systems) or a calculated creatinine clearance of less than 70 ml per minute were randomly assigned to receive venetoclax-obinutuzumab or chlorambucil- obinutuzumab. The primary end point was investigator-assessed progression- free survival. The safety of each regimen was also evaluated. Results: In total, 432 patients (median age, 72 years; median Cumulative Illness Rating Scale score, 8; median creatinine clearance, 66.4 ml per minute) underwent randomization, with 216 assigned to each group. After a median follow-up of 28.1 months, 30 primary end-point events (disease progression or death) had occurred in the venetoclax-obinutuzumab group and 77 had occurred in the chlorambucil-obinutuzumab group (hazard ratio, 0.35; 95% confidence interval [CI], 0.23 to 0.53; P<0.001). The Kaplan-Meier estimate of the percentage of patients with progression- free survival at 24 months was significantly higher in the venetoclax-obinutuzumab group than in the chlorambucil-obinutuzumab group: 88.2% (95% CI, 83.7 to 92.6) as compared with 64.1% (95% CI, 57.4 to 70.8). This benefit was also observed in patients with TP53 deletion, mutation, or both and in patients with unmutated immunoglobulin heavy-chain genes. Grade 3 or 4 neutropenia occurred in 52.8% of patients in the venetoclax-obinutuzumab group and in 48.1% of patients in the chlorambucil-obinutuzumab group, and grade 3 or 4 infections occurred in 17.5% and 15.0%, respectively. All-cause mortality was 9.3% in the venetoclax- obinutuzumab group and 7.9% in the chlorambucil-obinutuzumab group. These differences were not significant. Conclusions Among patients with untreated CLL and coexisting conditions, venetoclax-obinutuzumab was associated with longer progression-free survival than chlorambucil- obinutuzumab.
U2 - 10.1056/NEJMoa1815281
DO - 10.1056/NEJMoa1815281
M3 - Journal article
C2 - 31166681
AN - SCOPUS:85066980544
VL - 380
SP - 2225
EP - 2236
JO - New England Journal of Medicine
JF - New England Journal of Medicine
SN - 0028-4793
IS - 23
ER -
ID: 240637934