TY - JOUR
T1 - Ibrutinib plus rituximab and mini-CHOP in older patients with newly diagnosed DLBCL
T2 - a phase 2 ALLG study
AU - Australasian Leukaemia & Lymphoma Group
AU - Verner, Emma
AU - Johnston, Amanda
AU - Pati, Nalini
AU - Hawkes, Eliza A.
AU - Lee, Hui Peng
AU - Cochrane, Tara
AU - Cheah, Chan Yoon
AU - Filshie, Robin
AU - Purtill, Duncan
AU - Sia, Hanlon
AU - Enjeti, Anoop K.
AU - Brown, Christina
AU - Murphy, Nicholas
AU - Curnow, Jennifer
AU - Lee, Kenneth
AU - Gandhi, Maher K.
AU - Walia, Mannu
AU - Butcher, Belinda E.
AU - Trotman, Judith
N1 - Publisher Copyright:
© 2024 by The American Society of Hematology.
PY - 2024/11/12
Y1 - 2024/11/12
N2 - The multicenter, prospective phase 2 Australasian Leukaemia & Lymphoma Group NHL29 trial was conducted to assess the addition of ibrutinib to R-mini-CHOP (dose attenuated R-CHOP; rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in patients aged ≥75 years with newly diagnosed diffuse large B-cell lymphoma (DLBCL). Treatment consisted of six 21-day cycles of ibrutinib–R-mini-CHOP followed by two 21-day cycles of R-ibrutinib. Coprimary end points were deliverability and 2-year overall survival (OS). The median average relative total dose and average relative dose intensity for the entire regimen were both 97% (interquartile range, 82-100 and 88-100, respectively). With a median follow-up of 35.5 months, the 2-year OS was 68% (95% confidence interval [CI], 55.6-77.4) with a 2-year progression-free survival (PFS) of 60.0% (95% CI, 47.7-70.3). Median OS and PFS were 72 months (95% CI, 35 to not reached) and 40 months (95% CI, 20.4 to not reached), respectively. The overall response rate was 76% (61/79) of patients, with a complete response rate of 71% (56/79). Deaths occurred in 34 of 79 patients (43%), including 17 from progressive disease and 5 treatment related. Overall, 67% patients experienced at least 1 serious adverse event. Most common adverse events were infections and diarrhea (the majority grade 1-2). In both health-related quality of life measures, there was an improvement in functional and symptom scales, median health state classification score, and median visual analogue scale in responders over time. In conclusion, this study showed that the addition of ibrutinib to R-mini-CHOP was both deliverable and efficacious in elderly DLBCL patients.
AB - The multicenter, prospective phase 2 Australasian Leukaemia & Lymphoma Group NHL29 trial was conducted to assess the addition of ibrutinib to R-mini-CHOP (dose attenuated R-CHOP; rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in patients aged ≥75 years with newly diagnosed diffuse large B-cell lymphoma (DLBCL). Treatment consisted of six 21-day cycles of ibrutinib–R-mini-CHOP followed by two 21-day cycles of R-ibrutinib. Coprimary end points were deliverability and 2-year overall survival (OS). The median average relative total dose and average relative dose intensity for the entire regimen were both 97% (interquartile range, 82-100 and 88-100, respectively). With a median follow-up of 35.5 months, the 2-year OS was 68% (95% confidence interval [CI], 55.6-77.4) with a 2-year progression-free survival (PFS) of 60.0% (95% CI, 47.7-70.3). Median OS and PFS were 72 months (95% CI, 35 to not reached) and 40 months (95% CI, 20.4 to not reached), respectively. The overall response rate was 76% (61/79) of patients, with a complete response rate of 71% (56/79). Deaths occurred in 34 of 79 patients (43%), including 17 from progressive disease and 5 treatment related. Overall, 67% patients experienced at least 1 serious adverse event. Most common adverse events were infections and diarrhea (the majority grade 1-2). In both health-related quality of life measures, there was an improvement in functional and symptom scales, median health state classification score, and median visual analogue scale in responders over time. In conclusion, this study showed that the addition of ibrutinib to R-mini-CHOP was both deliverable and efficacious in elderly DLBCL patients.
UR - http://www.scopus.com/inward/record.url?scp=85209922790&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2024014035
DO - 10.1182/bloodadvances.2024014035
M3 - Article
C2 - 39226464
AN - SCOPUS:85209922790
SN - 2473-9529
VL - 8
SP - 5674
EP - 5682
JO - Blood advances
JF - Blood advances
IS - 21
ER -