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Sequential treatment with bendamustine, obinutuzumab (GA101) and Ibrutinib in chronic lymphocytic leukemia (CLL): final results of the CLL2-BIG trial

To the Editor:

The prospective, open-label, multicenter phase II trial CLL2-BIG (registered at as # NCT02345863) was the first of the so called BXX trials of the German CLL Study Group (GCLLSG) [1] designed according to the “sequential triple-T” concept of a tailored and targeted treatment aiming at total eradication of minimal residual disease (MRD) [2]. These trials aimed to evaluate novel combination therapies using CD20-antibodies such as obinutuzumab (GA101) and targeted drugs such as ibrutinib with a limited duration of treatment in an all comer population irrespective of firstline (1 L) versus relapse/refractory (RR) therapy, comorbidities and genetic features. Patients with a higher tumor load received two courses of bendamustine as debulking before six cycles of induction therapy (IT) with obinutuzumab and ibrutinib were administered. Patients responding to IT continued with maintenance therapy (MT), consisting of daily ibrutinib and obinutuzumab every three months until achievement of an undetectable MRD (uMRD) remission by flow cytometry (10^−4), confirmed by two consecutive uMRD results in the peripheral blood (PB) within three months, progression, start of new therapy or for up to 24 months, whichever occurred first.

The primary endpoint analysis with an overall response rate of 100% including 47.5% patients with uMRD in PB at the end of IT has been reported previously [3]. Here, we present the final analysis with extended follow-up including the maintenance phase and data on treatment discontinuation triggered by MRD assessment in PB.

61 patients (30 1 L (49.2%), 31 RR (50.8%)) constituted the full analysis set that was defined as all enrolled patients who received at least two complete cycles of IT and used for efficacy analyses according to the study protocol. Safety analyses included all 66 recruited patients who received at least one dose of any compound of the study treatment. Patient demographics are shown in Table 1. After a median observation time of 38.1 months (range 5.4–44.8; 1 L 38.5, RR 37.2) 49 patients (80.3%; 28 1 L, 21 RR) completed the trial as planned. As one RR patient died during IT and another RR patient underwent adverse events (AE) that prohibited further study treatment, 59 of 61 patients (96.7%; 30 1 L, 29 RR) started MT. A median of three maintenance cycles were administered (range 1–8).

Table 1 Patient Demographic and Baseline Clinical Characteristics.

15 patients (25.4%; 6 1 L, 9 RR) completed 24 months of MT. 11 patients discontinued early: 6 due to AE (10.2%; 2 1 L, 4 RR), 2 each (3.4%) due to PD (2 RR) or refusal of further treatment (2 1 L) and 1 RR due to physician´s decision (1.7%).

33 patients (55.9%; 20 1 L, 13 RR) terminated MT due to uMRD in PB after a median time on MT of 6.0 months (range 3.0–23.3; 1 L: 6.2 months, RR: 5.7 months).

During MT, response was improved in 16 of 59 patients (27.1%) with 6 patients (10.2%) achieving a complete remission (CR) or CR with incomplete recovery of the bone marrow (BM) as best response [4]. 53 patients (89.8%) achieved a partial remission including 32 patients (54.2%) with a clinical CR defined as absence of disease by clinical examination and blood count, but without computed tomography assessment or BM biopsy. 42 of 59 patients (23 1 L, 19 RR) had uMRD in PB at the last staging during MT resulting in an uMRD rate of 71.2% (1 L 76.7%, RR 65.5%). 56.3% of patients without and 76.7% of patients with prior debulking therapy reached uMRD at the last staging during MT.

The median duration of response (DOR) was 38.0 months and the 2-year DOR rate 88.3% (1 L 100.0%, RR 77.4%). The median time to uMRD from the date of enrolment to the date of first uMRD was 10.9 months (1 L 10.2 months, RR 10.9 months) as the first measurement took place after 8 months. The median event free survival (EFS) was 44.8 months with a 3-year EFS rate of 70.9% (1 L 81.8%, RR 60.7%), the median treatment free survival and median time to next treatment were not reached with a 3-year rate of 76.1% (1 L 89.0%, RR 64.0%) and 83.2% (1 L 89.0%, 77.2%), respectively. However, 9 patients (14.8%) received further treatment after the end of the trial (3 1 L (10.0%), 6 RR (19.4%)). Subsequent therapies consisted of chemoimmunotherapy or venetoclax plus obinutuzumab. Five patients (2 1 L, 3 RR) received subsequent therapies with ibrutinib.

The estimated median progression free survival (PFS) was 44.8 months with 77.9% (1 L 89.1%, RR 67.3%) being event-free at 3 years (HR 0.230, 95% CI 0.064–0.828; Fig. 1a). Seven of 17 patients without (41.2%) and 8 of 44 patients with prior debulking (18.2%) progressed or died. At 3-years, 57.8% of patients without and 85.7% of patients with debulking were still event-free (HR 0.251, CI 0.084–0.751), In 13 patients with TP53 aberrations (i.e. TP53 mutation and/or 17p deletion) 3 (23.1%, 0 1 L, 3 RR) and in 48 patients without genetic TP53 aberrations 12 events occurred (25%). The PFS rate at 2 years was 76.9% for patients with TP53 aberrations versus 95.8% for patients without (HR 1.076, 95% CI 0.3–3.86).

Fig. 1: Time to event endpoints.
figure 1

a shows the estimated progression free survival (PFS) for patients of the full analysis set (FAS); first line patients are marked in blue, relapsed/refractory patients in green. b shows the estimated overall survival (OS) for patients of the full analysis set (FAS); first line patients are marked in blue, relapsed/refractory patients in green.

In a landmark analysis from last treatment exposure during MT, the median PFS was not reached in patients who stopped MT due to uMRD with a 2-year PFS rate of 82.9%. Five patients with TP53 aberrations discontinued MT due to uMRD with one progression occuring after 6.2 months after treatment discontinuation. 8 patients with TP53 aberrations discontinued MT for other reasons than uMRD with two progressions (25.0%).

In another extended PFS landmark analysis of patients with unmutated IGHV status who discontinued MT for other reasons, only one progression occurred in 10 patients (10.0%) with prior debulking versus 3 progressions in 8 patients (37.5%) without debulking (HR 0.039, CI 0.003–0.553).

Seven patients died (11.5%) with no deaths occurring in 1 L patients. Causes of deaths included two events of sepsis and one event of pulmonary sepsis, duodenitis, pneumonia and cerebrovascular accident each. One patient died due to PD. No grade 5 AE occurred during MT. Two patients with TP53 aberrations and very high CLL-IPI died after discontinuation of MT for other reasons than uMRD; one due to AE, one due to PD. One fatality occurred after treatment discontinuation due to uMRD. Overall survival is shown in Fig. 1b.

During MT, 332 CTC grades 1–4 AE were documented. Adjustment of study drugs was performed due to 79 (23.8%) events whereas AE related dose modifications of ibrutinib occurred in 26 patients (44.1%; 15 1 L (50.0%), 11 RR (37.9%)). Most events (85 (25.6%)) were infections or infestations followed by skin and subcutaneous tissue disorders (32 (9.6%)) and gastrointestinal disorders (30 (9.0%)). Most common observed grade 3–4 toxicities during MT were neutropenia (in 11.9% of patients; 1 L 13.3%, RR 10.3%), basal cell carcinoma (in 6.8% of patients; 1 L 13.3%, RR 0), thrombocytopenia (in 5.1% of patients; 1 L 3.3%, RR 6.9%) and pneumonia (in 5.1% of patients; 1 L 6.7%, RR 3.4%). All infections were CTC grade 3 at maximum including one case of fungal pneumonia (CTC grade 3).

17 cases of cardiac disorders were documented, among them 6 cases of atrial fibrillation. 13 bleeding events occurred in 11 of 59 (18.6%) patients.

In conclusion, the CLL2-BIG study demonstrated that sequential therapy with bendamustine, ibrutinib and obinutuzumab showed a very promising efficacy and good safety profile. With the addition of obinutuzmab, no additional toxicity occurred when compared to ibrutinib monotherapy [5] and no increase of bleeding or cardiac events was observed.

By continuation of ibrutinib and obinutuzumab during MT the depth of response could be improved as previously shown for treatment with ibrutinib [5, 6]. Notably, 71.2% of the patients had uMRD in PB at the last staging during MT which is comparable with uMRD rates after venetoclax containing combination regimens [7, 8].

However, even with a longer follow-up this trial will not answer the question whether a fixed-duration treatment is superior to a long-term therapy due to the lack of a randomized, direct comparison. This will be addressed in future trials, e.g. the CLL17 trial (registered at as #NCT04608318).

Nevertheless, even though treatment could be discontinued early, a 3-year PFS rate of 77.9% for the BIG regimen seems comparable with first line treatment with obinutuzumab and ibrutinib as long-term therapy in the ILLUMINATE trial with an estimated 30-month PFS of 79% [9].

Though, our results show that an MRD-guided treatment discontinuation of ibrutinib is promising and feasible for different CLL patient groups including those with unfavorable risk factors. However, it remains to be determined which patients of this heterogeneous study population may have benefited the most.

Prior debulking therapy might be beneficial, possibly due to rapid achievement of uMRD, broad selective pressure or prevention of clonal sweeps caused by prior application of chemotherapy. Whether this is really playing a significant role in overcoming adverse outcomes, especially in patients with unmutated IGHV status or TP53 aberrations, needs further evaluation.

Therefore, pooled analyses across the BXX trials will be performed. Additionally, a second generation of BXX trials is currently conducted.

Ultimately, these conceptual trials will allow to design more personalized approaches for future CLL therapies.


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This study was initiated and organized by the German CLL Study Group as an academic trial with the University of Cologne being the sponsor, and financial support by F. Hoffmann-La Roche Ltd and Janssen-Cilag. The authors wish to express their gratitude towards all patients participating in the trial and their families, as well as the physicians and trial staff at the sites. Furthermore, we thank all study team members involved; in particular, we acknowledge Johanna Wesselmann and Irene Stodden for their excellent contribution. Finally, we thank Dr. Birgit Fath and the monitors from the competence network malignant lymphoma (“Kompetenznetz Maligne Lymphome”) for facilitating the conduct of this trial.


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Authors and Affiliations



JvT, PC, BE, and MH designed the research, treated patients, collected, analyzed and interpreted the data and wrote the paper. SR analyzed and interpreted the data, performed the statistical analysis and wrote the paper. KF designed the research, analyzed and interpreted the data and wrote the paper. PL, A-MF, OA-S and MF analyzed and interpreted the data and wrote the paper. K-AK, AT, SS, SB and MR treated patients, were responsible for the central laboratory tests, analyzed and interpreted the data. treated patients, were responsible for the central laboratory tests, analyzed and interpreted the data. C-MW treated patients and interpreted the data. TI and HK treated patients. All authors critically reviewed the paper and approved the final version.

Corresponding author

Correspondence to Julia von Tresckow.

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Competing interests

JvT: honoraria (AbbVie, AstraZeneca, Janssen, Roche); research funding (Janssen, Roche); PC: consulting fees (AbbVie, Acerta, AstraZeneca), honoraria (AbbVie, AstraZeneca, Janssen, Roche), travel support (AbbVie, AstraZeneca, Gilead, Janssen, Roche), research support (AbbVie, AstraZeneca, BeiGene, Gilead, Janssen, Novartis/GSK, Roche); SR: nothing to disclose; PL: research funding (Janssen-Cilag), Consulting fees (Janssen-Cilag, AbbVie, Astra Zeneca), honoraria (Janssen-Cilag, AbbVie, Astra Zeneca), travel support (Janssen-Cilag, AbbVie, Astra Zeneca); AMF: Celgene (Research grant), AbbVie (Travel Support), Janssen (Advisory Board); OAS: Janssen (Personal fees, honoraria, research funding), Roche (Personal fees, honoraria, research funding), AbbVie (Personal fees, honoraria, research funding), BeiGene (Honoraria, research funding), AstraZeneca (Personal fees, honoraria), Gilead (Personal fees, honoraria); MF: nothing to disclose; TI: nothing to disclose; HK: nothing to disclose; ET: Consulting fees (Roche, Abbvie, Janssen), honoraria (Roche, Abbvie, Janssen), payment for expert testimony (Roche, Abbvie, Janssen), travel support (Janssen, AbbVie); MR: personal fees from Hoffman-La Roche (advisory board) and nonfinancial support from Celgene; KF: Honoraria (AbbVie, Roche), travel grants (Roche); CMW: Grants (Hoffmann-La Roche, Cilag-Janssen, AbbVie, Gilead, AstraZeneca), consulting fees (Hoffmann-La Roche, Cilag-Janssen, AbbVie, Gilead, AstraZeneca), honoraria (Hoffmann-La Roche, Cilag-Janssen, AbbVie, Gilead, AstraZeneca), travel support (Hoffmann-La Roche, Cilag-Janssen, AbbVie, Gilead, AstraZeneca), Participation on a Data Safety Monitoring Board or Advisory Board (Hoffmann-La Roche, Cilag-Janssen, AbbVie, Gilead, AstraZeneca); KAK: Mundipharma, Roche, Janssen (Speaker’s bureau, Honoraria, Resarch support, Consulting); SS: Advisory board honoraria (AbbVie, Amgen, AstraZeneca, Celgene, Gilead, GSK, Hoffmann-La Roche, Janssen, Novartis, Sunesis), Research support (AbbVie, Amgen, AstraZeneca, Celgene, Gilead, GSK, Hoffmann-La Roche, Janssen, Novartis, Sunesis), Travel support (AbbVie, Amgen, AstraZeneca, Celgene, Gilead, GSK, Hoffmann-La Roche, Janssen, Novartis, Sunesis), Speaker fees (AbbVie, Amgen, AstraZeneca, Celgene, Gilead, GSK, Hoffmann-La Roche, Janssen, Novartis, Sunesis); SB: Janssen (research support), honoraria (Roche, AbbVie, Norvatis, Becton Dickonson, Janssen, Astra Zeneca, Sanofi); BE: grants and personal fees (Janssen-Cilag, Roche, Abbvie and Gilead), personal fees (Novartis, Celgene, ArQule, AstraZeneca and Oxford Biomedica (UK)), grants (BeiGene); MH: personal fees and other (AbbVie, Celgene, Gilead Sciences, Janssen, Mundipharma, Pharmacyclics, Roche).

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von Tresckow, J., Cramer, P., Robrecht, S. et al. Sequential treatment with bendamustine, obinutuzumab (GA101) and Ibrutinib in chronic lymphocytic leukemia (CLL): final results of the CLL2-BIG trial. Leukemia 36, 2125–2128 (2022).

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