To the Editor:
Distinctive molecular patterns in the clonotypic B-cell receptor (BCR) classify patients with chronic lymphocytic leukemia (CLL) into immunogenetic subsets with consistent clinicobiological profiles . Around 15–25% of all CLL patients are characterized by a clonotypic immunoglobulin (IG) light chain rearrangement using IGLV3-21*01/*04, featuring a stereotyped somatic hypermutation (G110R) at the IGLJ-IGLC border site (IGLV3-21R110) [2,3,4]. Patients with IGLV3-21R110 CLL present more frequently with advanced disease and have short time to first treatment (TTFT) and overall survival (OS) . However, the predictive impact of the IGLV3-21R110 genotype is less clearly understood. In a recent analysis of two randomized trials that evaluated the efficacy of targeted agents, we did not observe differences in the response, minimal residual disease depth or progression-free survival (PFS) of IGLV3-21R110 patients, compared to all other patients, suggesting that targeted agents mitigate the adverse risk associated with IGLV3-21R110 CLL . In addition, a pooled analysis of trials demonstrated that, irrespective of their IGHV mutational status, patients with subset #2 CLL, which invariably carry an IGLV3-21R110 IG light chain, have shorter time to next treatment (TTNT) after chemoimmunotherapy-based treatment . However, to determine whether all IGLV3-21R110 CLL patients should, irrespective of IG heavy chain stereotypy, preferentially receive targeted agents, characterization of the predictive impact of the IGLV3-21R110 genotype in the context of chemotherapy-based treatment is pivotal.
Here, we assess the real-world prognosis of patients with IGLV3-21R110 CLL after first-line chemotherapy-based treatment. Patient samples were obtained from the biobank of the Leiden University Medical Center (n = 140), the Academic Medical Center Amsterdam Biobank for B cell malignancies (n = 25) and the HOVON-68 databank (n = 55), all approved by the respective institutional ethical review boards . All patients provided informed consent. The clonotypic IG light chain sequence was determined previously [2, 4]. All patients provided informed consent and all TTNT was defined as the interval between the first day of index therapy and the first day of a subsequent line of anti-leukemic therapy or Richter’s transformation, while OS was defined as the interval between the first day of index therapy and death. Survival analysis was performed using Kaplan–Meier estimation in R. Statistical significance was evaluated using omnibus and pairwise log-rank testing.
IG light chain sequencing and follow-up up data were available for 219/220 CLL patients. One patient, having received ibrutinib as first-line treatment, was excluded from the analysis. Patients were diagnosed between 1983–2019 and were treated between 1986–2022. The median follow-up time was 122 months. Baseline characteristics of the 218 patients are listed in Table 1. The IGLV3-21R110 genotype was present in 35/218 (16%) patients. Baseline demographics and the IGHV mutational status were well-balanced between the groups. In agreement with previous publications, trisomy 12 and del(17p) were exclusively present in patients without IGLV3-21R1102–4.
At time of data review, 33/35 (94%) of IGLV3-21R110 patients and 151/183 (83%) patients with any other light chain had progressed to therapy. As previously reported , TTFT was markedly shorter in patients with IGLV3-21R110 CLL, compared to CLL with mutated IGHV (M-CLL) (median TTFT 31.9 months [95% CI: 21.0–48.0] versus 183.0 months [95% CI: 121.1-NR], P < 0.0001). Indeed, median TTFT of IGLV3-21R110 patients was more similar to patients with U-CLL (U-CLL: 14.3 months, 95% CI: 9.7–28.5, P = 0.06). First-line treatment regimens were comparable in both groups, with most patients having received chlorambucil monotherapy (Table 1).
Notably, when including only patients that received chemotherapy-based treatment, stratification by IGLV3-21R110 genotype did not reveal significant differences in TTNT and OS (Fig. 1A, B) (IGLV3-21R110 vs any other light chain, median TTNT: 54.1 months [95% CI: 35.7-NR] vs 31.6 months [95% CI: 22.0–47.8], P = 0.3, median OS: 128.4 months [95% CI: 95.1-NR] vs 83.6 months [74.2–120.0], P = 0.5). When stratifying patients without IGLV3-21R110 by IGHV mutational status, IGLV3-21R110 CLL patients had significantly longer TTNT, but not OS, compared to patients with unmutated IGHV (U-CLL) (median TTNT 54.1 months [95%CI 35.7 -NR] versus 27.8 [18.5–44.6] months, P = 0.028, median OS 128.4 months [95%CI 95.1-NR] versus 80.1 months [71.7–101.0], P = 0.11), but not compared to patients with M-CLL (median TTNT 54.1 months [95%CI 35.7 -NR] versus 77.5 months [95% CI: 35.7-NR], P = 0.2, median OS 128.4 months [95% CI: 95.1-NR] versus 296.2 months [95% CI: 59.3-NR], P = 0.3) (Fig. 1C, D). Within the IGLV3-21R110 patient group, there were no significant differences in TTNT between patients with unmutated (U-IGLV3-21R110, n = 13) and mutated IGHV (M-IGLV3-21R110, n = 16) (54.1 months [95%CI 34.9-NR] versus 46.6 months [95%CI 32.4-NR], P = 0.8) (Fig. 1E). Whereas there was no difference in median TTNT between M-IGLV3-21R110 and M-CLL with other light chains (46.6 months [95% CI: 32.4-NR] vs 77.5 [95% CI: 35.7-NR], P = 0.5), the difference between U-IGLV3-21R110 and U-CLL with any other light chain approached statistical significance (54.1 months [95% CI: 34.9-NR] versus 27.8 months [95% CI: 18.5–44.6], P = 0.076) (Fig. 1E). As there were very few events per arm, a similarly stratified approach for OS was not feasible. In a separate analysis, including only patients receiving chlorambucil monotherapy, similar patterns were apparent, with IGLV3-21R110 signifying a group of patients with intermediate TTNT and OS, compared to patients with U-CLL and M-CLL (Supplementary Fig. 1). However, none of these differences reached statistical significance.
Due to a constrained cohort size and treatment heterogeneity, statistical power was limited in this real-world analysis. Furthermore, the most frequently used treatment regimen in this group, chlorambucil monotherapy, is no longer the recommended standard-of-care for the treatment of CLL. In addition, clinical response and PFS could not be reliably estimated due to irregular reporting of international workshop on CLL (iwCLL) criteria. Finally, as this analysis was retrospective in nature, confounding by indication cannot be fully excluded. That said, the documented baseline characteristics indicated that the cohorts are comparable.
In summary, these data suggest that in a real-world setting, IGLV3-21R110 CLL patients may, irrespective of their IGHV mutational status, have longer TTNT after chemotherapy-based treatment, compared to patients with U-CLL. This implies that IGLV3-21R110 may represent a mainly prognostic, but not predictive marker, signifying CLL with a short indolent phase that nevertheless responds favorably to both novel agents and chemotherapy-based treatment. The importance of classical stratification by IGHV mutational status in patients with IGLV3-21R110 CLL seems limited. Based on these intriguing observations, the question whether chemo(immuno)therapeutic and targeted agents are equally efficacious in IGLV3-21R110 CLL warrants further exploration in a more controlled setting, preferably in a randomized trial.
Data will be made available upon reasonable request to the corresponding author.
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The authors would like to thank all patients, physicians and investigators who participated in the LUMC biobank, the AMC biobank for B cell malignancies and the HOVON-68 trial.
JMND has received research funding from Roche/Genentech. APK has received research grants from Abbvie, AstraZeneca, BMS, Janssen and Roche Genentech and has performed Adboard activities for Abbvie, BMS, Janssen, LAVA and Roche Genentech. AWL has received research funding via an unrestricted grant from Roche-Genentech and speaker-fees from Janssen. M-DL has received personal fees from AbbVie, Janssen, and Roche; and research funding from AbbVie, Janssen, AstraZeneca, and Roche/Genentech. The remaining authors declare no competing financial interests.
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Hengeveld, P.J., Veelken, H., van Bergen, C.A.M. et al. Prognosis of IGLV3-21R110 chronic lymphocytic leukemia after chemotherapy-based treatment in a real-world analysis. Leukemia 37, 1929–1932 (2023). https://doi.org/10.1038/s41375-023-01975-0