Scientific Letters
Keywords: Chronic lymphocytic leukaemia; Pseudo-richter; BTK inhibitors; Zanubrutinib.
| Published: September 01, 2026 | Received: July 22, 2026 | Accepted: August 04, 2026 |
Citation: Laurenti L., Quaranta T., Tomasso A., Stirparo L., Abbate P.L., Bakacs A., Cappoli N., Di Napoli A., Efremov D., Bellisario F., Gattei V., Caldarella C., Calcagni M.L., Autore F., Innocenti I. A case of Pseudo-Richter Transformation following zanubrutinib discontinuation in CLL. Mediterr J Hematol Infect Dis 2026, 18(1): e2026070, DOI: http://dx.doi.org/10.4084/MJHID.2026.070
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Covalent Bruton tyrosine kinase inhibitors (cBTKi), including ibrutinib, acalabrutinib, and zanubrutinib, are highly effective in both treatment-naïve and relapsed/refractory Chronic Lymphocytic Leukemia (CLL), producing durable disease control and significant improvements in progression-free and overall survival compared with conventional chemoimmunotherapy regimens Consequently, they have become a cornerstone of CLL management and are generally administered continuously until disease progression or unacceptable toxicity. The efficacy of cBTKi relies on sustained target inhibition, making long-term continuous therapy an essential of treatment However, temporary treatment interruptions are common in clinical practice, occurring in up to 40% of patients (pts) the most frequent indication being the need for invasive or surgical procedures. Hemorrhage emerged as a notable adverse event during early clinical trials of ibrutinib, leading to recommendations that the drug be withheld for 3–7 days before and after surgery, depending on the anticipated bleeding risk Additional causes of treatment interruption include infections, hematologic and nonhematologic toxicities, and clinically significant drug–drug interactions requiring temporary discontinuation or dose modification. Emerging evidence suggests that temporary cessation of cBTKi therapy may trigger rapid disease reactivation, often referred to as “disease flare,” characterized by worsening constitutional symptoms, enlarging lymphadenopathy, and laboratory evidence of increased disease activity A particularly challenging manifestation of this phenomenon is pseudo-Richter transformation (pseudo-RT), an uncommon but clinically important syndrome characterized by a transient proliferation of large, atypical B cells that closely mimics Richter transformation (RT) both clinically and histopathologically Most reported cases occur in patients with previously stable CLL/SLL, who develop symptoms within 1–2 weeks of cBTKi interruption; however, presentations as early as 48 hours after treatment cessation have been described. Clinical manifestations commonly include rapidly enlarging lymphadenopathy, constitutional (“B”) symptoms, lymphocytosis, and elevated serum lactate dehydrogenase (LDH) levels some patients do not show any constitutional symptoms, others exhibit painful lymphadenopathy, akin to inflammatory/infectious diseases. Unlike true RT, however, pseudo-RT follows a reversible course and typically resolves after reinitiation of cBTKi therapy, without the need for chemotherapy. Despite increasing recognition of pseudo-RT, its incidence, pathobiology, and clinical characteristics remain poorly defined.
We introduce a 75-year-old man with CLL carrying unmutated IGHV 1-69 and a NOTCH1 mutation, without TP53 aberrations or del(17p), who was initially treated in first line with the ibrutinib-venetoclax combination, achieving a complete remission. Approximately 15 months after completing treatment, he experienced disease progression characterized by recurrent lymphocytosis, lymphadenopathy, and splenomegaly. Molecular reassessment confirmed absence of TP53 abnormalities and did not detect resistance mutations involving BTK or PLCG2. He was started on zanubrutinib in December 2024. The patient achieved a deep clinical and hematologic response, with normalization of blood counts and marked reduction of disease burden. In April 2026, zanubrutinib was temporarily discontinued because of grade 3 hepatotoxicity, with alanine aminotransferase (ALT) over 5 times above the upper normal value and mild hyperbilirubinemia. At the same time, a mesenteric lesion adjacent to a jejunal loop was identified on surveillance imaging and was considered suspicious for a gastrointestinal stromal tumor (GIST). A ^18F-FDG PET/CT scan was performed 9 days after zanubrutinib suspension, as part of the diagnostic work-
Figure 1. Panel A-B: comparison between FDG PET/CT on April 2026, at zanubrutinib discontinuation (A) and four weeks after restarting therapy (B). Panel C-D: excisional inguinal lymph node biopsy, stained with hematoxylin and eosin, original magnification 2.9X (C) and 28.2X (D). Panel E: Immunohistochemical staining for Ki-67, 11.8X. Panel F: Immunohistochemical staining for CD5, 9.4X. Panel G: Immunohistochemical staining for CD23, 12.1X.
up of the suspected GIST; it demonstrated widespread, intensely hypermetabolic lymphadenopathy involving cervical, supraclavicular, axillary, mediastinal, abdominal, pelvic, and inguinal nodal stations (Figure 1, panel A). The highest metabolic activity was observed in the right internal iliac lymph node (SUVmax 48.1), left obturator lymph node (SUVmax 46.6), bilateral cervical level IIa lymph nodes (SUVmax 41.2 and 40.2), and the interportocaval region (SUVmax 41.1). Additional highly avid mediastinal nodes showed SUVmax values up to 40.0 The scan also revealed diffuse splenic involvement with splenomegaly (18 cm, SUVmax 21.6). Blood cell count showed a WBC count of 25 x 10^3/mm3, with 41% atypical, medium/large-sized lymphocytes with occasional nucleoli. No cytopenia was reported. Serum LDH was moderately elevated (twice the upper normal value). Serum calcium levels were within the normal range. The patient had experienced no systemic symptoms or signs of clinical deterioration. An excisional inguinal lymph node biopsy was performed, which showed diffuse proliferation of large B cells with a high proliferative index (Ki-67 approximately 80%), consistent with RT (Figure 1, panels C-E). The following immunophenotype was demonstrated: CD3-, CD20+, CD79a+, CD5+, CD23+/-, bcl2+, MUM1+/-, CD10-, bcl6+/-, CyclinD1-, CD30+/-, CD38-, PD1+/-, ALK-, p53+ (5%), c-myc+ (15%) (Figure 1, panels F-G). Molecular analysis of the lymph node biopsy using Multiplex Ligation-dependent Probe Amplification (MLPA) to assess common CLL mutations and copy number alterations did not identify any additional genetic lesions beyond the NOTCH1 mutation. NGS sequencing of the variable region of the IGHV through PCR confirmed that the large-cell proliferation was clonally related to the underlying CLL clone. Because of the clinical suspicion of pseudo-RT, 18 days after discontinuation, zanubrutinib was reintroduced at a reduced dose of 80 mg twice daily, due to a grade 2 transaminase elevation still being present. It resulted in a striking clinical and metabolic response: a PET/CT performed four weeks later demonstrated near-complete resolution of the previously extensive hypermetabolic lymphadenopathy above and below the diaphragm, disappearance of extranodal lesions, and marked reduction of splenomegaly, consistent with a complete metabolic response (Deauville score 2) (Figure 1, panel B). In June, the patient underwent mid-distal jejunal resection to remove the suspected GIST. Histopathology confirmed a spindle-cell jejunal GIST (CD117+, DOG1+, S100-), with a mitotic rate of 2 per 5 mm2 and small B-cell lymphocytic aggregates (CD20+, CD5+, CD23+). Both proximal and distal resection margins were clear of disease. At the time of writing, at 2-month follow-up, the patient is in full nodal/organ response, with complete resolution of hypertransminasemia and an absolute lymphocyte count of 8,000/µL.
Disease flares after cBTKi discontinuation have been described in patients with CLL as well as in other B-cell malignancies, including Waldenström macroglobulinemia, and have been reported to resolve upon resumption of cBTKi therapy.6,11 These observations underscore the dependence of disease control on continuous BTK pathway inhibition. The term “pseudo-RT” was coined in 2020, when Barnea Slonim et al. first reported 5 cases of biopsy-proven RT developing immediately after ibrutinib discontinuation; notably, 4/5 pts had trisomy 12, and the remaining one had del17p; the patients retained a CLL-like immunophenotype, with preserved CD5 and CD23 expression; they achieved response after restarting ibrutinib. Hampel et al. reported 3 cases of pseudo-RT after ibrutinib interruption, in patients undergoing lymph node examination for second malignancies; they all expressed unmutated IGHV and were positive for TP53 mutation; they were successfully restarted on ibrutinib. In 2024, the Mayo Clinic group first reported a case ofpseudo-RT after acalabrutinib discontinuation A recent systematic review of 2026 by the University of Murcia reported 15 pts with pseudo-RT after ibrutinib or acalabrutinib discontinuation: most patients showed a high proliferation index (Ki-67 50-90%), non-germinal center phenotype, retained CD5/CD23 expression, high risk characteristics (unmutated IGHV in 100% cases, TP53 mutation in 4/6 and NOTCH1 in 1/6 analyzed pts). To our knowledge, this is the first reported case of pseudo-RT following zanubrutinib discontinuation. Notably, several molecular features described in patients with pseudo-RT, such as NOTCH1 alterations and TP53 abnormalities, have also been associated with an increased risk of RT Although the limited number of reported cases precludes definitive conclusions, these observations raise the possibility that pseudo-RT may preferentially occur in biologically high-risk CLL subsets. Our case further expands the biological spectrum of pseudo-RT by documenting its occurrence in a pt with NOTCH1-mutated, TP53-wild-type CLL. At the time of biopsy, the histopathological features fulfilled diagnostic criteria for true RT. However, several clinical nuances, such as the strict temporal association with zanubrutinib withdrawal and the relative lack of systemic symptoms, raised clinical suspicion of a disease flare. A rapid, complete metabolic response was observed, despite the aggressive morphological features and the identical clonal origin, a feature historically associated with treatment resistance and dismal outcomes in the setting of true RT It must be acknowledged that the distinction between true RT and pseudo-RT in this setting relies retrospectively on clinical reversibility as the principal diagnostic criterion. The striking response observed merely four weeks after zanubrutinib reintroduction strongly supported the diagnosis of pseudo-RT ex juvantibus.
The rapid onset of clinically, radiologically, and histologically aggressive disease following zanubrutinib discontinuation, together with its prompt and complete metabolic remission after cBTKi reintroduction, supports the existence of a reversible pseudo-RT phenomenon that can closely mimic true RT. Clinicians should consider it as a key differential diagnosis whenever a patient presents with a Richter-like flare shortly after the interruption or discontinuation of a BTKi. Awareness of this entity is crucial to avoid escalation to intensive chemotherapy and to consider prompt cBTKi resumption whenever clinically feasible. Further studies are needed to identify objective markers to distinguish pseudo-RT from true RT. Additional long-term follow-up of reported cases is warranted to determine whether pseudo-RT might represent an early stage in the evolution toward overt RT and, finally, whether pts experiencing this syndrome are at increased risk of subsequent CLL/SLL progression.
The datasets analyzed during the current study are not publicly available due to patient confidentiality considerations but are available from the corresponding author on reasonable request and subject to applicable ethical and institutional requirements.
The authors declare no competing interest.
Correspondence to: Tommaso Quaranta. Università Cattolica del Sacro Cuore, Istituto di Ematologia, Roma, Italy. E-mail: tommasoquarantamd@gmail.com