Abstract 820P
Background
Waldenström's Macroglobulinemia (WM) presents heterogeneous clinical presentation and prolonged course, during which a second primary malignancy (SPM) or transformation to high grade lymphoma may occur post treatment initiation.
Methods
Symptomatic patients with WM were prospectively enrolled. The incidence of an SPM and the disease transformation post treatment initiation were recorded.
Results
668 patients were enrolled [median follow up: 186 months, median age: 71 years, males: 54%, 314 (47%) have died]. Primary treatment was rituximab-based in 63%, contained alkylating agents in 76%, a nucleoside analogue in 2%, proteasome inhibitors in 5% and Bruton’s tyrosine kinase (BTK) inhibitors in 10%. 58 patients (8.7%) were diagnosed with an SPM [prostate (22%), lung (21%), colon (9%), stomach (7%), pancreas (5%), head and neck (7%), central nervous system (7%), non-melanotic skin tumors (5%), skin melanoma (5%), ovarian (2%), thyroid (2%), hematologic malignancies (10%)]. The median time from treatment initiation to the diagnosis of an SPM or to transformation was 54 months. The incidence rate (IR) of an SPM was 0.008 per person-years. The cumulative incidence (CI), accounting for death due to WM or other causes as a competing event, at 5 and 10 years was 3.6% and 6.6%. The risk of death from WM or other causes was 22% and 45%, respectively. The IR of an SPM was higher in men (p=0.067), but no difference was recorded concerning the age or the agent used. 23 (3.4%) transformations were identified. The IR for transformation was 0.004 per person-years. The CI for transformation, accounting for death of any cause as a competing event, was 2.2% and 3.6% at 5 and 10 years respectively. The presence of anemia (hemoglobin<11.5gr/dl) at the time of diagnosis was associated with increased risk of transformation (p=0.02). The use of rituximab as a primary treatment decreased transformation risk (p=0.04).
Conclusions
The incidence of a SPM in symptomatic patients with WM post treatment initiation was 8.7%. Transformation to high grade lymphoma was 3.4%. This data emphasizes the need for screening for the most common malignancies among patients with WM, due to the prolonged survival of the disease.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
224P - Lung cancer scRNA-seq analyses reveal potential mechanisms causing different efficacy of target therapy and immunotherapy between EGFR 19del and L858R lung adenocarcinoma
Presenter: Hao Wang
Session: Poster session 09
225P - Nivolumab for cancer of unknown primary (CUP): Clinical efficacy and biomarker analysis from NivoCUP2 expanded access program (WJOG14620M)
Presenter: Junko Tanizaki
Session: Poster session 09
226TiP - CLEAR-Me: Interception trial to detect and clear molecular residual disease in patients with high-risk melanoma
Presenter: Erick Saldanha
Session: Poster session 09
227TiP - A phase II, open label, randomized, non-comparative cohorts study of adjuvant atezolizumab or atezolizumab plus tiragolumab in solid tumors with resectable disease with intermediate-high risk of recurrence and high tumor mutational burden (TMB-H) or microsatellite instability (MSI-H)
Presenter: Guillermo Antonio De Velasco Oria
Session: Poster session 09
228TiP - FINPROVE: The Finnish national study to facilitate patient access to targeted anti-cancer drugs
Presenter: Mika Mustonen
Session: Poster session 09
229TiP - A phase II trial of a neural network-based treatment decision support tool in patients (pts) with refractory solid organ malignancies
Presenter: Robert Walsh
Session: Poster session 09
230TiP - Exploring mechanisms of action and resistance in innovate cancer therapies: The UNLOCK program
Presenter: Beatriz Alonso de Castro
Session: Poster session 09
694P - Sequential high-dose-chemotherapy with 4 cycles paclitaxel, ifosfamide, carboplatin, etoposide (P-ICE) in relapsed/refractory male germ cell cancer: Final results with 15.8 years follow-up
Presenter: Hans Joachim Schmoll
Session: Poster session 09
695P - Assessment of the utility of CT scans in the long-term follow-up of metastatic non-seminomatous germ cell tumours (mNSGCT): The Late CT study
Presenter: Deep Chakrabarti
Session: Poster session 09
696P - Post chemotherapy retroperitoneal lymph node dissection (PC-RPLND) for metastatic pure seminoma
Presenter: David Pfister
Session: Poster session 09