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
697P - The Empower Pathway overview: An innovative approach to delivering personalised care for testicular cancer survivors
Presenter: Robert Holwell
Session: Poster session 09
698P - Outcomes of patients with testicular germ cell tumors in Latin-America
Presenter: Saul Campos Gomez
Session: Poster session 09
699P - Prospective COTRIMS (COlogne Trial of Retroperitoneal Lymphadectomy in Metastastic Seminoma) trial: Three year update
Presenter: Axel Heidenreich
Session: Poster session 09
701P - Multicenter analysis of first-line (1L) regimens (BEP vs VIP) in patients (pts) with non-seminomatous germ cell tumors (NSGCTs) who subsequently underwent high-dose chemotherapy (HDCT)
Presenter: Hedyeh Ebrahimi
Session: Poster session 09
702P - Survival and related factors in testicular non-seminomatous patients undergoing high-dose chemotherapy and autologous stem cell transplantation: Experience of Turkey's highest volume transplantation center
Presenter: Musa Baris Aykan
Session: Poster session 09
703P - Survival of Hispanic germ cell tumor patients at a single academic institution vs. SEER
Presenter: Adam Kolawa
Session: Poster session 09
704P - Characteristics and palliative management of patients with cisplatin-refractory germ cell tumours: A Global Germ Cell Cancer Collaborative Group (G3) retrospective registry study
Presenter: Christoph Oing
Session: Poster session 09
705P - Subsequent malignant neoplasms (SMN) in patients with germ cell tumor of the testis (TGCT): Implications on a genetic vs stem cell origin of cancers
Presenter: Sruthi Vellanki
Session: Poster session 09
706P - Stereotactic radiosurgery (SRS) in brain metastases (BMs) from non-seminomatous germ cell tumours (NSCGTs)
Presenter: Deep Chakrabarti
Session: Poster session 09