Abstract 706P
Background
NSGCTs with BMs are deemed poor-risk by definition. The data on the use and clinical outcomes of SRS in this cohort of patients (pts) is limited.
Methods
This retrospective audit included all pts with BM from metastatic NSGCT treated with SRS at the Royal Marsden Hospital between 2016 and 2024. Pts were required to meet the commissioning criteria for SRS (controllable/absent extracranial disease, expected prognosis ≥6 months, Karnofsy Performance Status, KPS >70). All pts were discussed in specialist germ cell and SRS MDMs. All were treated using a CyberKnife system.
Results
Ten pts were treated. One received 2 and another 3 courses of SRS; total no. of treatments delivered was 13. Median (IQR) age at diagnosis: 31.5 (22-46) yrs. Median (range) time to SRS from diagnosis: 8 (4-205) mts. 2/10 had mediastinal GCT, 8/10 had testicular GCT. 4/10 had BMs on diagnosis. Median (range) KPS: 90 (70-100). Most common chemotherapy regimens: high-dose stem cell rescue (6/10), TIP (5/10), IPE (4/10), CBOP-BEP (4/10). SRS treatments were: alone (9/13), boost post whole brain radiotherapy, WBRT (2/13), to tumour bed alone post-surgery (2/13). 4/10 pts had WBRT: 3/4 prior to SRS of whom 2/3 received SRS boost, 1/3 received SRS on progression; 1/4 had WBRT after debulking surgery on progression after SRS. Most had 1 BM on planning MRI (6/13). Mean (range) GTV/CTV volume: 4.24 (0.07-15.42) cc. SRS doses: 24Gy/3# (4/13), 24Gy/1# (3/13), 21Gy/1# (3/13), 20Gy/1# (1/13), 18Gy/3# (1/13), 18Gy/1# (1/13). Survival was analysed from date of SRS. Median (range) follow-up: 17 (1-80) mts. There were six instances of intracranial progression in 4/10 pts, all failed extracranially. 7/10 pts progressed extracranially: 1/7 salvaged, 3/7 died, 3/7 are on chemotherapy. Intracranial control: 6/10 pts. Both intracranial and extracranial control: 3/10 pts. Median (95% CI) progression-free survival (PFS): 4 (3-5) months. Mean (95% CI) overall survival (OS): 56 (34-78) mts. Two-year OS and PFS were 67% and 23%. The presence of a mediastinal primary adversely impacted OS (Mantel-Cox P=0.005). Younger age (<40 yrs) or BM at diagnosis did not affect OS or PFS.
Conclusions
The use of SRS achieved durable intracranial control in BM in mNSGCT and is appropriate in carefully selected patients.
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
836P - A prospective study to evaluate the prognostic implications and molecular mechanism of SLC40A1 gene in primary acute myeloid leukemia
Presenter: Harsh Goel
Session: Poster session 09
Resources:
Abstract
837P - Expression analysis, clinical significance and potential function of ALOX5AP in acute myeloid leukemia
Presenter: Harsh Goel
Session: Poster session 09
Resources:
Abstract
838P - Bayesian modeling in the survival analysis of patients with multiple myeloma with emphasis on missing data analysis
Presenter: Nelson Cruz Gutierrez
Session: Poster session 09
839P - Preliminary results from a phase II study of amulirafusp alfa (IMM0306) in patients with relapsed or refractory CD20-positive B-cell non-Hodgkin's lymphoma
Presenter: jianliang yang
Session: Poster session 09
840P - Orelabrutinib-based regimens in chronic lymphocytic leukemia with comorbidities: A real-world study
Presenter: Xun Lai
Session: Poster session 09
841P - Transforming the landscape of pediatric AML treatment: A cutting-edge SCT prognostic model
Presenter: Hua Yang
Session: Poster session 09
Resources:
Abstract
842P - Exploring the association of side-effects with depression in patients with chronic lymphocytic leukemia who have received treatment: An analysis of the lymphoma coalition’s 2022 global patient survey
Presenter: Natacha Bolanos Fernandez
Session: Poster session 09
843P - Challenges and insights in treating Langerhans cell histiocytosis: Persistent mutations and novel therapeutic approaches
Presenter: Marzieh NASHVI
Session: Poster session 09
844TiP - Orelabrutinib combined with rituximab for the treatment of elderly patients with newly diagnosed non-GCB diffuse large B-cell lymphoma (DLBCL) under the guidance of genetic subtype: A prospective, multicenter, single-arm, response-adaptive clinical study (Origin)
Presenter: Wanzhuo Xie
Session: Poster session 09
845TiP - CNS lymphoma imaging and molecular biomarkers study: CLIMB
Presenter: Panagiotis Ntellas
Session: Poster session 09