This website and third-party tools we use rely on cookies for the best user experience. By selecting "I agree", you agree to cookie usage as described in our Privacy Policy.
1,267 posters, 47 videos, 13 topics, 4 sessions, 853 authors
ePostersLive by SciGen Technologies S.A. All rights reserved.
September 9 - 12, 2026 | George R. Brown Convention Center, Houston, Texas
HL - 215
Hodgkin Lymphoma (HL)
Autologous Stem Cell Transplantation for Relapsed/Refractory Hodgkin Lymphoma in a Resource-Limited Setting: A Real-World Study from Pakistan
Hammad Javed¹, Tariq Ghafoor¹, Nighat Shahbaz¹, Mehreen Ali Khan¹, Raheel Iftikhar¹, Jahanzeb Liaqat¹
¹Armed Forces Bone Marrow Transplant Center, Rawalpindi, Punjab, Pakistan
KEYWORDS: Hodgkin lymphoma, autologous stem cell transplantation, relapsed/refractory, low- and middle-income countries
CONTEXT:
Management of relapsed or refractory classical Hodgkin lymphoma (RR-cHL) remains challenging in low- and middle-income countries (LMICs) due to limited access to advanced diagnostic facilities and novel therapies. High-dose therapy (HDT) followed by autologous stem cell transplantation (ASCT) remains the standard of care for chemosensitive disease; however, real-world data from LMICs are limited.
OBJECTIVE:
To evaluate real-world outcomes of ASCT in patients with RR-cHL in a resource-limited setting and to identify prognostic factors associated with survival outcomes.
DESIGN:
Retrospective cohort study of consecutive patients with RR-cHL undergoing ASCT between January 2010 and December 2023, with survival analysis performed using the Kaplan–Meier method and Cox proportional hazards modeling.
SETTING:
Single tertiary care transplant center in Pakistan.
PATIENTS OR OTHER PARTICIPANTS:
A total of 60 consecutive patients with RR-cHL were included. Median age was 26 years (IQR, 16.1–32.3), and 66.7% were male. At diagnosis, 79% had advanced-stage disease and 63% had B symptoms. High-risk features included primary refractory disease (23.3%) and early relapse (41.6%).
INTERVENTIONS:
Patients received salvage chemotherapy, including novel agent–based regimens in 68.3% of cases, followed by high-dose therapy and ASCT. At the time of transplant, 85% of patients were in complete remission.
MAIN OUTCOMES MEASURES:
Primary endpoints were progression-free survival (PFS) and overall survival (OS). Secondary outcomes included relapse incidence and non-relapse mortality.
RESULTS:
At a median follow-up of 21.1 months, the estimated 2-year PFS was 80.9% (95% CI, 66.9–89.4) and OS was 85.8% (95% CI, 73.5–92.7). The 2-year cumulative incidence of relapse was 19.1%, and day +100 non-relapse mortality was 5%. On multivariable analysis, primary refractory disease was independently associated with inferior PFS (HR 4.89, P = .002) and OS (HR 4.21, P = .027).
CONCLUSIONS:
In this real-world LMIC setting, ASCT for RR-cHL is feasible and yields survival outcomes comparable to international benchmarks despite resource constraints. Achieving remission prior to transplantation remains a key determinant of outcomes. These findings support the continued role of ASCT and highlight the need to improve access to effective salvage therapies in resource-limited settings.