81 FDG-PET Interpreted By Deauville Criteria Prior to Allogeneic Transplantation Predicts Outcomes in Patients with Relapsed or Refractory Hodgkin Lymphoma

Track: BMT Tandem "Scientific" Meeting
Saturday, February 14, 2015, 4:45 PM-6:45 PM
Harbor Ballroom ABC (Manchester Grand Hyatt)
Aleksandr Lazaryan, MD MPH PhD , University of Minnesota Medical Center, Minneapolis, MN
Linda J. Burns, MD , National Marrow Donor Program, Minneapolis, MN
Qing Cao, MS , Biostatistics and Bioinformatics, University of Minnesota, Minneapolis, MN
Kaan Meric, MD , Radiology, Haydarpasa Numune Education and Research Hospital, Istanbul,, Turkey
Claudio G. Brunstein, MD, PhD , University of Minnesota Medical Center, Minneapolis, MN
Brian Lee McClune, DO , Univ of Minnesota Div Hem/Onc Transplant, Minneapolis, MN
Mukta Arora, MD, MS , University of Minnesota Medical Center, Minneapolis, MN
Margaret L. MacMillan, MD, MSc, FRCPC , Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN
Jerry Froelich, MD , Department of Diagnostic Radiology, University of Minnesota, Minneapolis, MN
John E. Wagner, MD , Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN
Daniel J. Weisdorf, MD , University of Minnesota Medical Center, Minneapolis, MN
Veronika Bachanova, MD , University of Minnesota Medical Center, Minneapolis, MN

Background: Despite high curative rates with upfront therapy, 20-30% of patients (pts) with Hodgkin lymphoma (HL) experience disease relapse. Survival is further diminished for those who fail autologous stem cell transplantation (ASCT). However a fraction of pts can still be salvaged with allogeneic hematopoietic cell transplantation (allo-HCT).

Methods: In this retrospective cohort study, we investigated the prognostic significance of FDG-PET (interpreted by both standard and Deauville criteria) among 42 consecutive patients with relapsed/refractory (RR) HL undergoing allo-HCT from 2004-2012. All FDG-PET scans were obtained within 4 weeks prior to allo-HCT. The study cohort included recipients of non-myeloablative (NMA) conditioning consisting of fludarabine 150-200 mg/m2, cyclophosphamide 50 mg/kg and total body irradiation TBI 200 cGy followed by transplantation of umbilical cord blood (n=30; 71%), matched related (n=10; 24%) and unrelated (n=2; 5%) donor grafts.

Results: The median age was 28 years (range, 6-59); 52% were males. Median time from HL diagnosis to allo-HCT was 34.6 months (range, 13.3-228.6) and median follow up of pts was 26.5 months (range, 0.8-97.1). Pts had received a median of 4 lines (range, 3-9) of prior regimens with 83% failing ASCT; only 13 pts (31%) had achieved PET-negative (neg) CR prior to allografting. Blinded re-evaluation of all pre-HCT FDG-PET scans using Deauville 5-point scale (i.e. PETD-pos if Deauville>3) by independent nuclear medicine physicians, confirmed all pre-existing PET-neg reports, but also reclassified 4 prior PET-pos scans as PETD-neg (kappa coefficient=0.79 [95% CI, 0.61-0.98] for PETD vs. archived PET). All 17 PETD-neg pts had significantly better 3-yr post-transplant OS, PFS, and relapse rate as compared to PETD-pos pts (100% vs. 51%; 76% vs. 17%; 24% vs. 65%, respectively; all p<0.01, Figure). Three out of four reclassified PETD-neg pts remained alive and in remission after a median follow up of 3.3 years (range, 1.0-8.0). Three-year non-relapse mortality for all pts was 7% (0% for PETD-neg vs. 12% for PETD-pos, p=0.1). Pre-HCT PETD-neg status remained prognostic for improved 3-yr OS (HR=0.1; 95% CI, 0-0.86) and lower relapse risk (HR=0.34; 95% CI, 0.1-1.0) in the multivariable Cox models.

Conclusions: Our study demonstrates encouraging outcomes achieved with NMA allo-HCT in heavily pre-treated pts (3-yr OS, PFS and relapse of 72% [95% CI, 54%-84%], 40% [95% CI, 24%-55%], 48% [95% CI, 29%-66%], respectively). FDG-PET imaging interpreted by Deauville criteria can serve as a powerful prognostic tool in pts with RR HL considered for NMA allo-HCT.

 

Disclosures:
A. Lazaryan, Millenium, Consultant: Advisory Board
GlyPharma, Member of the Scientific Advisory Board: Advisory Board
Alexion, Consultant: Consultancy
Seattle Genetics, Member of the Advisory Board: Advisory Board
Therakos, Consultant: Consultancy

M. Arora, Neovii Biotceh, External reviewer in a clinical trial: External reviewer

D. J. Weisdorf, Alexion, Consultant, data sharing: Consultancy and Research Funding
Amgen, Consultant: Consultancy
Pharmacyclics, Consultant, study planning: Consultancy
Enlivez, Study planning: Consultancy
Therakos, Speaking/Teaching: Educational lecture
Millenium, Consultation: Consultancy

V. Bachanova, Spectrum , consultant : Advisory Board
Seattle Genetics, advisory board : Advisory Board
Janssen, advisory board: Advisory Board