104 Risk Factors Predicting Outcomes of Autologous Hematopoietic Cell Transplantation (autoHCT) in Children, Adolescents and Young Adults (CAYA) with Relapsed/Refractory (Rel/Ref) Classical Hodgkin Lymphoma (HL): A CIBMTR Analysis

Track: BMT Tandem "Scientific" Meeting
Friday, February 13, 2015, 10:30 AM-12:00 PM
Seaport Ballroom ABC (Manchester Grand Hyatt)
Prakash Satwani, MD , Division of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Department of Pediatrics, Columbia University Medical Center, New York, NY
Kwang Woo Ahn, PhD , Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI
Jeanette Carreras, MPH , CIBMTR, Medical College of Wisconsin, Milwaukee, WI
David G. Maloney, MD, PhD , Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA
Anna Sureda, MD , Institut Catalā d'Oncologia, Hospital Duran i Reynals, Barcelona, Spain
Sonali M. Smith, MD , University of Chicago, Chicago, IL
Mehdi Hamadani, MD , CIBMTR, Medical College of Wisconsin, Milwaukee, WI

Introduction: AutoHCT is a potentially curative modality for Rel/Ref HL. However, large studies evaluating the risk factors predicting outcomes of autoHCT in CAYA with Rel/Ref HL have not been performed.

Methods: CAYA (age <30yrs) with Rel/Ref classical HL undergoing autoHCT during 1995-2010 were eligible. HIV+ patients and those undergoing tandem HCT were excluded.

Results: Baseline characteristics of 671 CAYA included in the analysis are shown in Table. The 3yr non-relapse mortality (NRM), rate of relapse/progression (R/P), progression free survival (PFS) and overall survival (OS) were 6%, 38%, 56% and 73%, respectively. On multivariate analysis non-ABVD/ABVD-like 1st line therapy (RR 1.8; p=0.03) was associated with a higher NRM. Factors predicting higher risk of R/P included Lansky score (LS) or KPS<90 (RR 1.6; p=0.0006), extranodal disease (END) (RR 1.6; p=0.001), resistant disease (RR 1.8; p<0.0001) and CBV conditioning (RR 1.6; p=0.002). Long first complete remission (LgCR1; ≥1yr) was associated with a reduced R/P risk (RR 0.6; p=0.003). MVA for PFS identified END (RR 1.5; p=0.001), resistant disease (RR 1.9; p<0.0001) and KPS<90 (RR 1.5; p=0.0004) as risk factors for therapy failure; while LgCR1 (0.7; p=0.006) was predictive of reduced therapy failure risk. Finally for OS, non-ABVD/ABVD-like 1st line therapy (RR 1.5; p=0.001), END (RR 1.7; p=.0003) and resistant disease (RR 2.3; p<0.0001) were associated with higher mortality; while LgCR1 (RR 0.5; p=0.0006) and peripheral blood graft (RR 0.49, p=0.0001) were associated with reduced mortality risk. Age was not predictive of autoHCT outcomes.

Conclusions:  Unlike adult HL patients, age is not a prognostic factor for CAYA outcomes following autoHCT. In this largest CAYA study to date; LgCR1, LS/KPS, chemoresistance, END and non-ABVD/ABVD-like 1st line therapy emerge as factors predicting autoHCT survival outcomes in CAYA with HL. These data help identify potential high risk Rel/Ref CAYA with HL, where investigation of novel post autoHCT (maintenance, consolidation, immunomodulatory etc.) approaches is warranted.

 

Baseline characteristics

N=671 (%)

Median age (range)

23 (3-29)

<21 yrs

230 (34)

KPS ≥90

498 (74)

Duration of 1st CR

    <12mons (including primary refractory)

    ≥12mons

    Missing

361 (54)

237 (35)

73 (11)

Time from diagnosis to HCT, mons (range)

19 (3-238)

High LDH at HCT

174 (26)

Median lines of therapies (range)

2 (1-5)

ABVD or ABVD-like 1st line therapy

396 (59)

END at HCT

118 (18)

Bulky disease at HCT

77 (11)

Disease status at HCT

    Sensitive

    Resistant

    Missing

529 (79)

125 (19)

17 ( 3)

Radiation post HCT

205 (31)

Conditioning

    BEAM

    CBV

    Others

455 (68)

80 (12)

136 ( 20)

Graft type

    BM

    PB

65 (10)

606 (90)

Median follow-up, mons (range)

64 (4-216)

 


Disclosures:
Nothing To Disclose