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4807 Health Related Quality of Life and Fatigue in Patients with Pyruvate Kinase Deficiency

Program: Oral and Poster Abstracts
Session: 903. Outcomes Research—Non-Malignant Hematology: Poster III
Hematology Disease Topics & Pathways:
Diseases, Anemias, Clinically relevant
Monday, December 3, 2018, 6:00 PM-8:00 PM
Hall GH (San Diego Convention Center)

Eduard J. Van Beers, MD, PhD1*, Kevin H. M. Kuo, MD, MSc, FRCPC2, D. Holmes Morton, MD3,4*, Wilma Barcellini, MD5*, Stefan W. Eber, MD6, Bertil Glader, MD7, Hassan M. Yaish, MD8, Satheesh Chonat, MD9, Nina Kollmar, MD10*, Jenny M. Despotovic, DO, MS11, Dagmar Pospisilova, Prof. MD, PhD12*, Christine M. Knoll, MD13, Janet L. Kwiatkowski, MD14, Yves D. Pastore, MD15, Alexis A. Thompson, MD, MPH16, Winfred Wang, MD17, Marcin W. Wlodarski, MD, PhD18,19, Peter E. Newburger, MD20, Yaddanapudi Ravindranath, MBBS21, Jennifer A. Rothman, MD22, Heng Wang, MD, PhD23*, Suzanne Holzhauer, MD, MSc24*, Vicky R. Breakey, BSc, MEd, FRCPC25, Madeleine M Verhovsek, MD, FRCPC 26, Joachim B. Kunz, MD27*, Sujit Sheth, MD28, Mukta Sharma, MD, MPH29, Melissa J. Rose, DO30, Heather A. Bradeen, MD31*, Melissa A. McNaull, MD32, Kathryn Addonizio, BA33*, David N Williams34* and Rachael F. Grace, MD35

1Universitair Medisch Centrum Utrecht, Utrecht, Netherlands
2University Health Network, Toronto, ON, Canada
3Central Pennsylvania Clinic for Special Children & Adults, Belleville, PA
4Lancaster General Hospital, Lancaster, PA
5UOC Ematologia, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy
6Technical University, Schwerpunktpraxis für Pädiatrische Hämatologie- Onkologieand Children’s Hospital, Munich, Germany
7Department of Pediatrics, Stanford University School of Medicine, Stanford, CA
8Primary Children's Hospital, University of Utah, Salt Lake City, UT
9Aflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA
10Klinikum Kassel GmbH, Kassel, Germany
11Texas Children's Hospital, Baylor College of Medicine, Houston, TX
12Palacky University and University Hospital Olomouc, Olomouc, Czech Republic
13Phoenix Children's Hospital, Phoenix, AZ
14Division of Hematology, Children’s Hospital of Philadelphia, Philadelphia, PA
15CHU Sainte-Justine, University of Montreal, Montreal, QC, Canada
16Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL
17St. Jude Children's Research Hospital, Memphis, TN
18Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany
19Hematology, St. Jude Children's Research Hospital, Memphis, TN
20University of Massachusetts Medical School, Worcester, MA
21Children’s Hospital of Michigan, Wayne State University School of Medicine, Detroit, MI
22Duke University Medical Center, Durham, NC
23DDC Clinic for Special Needs Children, Middlefield, OH
24Charite Hospital, Berlin, Germany
25McMaster Children's Hospital, Hamilton, ON, Canada
26McMaster University, Hamilton, ON, Canada
27Zentrum für Kinder-und Jugendmedizin, Heidelberg, Germany
28New York Presbyterian Hospital, Weill Cornell Medical College, New York, NY
29Children’s Mercy Hospital, Kansas City, MO
30Nationwide Children’s Hospital, The Ohio State University College of Medicine, Columbus, OH
31The University of Vermont Children’s Hospital, Burlington, VT
32University of Mississippi Medical Center, Jackson, MS
33Dana-Farber Boston Children's Cancer and Blood Disorders Center, Boston, MA
34Institutional Centers for Clinical and Translational Studies, Boston Children's Hospital, Boston, MA
35Harvard Medical School, Dana-Farber Boston Children's Cancer and Blood Disorders Center, Boston, MA

Background: Pyruvate Kinase (PK) deficiency is the most common enzyme defect of the glycolytic pathway causing hereditary non-spherocytic hemolytic anemia. Patients have a broad phenotypic spectrum, ranging from mild anemia to transfusion dependence, and there is wide variation in transfusion practices and decisions about splenectomy. No prior studies have reported on the use of validated health related quality of life (HRQoL) measures in this population.

Aim: To describe patient reported outcomes including general HRQoL and fatigue in adults with PK deficiency and the correlation with clinical and laboratory features.

Methods: Patients were enrolled on the PK Deficiency Natural History Study, a prospective 30 site international study. All patients had molecularly confirmed PK deficiency. Adults (n=132), ages ≥18 years, completed the EuroQol-5D (high index equivalent to better QoL), PROMIS Fatigue Short Form 7a (high scores equivalent to higher fatigue), and the Functional Assessment of Cancer Therapy-Anemia (FACT-An, high scores equivalent to less fatigue) surveys at enrollment and annually. Timing of administration was convenience based. Survey data were analyzed according to proprietary scoring guidelines. Tests of association were performed using Fisher’s exact test (categorical) and Wilcoxon rank sum test (continuous). Regular transfusions were defined as ≥6 transfusions in 12 months. Genotypes were grouped as two missense mutations (M/M), one missense/one non-missense (M/NM), or two non-missense mutations (NM/NM)); non-missense included deletions or other drastic variants. The minimal important difference (MID) for the FACT-An has been reported as 7 points (Cella et al, J Pain Symptom Manage 2002). P-values <0.05 were considered statistically significant.

Results: At enrollment, 128 adults completed the FACT-An with a median total score of 156 (IQR 122-190). Patients receiving regular transfusions reported significantly lower FACT-An scores than those who were not regularly transfused (median 129 vs 156, p=0.004) with significantly lower scores for physical, emotional, and functional well-being and anemia sub-scores (Table). This difference also surpassed the MID. However, non- regularly transfused patients with hemoglobin (Hb) <8 g/dl did not report significantly different scores than those with Hb≥ 8 g/dl (p=0.75). There were also no significant differences in FACT-An scores by splenectomy status or age. The FACT-An score differences were greater than the MID for patients with iron overload (ferritin >1000 ng/dL or chelation), higher number of lifetime transfusions, and two missense mutations. Females reported significantly lower scores than males (median 143 vs. 160, p=0.006) with significantly lower anemia sub-scores (p=0.0009). FACT-An surveys completed at the one year follow-up time point validated these findings.

EuroQol-5D scores (n=124) at enrollment were similar to the healthy population (median PK deficiency index score 0.88; healthy population index mean 0.88, Shaw et al, Medical Care 2005). No significant differences were found by Hb level, splenectomy status, transfusion status, or genotype group. The median PROMIS fatigue T score (n=66) was 52.1 (IQR 40.5-63.7). Similar to the FACT-An survey data, PROMIS fatigue scores were significantly worse in patients who were regularly transfused (67.0 vs 52.4, p=0.02). PROMIS fatigue scores were also significantly worse in patients ≥40 years old (p=0.05) and females (p=0.01).

Conclusions: Using the FACT-An and PROMIS Fatigue measures, patients with PK deficiency who are regularly transfused report significantly more fatigue and worse HRQoL compared with those who are not transfused. Important differences were also seen by iron status and mutation group using the FACT-An. Patients report similar fatigue levels regardless of Hb level, which suggests that symptoms, rather than Hb value alone, should be factored into clinical decision making. In contrast to anemia related HRQoL scores, overall HRQoL scores using validated generic measures in patients with PK deficiency show no differences compared with the healthy population, suggesting that disease-specific measures may better detect the effects of PK deficiency on HRQoL.

Disclosures: Van Beers: Agios Pharmaceuticals: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding. Glader: Agios Pharmaceuticals: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding. Chonat: Agios Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees. Despotovic: AmGen: Research Funding; Novartis: Research Funding; Sanofi: Consultancy. Kwiatkowski: bluebird bio: Consultancy, Honoraria, Research Funding; Agios Pharmaceuticals: Consultancy, Research Funding; Novartis: Research Funding; Apopharma: Research Funding; Terumo: Research Funding. Thompson: La Jolla Pharmaceutical: Research Funding; Celgene: Research Funding; Novartis: Research Funding; Biomarin: Research Funding; bluebird bio: Consultancy, Research Funding; Baxalta/Shire: Research Funding; Amgen: Research Funding. Newburger: X4 Pharmaceutics: Consultancy, Honoraria; TransCytos LLC: Consultancy; Janssen Research & Development, LLC: Consultancy, Honoraria. Ravindranath: AGIOS: Other: Site Investigator for Pyruvate Kinase Deficiency. Sheth: Terumo Corporation: Research Funding; Novartis: Research Funding; La Jolla Pharmaceutical Company: Research Funding; Celgene Corporation: Consultancy, Research Funding; Bluebird Bio: Consultancy. Grace: Agios Pharmaceuticals: Consultancy; Agios Pharmaceuticals: Research Funding; Agios Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees.

*signifies non-member of ASH