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2801 Risk Factors Associated with 30-Day Unplanned Readmissions for Adult Acute Lymphoblastic Leukemia (ALL)

Program: Oral and Poster Abstracts
Session: 612. Acute Lymphoblastic Leukemia: Clinical Studies: Poster III
Hematology Disease Topics & Pathways:
Leukemia, ALL, Diseases, Lymphoid Malignancies, Clinically relevant, Quality Improvement
Monday, December 7, 2020, 7:00 AM-3:30 PM

Veronica A Guerra, MD1, Yasmin Alwash, MD2, Yan Yuanqing, PhD3*, Jorge M. Ramos Perez, MD4*, Guillaume Richard-Carpentier, MD2, Ahmad S. Alotaibi, MD5*, Hycienth O Ahaneku, MD, MPH, PhD4, Bachar Samra, MD4*, Arrvind Raghunath, MD4*, Nitin Jain, MD6, Nicholas J. Short, MD4, Farhad Ravandi, MBBS4, Gautam Borthakur, MD4, Alessandra Ferrajoli, MD4, Koji Sasaki, MD2, Steven M. Kornblau, MD4, Zeev E. Estrov, MD4, Jorge E. Cortes, MD7, Hagop M. Kantarjian, MD4, Guillermo Garcia-Manero, MD4, Elias Jabbour, MD4 and Tapan M. Kadia, MD4

1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Miami, FL
2Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, TX
3University of Texas Health Science Center, Department of Neurosurgery, Houston
4Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
5Department of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX
6The University of Texas MD Anderson Cancer Center, Houston, TX
7Georgia Cancer Center Augusta University, Augusta, GA

Background Unplanned 30-day readmissions are a frequent complication of acute leukemia therapy. However, there is limited data in acute lymphoblastic leukemia (ALL), with reported readmission rates (RaR) of 36% for pediatric ALL.

Methods We retrospectively reviewed hospitalizations for ALL for adult patients >/= 18 years at our institution between January 2018 and December 2018. Unplanned readmissions were defined as any hospitalization within 30-days after discharge from the index admission, excluding all elective re-admissions for scheduled chemotherapy. Patients >/= 55 years of age receiving their initial induction therapy remained hospitalized for at least 21 days until bone marrow analysis and neutrophil count above 500/mm3.

The primary objective was to identify the 30-day unplanned readmission rates, cause of readmissions, and predicted factors for readmissions. The secondary outcome included 30-day readmission mortality rate and inpatient mortality rate.

Results There were a total of 841 ALL hospitalizations, 94 admissions for 63 pts (average 1.49 re-admit/pt) during frontline induction, 443 for 123 pts (average 3.6) during consolidation and 304 for 92 pts (average 3.3) with relapsed/refractory ALL (R/R ALL). The median age was 43 years for the frontline induction, 45 years for the consolidation group, and 42 years for R/R ALL patients. Baseline characteristics are listed in Table 1. The median length of index admission was 11 days for induction, 4 days during consolidation, and 8 days for R/R ALL. The 30-day unplanned RaR was 32% for induction, 28% for consolidation, and 36% for R/R ALL, with a median time to readmission of 6 days, 6 days, and 5 days, respectively.

The most common causes of readmissions were infections (60%, 60% and 29% during induction, consolidation and R/R ALL respectively), including 30% neutropenic fever of unknown origin (NF), pain 20%, gastrointestinal infections 13%, neurologic causes (altered mental status, headache and LE weakness) 13%, and 10% bacteremia for induction; 19% neurologic causes, 17% NF, 15% upper respiratory infections, and11% pain during consolidation; and 9% bleeding, 8% NF, and 6% bacteremia for R/R ALL. (Figure 1)

The median length of readmission was 5 days, 4 days, and 7 days for induction, consolidation, and R/R ALL patients, with a rate of ICU stay of 7%, 2%, and 18%, respectively. (Figure 2)

While no significant differences were seen in the rate of ICU stay between readmissions and non-readmission for the induction and consolidation groups, R/R ALL patients had an increased incidence of ICU stay (18% vs. 11%, p=.001) and 30-day mortality (13% vs. 5% p=.010).

We performed a logistical regression analysis to determine risk factors associated with readmissions. The multivariate analysis identified COPD (OR 3.30, p=.016) as an independent predictor for readmissions and male sex was associated with a decreased risk (OR 0.58, p=.016) during consolidation therapy; meanwhile, Philadelphia positive ALL (Ph+ALL) was negatively associated with RaR for R/R ALL pts (OR 0.33, p=.014). (Table 2) There was no significant association between the commonly used L.A.C.E. score and the risk of readmissions among consolidation and R/R ALL pts. However, during induction, a higher L.A.C.E score was negatively associated with the risk of readmission (OR 0.30, p=.027), likely due to a longer duration of hospital stay for high-risk patients (18 days vs. 8 days, p=.000).

The 30-day mortality rate and inpatient mortality rate was 3% for unplanned induction readmissions, 0% for consolidation, and 13% for R/R ALL. One patient (3%) died after readmission during induction due to infection. The 30-day mortality rate after readmission for R/R ALL patients was 13%, with 50% of deaths due to infections and 30% due to disease progression.

Conclusions Unplanned 30-day readmissions were frequent among patients with ALL, with similar rates between each sequential line of therapy, and the most common cause was infections. The 30-day mortality remains low for induction and consolidation pts, with a significantly higher risk for ICU stay and 30-day mortality for R/R ALL pts. We identified COPD, female sex, and non-Ph+ ALL as independent predictors for readmission. However, the majority of the pts were younger, with only 24-34% above 55 years of age. Implementing more frequent monitoring and increased precautions in high-risk pts could help reduce mortality in ALL.

Disclosures: Jain: Aprea Therapeutics: Research Funding; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees; ADC Therapeutics: Research Funding; Precision Bioscienes: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Incyte: Research Funding; Adaptive Biotechnologies: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; TG Therapeutics: Honoraria, Membership on an entity's Board of Directors or advisory committees; AbbVie: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Cellectis: Research Funding; Fate Therapeutics: Research Funding; AstraZeneca: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Genentech: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Pharmacyclics: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Verastem: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Servier: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; BeiGene: Honoraria, Membership on an entity's Board of Directors or advisory committees; BMS: Research Funding; Pfizer: Research Funding. Short: AstraZeneca: Consultancy; Astellas: Research Funding; Amgen: Honoraria; Takeda Oncology: Consultancy, Honoraria, Research Funding. Ravandi: Celgene: Consultancy, Honoraria; Orsenix: Consultancy, Honoraria, Research Funding; Abbvie: Consultancy, Honoraria, Research Funding; BMS: Consultancy, Honoraria, Research Funding; Amgen: Consultancy, Honoraria, Research Funding; Astellas: Consultancy, Honoraria, Research Funding; Macrogenics: Research Funding; Xencor: Consultancy, Honoraria, Research Funding; AstraZeneca: Consultancy, Honoraria; Jazz Pharmaceuticals: Consultancy, Honoraria, Research Funding. Borthakur: Abbvie: Research Funding; Curio Science LLC: Consultancy; Polaris: Research Funding; Jannsen: Research Funding; PTC Therapeutics: Consultancy; Argenx: Consultancy; PTC Therapeutics: Research Funding; GSK: Research Funding; FTC Therapeutics: Consultancy; Treadwell Therapeutics: Consultancy; BMS: Research Funding; AstraZeneca: Research Funding; Novartis: Research Funding; Incyte: Research Funding; Cyclacel: Research Funding; BioLine Rx: Consultancy; Xbiotech USA: Research Funding; BioLine Rx: Research Funding; Oncoceutics: Research Funding; BioTherix: Consultancy; Nkarta Therapeutics: Consultancy. Sasaki: Otsuka: Honoraria; Pfizer Japan: Consultancy; Novartis: Consultancy, Research Funding; Daiichi Sankyo: Consultancy. Cortes: Takeda: Consultancy, Research Funding; Sun Pharma: Research Funding; Merus: Research Funding; Astellas: Research Funding; Telios: Research Funding; BiolineRx: Consultancy, Research Funding; Arog: Research Funding; Amphivena Therapeutics: Research Funding; Jazz Pharmaceuticals: Consultancy, Research Funding; Daiichi Sankyo: Consultancy, Research Funding; Bristol-Myers Squibb: Research Funding; BioPath Holdings: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Immunogen: Research Funding; Pfizer: Consultancy, Research Funding; Novartis: Consultancy, Research Funding. Kantarjian: Actinium: Honoraria, Membership on an entity's Board of Directors or advisory committees; Agios: Honoraria, Research Funding; Ariad: Research Funding; Amgen: Honoraria, Research Funding; Takeda: Honoraria; AbbVie: Honoraria, Research Funding; BMS: Research Funding; Novartis: Research Funding; Astex: Research Funding; Daiichi-Sankyo: Research Funding; Immunogen: Research Funding; Pfizer: Honoraria, Research Funding; Cyclacel: Research Funding; Jazz Pharma: Research Funding. Garcia-Manero: AbbVie: Honoraria, Research Funding; Acceleron Pharmaceuticals: Consultancy, Honoraria; Celgene: Consultancy, Honoraria, Research Funding; Helsinn Therapeutics: Consultancy, Honoraria, Research Funding; Novartis: Research Funding; Merck: Research Funding; Astex Pharmaceuticals: Consultancy, Honoraria, Research Funding; Jazz Pharmaceuticals: Consultancy; Bristol-Myers Squibb: Consultancy, Research Funding; Genentech: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Onconova: Research Funding; H3 Biomedicine: Research Funding; Amphivena Therapeutics: Research Funding. Jabbour: AbbVie: Other: Advisory role, Research Funding; Pfizer: Other: Advisory role, Research Funding; BMS: Other: Advisory role, Research Funding; Amgen: Other: Advisory role, Research Funding; Genentech: Other: Advisory role, Research Funding; Takeda: Other: Advisory role, Research Funding; Adaptive Biotechnologies: Other: Advisory role, Research Funding. Kadia: Incyte: Research Funding; Celgene: Research Funding; Cellenkos: Research Funding; Genentech: Honoraria, Research Funding; JAZZ: Honoraria, Research Funding; Cyclacel: Research Funding; Novartis: Honoraria; Pulmotec: Research Funding; Abbvie: Honoraria, Research Funding; Ascentage: Research Funding; Astra Zeneca: Research Funding; Amgen: Research Funding; Pfizer: Honoraria, Research Funding; BMS: Honoraria, Research Funding; Astellas: Research Funding.

*signifies non-member of ASH