Characteristics and Trends of Adult Acute Lymphoblastic Leukemia in a Large, Public Safety-Net Hospital

被引:5
作者
Gupta, Rohan [1 ,3 ]
Othman, Tamer [2 ]
Uche, An [1 ]
Amanam, Idoroenyi [1 ,3 ]
Chen, Chen [4 ]
Celles, Larissa [1 ]
Lane, Gregorianna [1 ]
Mei, Matthew [3 ]
Aldoss, Ibrahim [3 ]
Pullarkat, Vinod [3 ]
Kim, Phyllis [1 ]
Yeh, James [1 ]
机构
[1] Harbor UCLA Med Ctr, Div Hematol & Med Oncol, Torrance, CA 90509 USA
[2] Harbor UCLA Med Ctr, Dept Internal Med, Torrance, CA 90509 USA
[3] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplant, 1500 E Duarte Rd, Duarte, CA 91010 USA
[4] City Hope Canc Ctr, Ctr Informat, Duarte, CA USA
关键词
Acute lymphoblastic leukemia; Hematopoietic cell transplant; Insurance; Philadelphia chromosome; Underserved population; MINIMAL RESIDUAL DISEASE; CONSOLIDATION; ADOLESCENTS; THERAPY; REGIMEN; CANCER;
D O I
10.1016/j.clml.2019.11.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of adult acute lymphoblastic leukemia in the safety-net hospital setting has been heterogeneous given the lack of standardized guidelines. We retrospectively analyzed the outcomes of 90 patients with acute lymphoblastic leukemia treated at Harbor-UCLA Medical Center, a public hospital in Los Angeles County that lacks the capacity for therapeutic clinical trials and stem cell transplantation. Referral of patients with high-risk features to a transplant center may lead to improved survival. Background: Management of acute lymphoblastic leukemia (ALL) in a socioeconomically vulnerable population without ready access to a hematopoietic stem cell transplant (HCT) center and clinical trials is challenging. Data regarding the outcomes of such patients are sparse. Patients and Methods: This retrospective analysis included 90 consecutive patients with ALL who presented to Harbor-UCLA between 2003 and 2018. The primary objective was overall survival (OS), whereas secondary objectives included leukemia-free survival, toxicities of therapy, and referral for HCT and incidence of successful HCT. Results: Most patients were male (56.7%) and Hispanic (72.2%). The median age of diagnosis was 36 years (range, 18-63 years). The median OS was 26.8 months (95% confidence interval [CI], 17.4-59.0 months). In patients who achieved complete remission with therapy, the median leukemia-free survival was 16.4 months. Fifty percent of patients experienced at least 1 episode of bacteremia, and nearly 25% of patients developed an invasive fungal infection. Thirty-six percent (n = 32) of patients were referred for HCT. The referral rate increased over time, which led to improved OS in patients who underwent evaluation at a tertiary cancer center (hazard ratio, 0.44; 95% CI, 0.21-0.89; P=.02). Patients who underwent HCT had significantly better OS compared with those who did not (OS not reached vs. 21.9 months; hazard ratio, 0.16; 95% CI, 0.04-0.68; P=.01). Conclusion: Risk stratification and evidence-based treatment approaches are important for patients with ALL treated in a resource-limited setting. Most patients can be induced successfully and achieve complete remission with therapy. Partnership with a cancer center with early referral for HCT can facilitate curative HCT to be performed. Published by Elsevier Inc.
引用
收藏
页码:E320 / E327
页数:8
相关论文
共 23 条
[1]   Indications for allogeneic hematopoietic cell transplantation for adults with Philadelphia-chromosome negative acute lymphoblastic leukemia in first complete remission: all about MRD? [J].
Aldoss, Ibrahim ;
Pullarkat, Vinod .
BONE MARROW TRANSPLANTATION, 2019, 54 (01) :3-5
[2]   Trends in management of acute lymphoblastic leukemia: Influence of insurance based healthcare and treatment compliance on the outcome of adolescents and adults with acute lymphoblastic leukemia [J].
Arigela, Ravi Sankar ;
Gundeti, Sadashivudu ;
Ganta, Ranga Raman ;
Nasaka, Srividhya ;
Linga, Vijay Gandhi ;
Maddali, Lakshmi Srinivas .
INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2016, 37 (01) :32-37
[3]   Clinical significance of minimal residual disease quantification in adult patients with standard-risk acute lymphoblastic leukemia [J].
Brüggemann, M ;
Raff, T ;
Flohr, T ;
Gökbuget, N ;
Nakao, M ;
Droese, J ;
Lüschen, S ;
Pott, C ;
Ritgen, M ;
Scheuring, U ;
Horst, HA ;
Thiel, E ;
Hoelzer, D ;
Bartram, CR ;
Kneba, M .
BLOOD, 2006, 107 (03) :1116-1123
[4]  
CORTES JE, 1995, CANCER-AM CANCER SOC, V76, P2393, DOI 10.1002/1097-0142(19951215)76:12<2393::AID-CNCR2820761203>3.0.CO
[5]  
2-P
[6]  
Douer D, 2009, BLOOD, V114, P1199
[7]   Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia [J].
Goekbuget, Nicola ;
Dombret, Herve ;
Bonifacio, Massimiliano ;
Reichle, Albrecht ;
Graux, Carlos ;
Faul, Christoph ;
Diedrich, Helmut ;
Topp, Max S. ;
Brueggemann, Monika ;
Horst, Heinz-August ;
Havelange, Violaine ;
Stieglmaier, Julia ;
Wessels, Hendrik ;
Haddad, Vincent ;
Benjamin, Jonathan E. ;
Zugmaier, Gerhard ;
Nagorsen, Dirk ;
Bargou, Ralf C. .
BLOOD, 2018, 131 (14) :1522-1531
[8]   Acute lymphoblastic leukaemia in adult patients: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Hoelzer, D. ;
Bassan, R. ;
Dombret, H. ;
Fielding, A. ;
Ribera, J. M. ;
Buske, C. .
ANNALS OF ONCOLOGY, 2016, 27 :v69-v82
[9]   New insights into the pathophysiology and therapy of adult acute lymphoblastic leukemia [J].
Jabbour, Elias ;
O'Brien, Susan ;
Konopleva, Marina ;
Kantarjian, Hagop .
CANCER, 2015, 121 (15) :2517-2528
[10]   Ph-like acute lymphoblastic leukemia: a high-risk subtype in adults [J].
Jain, Nitin ;
Roberts, Kathryn G. ;
Jabbour, Elias ;
Patel, Keyur ;
Eterovic, Agda Karina ;
Chen, Ken ;
Zweidler-McKay, Patrick ;
Lu, Xinyan ;
Fawcett, Gloria ;
Wang, Sa A. ;
Konoplev, Sergej ;
Harvey, Richard C. ;
Chen, I-Ming ;
Payne-Turner, Debbie ;
Valentine, Marcus ;
Thomas, Deborah ;
Garcia-Manero, Guillermo ;
Ravandi, Farhad ;
Cortes, Jorge ;
Kornblau, Steven ;
O'Brien, Susan ;
Pierce, Sherry ;
Jorgensen, Jeffrey ;
Shaw, Kenna R. Mills ;
Willman, Cheryl L. ;
Mullighan, Charles G. ;
Kantarjian, Hagop ;
Konopleva, Marina .
BLOOD, 2017, 129 (05) :572-581