Geer Marcus J, Foucar Charles E, Devata Sumana, Benitez Lydia, Perissinotti Anthony J, Marini Bernard L, Bixby Dale
1Division of Hematology and Medical Oncology, Department of Internal Medicine, Michigan Medicine and University of Michigan Medical School, Ann Arbor, Michigan.
2Division of Hematology and Medical Oncology, Department of Internal Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; and.
J Natl Compr Canc Netw. 2021 Aug 17;19(11):1272-1275. doi: 10.6004/jnccn.2021.7013.
All-trans retinoic acid (ATRA) serves as the backbone of the management of patients with acute promyelocytic leukemia (APL), with guidelines recommending the initiation of ATRA as soon as APL is suspected. As a regional referral center for patients with acute leukemia, those who are suspected of having APL are often transferred to our facility. However, many referring centers are unable to initiate treatment using ATRA. We conducted an exploratory analysis of the clinical availability of ATRA and the factors limiting access to this critical drug.
The United States was divided into 6 geographic regions: Northwest, Southwest, Central, Southeast, Northeast, and the Great Lakes. Twenty hospitals were randomly selected from states within each of these regions and were surveyed as to whether they typically treated patients with acute leukemia, the availability of ATRA at their institution, and reported reasons for not stocking ATRA (if not available).
Less than one-third of hospitals queried (31%) had ATRA in stock. Neither the size of the hospital nor the hospital's status as academic versus nonacademic (53% vs 31%; P=.08) influenced ATRA availability. Of the hospitals that referred patients with APL, only 14% (7/49) had ATRA readily available. Hospitals that treated patients with APL were more likely to have ATRA available than referring centers (58% vs 14%; P=.000002).
Nearly two-thirds of the hospitals surveyed that cared for patients with acute leukemia do not have ATRA immediately available. Moreover, the vast majority of hospitals that refer patients to other centers do not have ATRA. These findings should spur investigation into the impact of immediate ATRA availability on the morbidity and mortality of patients with APL. A call by hematologists nationwide to their formulary committees is warranted to ensure that this lifesaving medication is available to patients suspected of having APL.
全反式维甲酸(ATRA)是急性早幼粒细胞白血病(APL)患者治疗的基础药物,相关指南建议一旦怀疑为APL应尽快开始使用ATRA治疗。作为急性白血病患者的区域转诊中心,疑似患有APL的患者常被转至我院。然而,许多转诊中心无法使用ATRA开始治疗。我们对ATRA的临床可及性以及限制获取这种关键药物的因素进行了探索性分析。
美国被划分为6个地理区域:西北、西南、中部、东南、东北和五大湖地区。从这些区域内的各州随机选取20家医院,调查其是否通常治疗急性白血病患者、医院内ATRA的可及情况以及报告未储备ATRA的原因(若未储备)。
接受调查的医院中,不到三分之一(31%)储备有ATRA。医院规模以及医院是学术性还是非学术性(53%对31%;P = 0.08)均未影响ATRA的可及性。在转诊APL患者的医院中,只有14%(7/49)的医院有现成的ATRA。治疗APL患者的医院比转诊中心更有可能有ATRA可用(58%对14%;P = 0.000002)。
接受调查的近三分之二的诊治急性白血病患者的医院没有现成的ATRA。此外,绝大多数将患者转诊至其他中心的医院没有ATRA。这些发现应促使人们调查立即获得ATRA对APL患者发病率和死亡率的影响。有必要呼吁全国血液学家向其处方委员会施压,以确保疑似患有APL的患者能够获得这种救命药物。