How I treat immune thrombocytopenia: the choice between splenectomy or a medical therapy as a second-line treatment

被引:154
作者
Ghanima, Waleed [1 ,2 ]
Godeau, Bertrand [3 ]
Cines, Douglas B. [4 ,5 ]
Bussel, James B. [1 ]
机构
[1] Weill Cornell Med Coll, Dept Pediat Hematol Oncol, New York, NY 10065 USA
[2] Ostfold Hosp Trust Fredrikstad, Dept Internal Med, Fredrikstad, Norway
[3] Henri Mondor Univ Hosp, AP HP, UPEC, Dept Internal Med, Creteil, France
[4] Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
POPULATION-BASED COHORT; LOW-DOSE RITUXIMAB; TERM-FOLLOW-UP; LAPAROSCOPIC SPLENECTOMY; ADULT PATIENTS; DOUBLE-BLIND; PURPURA; EFFICACY; SAFETY; ITP;
D O I
10.1182/blood-2011-12-309153
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The paradigm for managing primary immune thrombocytopenia (ITP) in adults has changed with the advent of rituximab and thrombopoietin receptor agonists (TPO-RAs) as options for second-line therapy. Splenectomy continues to provide the highest cure rate (60%-70% at 5+ years). Nonetheless, splenectomy is invasive, irreversible, associated with postoperative complications, and its outcome is currently unpredictable, leading some physicians and patients toward postponement and use of alternative approaches. An important predicament is the lack of studies comparing second-line options to splenectomy and to each other. Furthermore, some adults will improve spontaneously within 1-2 years. Rituximab has been given to more than 1 million patients worldwide, is generally well tolerated, and its short-term toxicity is acceptable. In adults with ITP, 40% of patients are complete responders at one year and 20% remain responders at 3-5 years. Newer approaches to using rituximab are under study. TPO-RAs induce platelet counts > 50 000/mu L in 60%-90% of adults with ITP, are well-tolerated, and show relatively little short-term toxicity. The fraction of TPO-RA-treated patients who will be treatment-free after 12-24 months of therapy is unknown but likely to be low. As each approach has advantages and disadvantages, treatment needs to be individualized, and patient participation in decision-making is paramount. (Blood. 2012;120(5):960-969)
引用
收藏
页码:960 / 969
页数:10
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