Inhibitors against factor VIII in patients with cancer - Analysis of 41 patients

Authors
Citation
S. Sallah et Jy. Wan, Inhibitors against factor VIII in patients with cancer - Analysis of 41 patients, CANCER, 91(6), 2001, pp. 1067-1074
Citations number
37
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER
ISSN journal
0008543X → ACNP
Volume
91
Issue
6
Year of publication
2001
Pages
1067 - 1074
Database
ISI
SICI code
0008-543X(20010315)91:6<1067:IAFVIP>2.0.ZU;2-I
Abstract
BACKGROUND. The spontaneous formation of neutralizing antibodies (inhibitor s) to factor VIII (FVIII) in patients with cancer is a well known phenomeno n. However, to the authors' knowledge there is lack of information in the l iterature with respect to the clinical course of these patients and the nat ure of the association between malignant tumors and acquired hemophilia. METHODS. A retrospective study of 41 patients with cancer and acquired hemo philia was conducted. The patients were identified through a MEDLINE search between 1974-2000. All patients had detailed clinical and laboratory infor mation available and descriptions of the course of the inhibitor in relatio n to cancer treatment. The patients were divided into two groups: responder s and nonresponders. The stage of the tumor, inhibitor titer, MII level, an d survival data were examined and compared between the two groups. RESULTS. A total of 63 hemorrhagic episodes were reported in 25 patients wi th solid tumors and 16 patients with hematologic malignancies. The median i nhibitor titer at the time of the diagnosis of acquired hemophilia was 14 B ethesda units (BU) (range, 1-435 BU). The complete response (CR) rate to tr eatment of the inhibitor was 70% and patients who achieved a CR were more l ikely to have early stage tumors (P = 0.0007) and a lower median inhibitor titer at the time of presentation compared with nonresponders (12 BU vs. 78 BU; P = 0.007). The overall survival was significantly higher in patients who achieved a CR compared with patients with a persistent inhibitor (75% v s. 17%; P = 0.0006). CONCLUSIONS. Although it remains an uncommon occurrence, the development of inhibitors to FVIII should be considered as a cause of bleeding in some pa tients with malignant diseases. Because of the high response rate and the i mpact of this type of hemorrhage on cancer patients, efforts should be dire cted toward immunosuppression of the inhibitor in a fashion similar to that used in other patients with acquired hemophilia. To our knowledge the link between malignancy and the formation of antibodies to FVIII is unclear; ho wever, it appears that treatment of cancer with chemotherapy or surgery may accelerate the eradication of the inhibitor in some patients. Long term pr ospective studies are needed to better assess the association between cance r and acquired hemophilia. Cancer 2001;91:1067-74. (C) 2001 American Cancer Society.