TY - JOUR
T1 - Use of foscarnet for cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation from a related donor
AU - Asakura, Maiko
AU - Ikegame, Kazuhiro
AU - Yoshihara, Satoshi
AU - Taniguchi, Shuichi
AU - Mori, Takehiko
AU - Etoh, Tetsuya
AU - Takami, Akiyoshi
AU - Yoshida, Takashi
AU - Fukuda, Takahiro
AU - Hatanaka, Kazuo
AU - Kanamori, Heiwa
AU - Yujiri, Toshiaki
AU - Atsuta, Yoshiko
AU - Sakamaki, Hisashi
AU - Suzuki, Ritsuro
AU - Ogawa, Hiroyasu
N1 - Funding Information:
Acknowledgments This work was supported in part by Health and Labour Sciences Research Grants for Clinical Cancer Research from the Ministry of Health, Labour, and Welfare, Japan. The authors would like to thank the staff of the Data Center of the Japan Society for Hematopoietic Cell Transplantation and the following collaborating institutions for providing patient data and specimens: Hokkaido University; Sapporo Hokuyu Hospital; Asahikawa Medical College; Hakodate Municipal Hospital; Aomori Prefectural Central Hospital; Tohoku University; Akita University; Kita-Fukushima Medical Center; Tsukuba University; Gunma University; Saitama Medical University International Medical Center; Matsudo Municipal Hospital; National Cancer Center Hospital; Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital; Jikei University; Keio University; Tokyo Women’s Medical University; Teikyo University; NTT Kanto Medical Center; Toranomon Hospital; Tokyo Medical and Dental University; National Hospital Organization Tokyo Medical Center; Yokohama City University; Kanagawa Cancer Center; Yokohama City University Medical Center; St. Marianna University; St. Marianna University Yokohama City Seibu Hospital; Niigata University; Niigata Cancer Center; Nagaoka Red Cross Hospital; Toyama Prefectural Central Hospital; Kanazawa University; Shinshu University; Gifu University; Hamamatsu Medical University; Meitetsu Hospital; Nagoya City University; Social insurance Chukyo
PY - 2010/9
Y1 - 2010/9
N2 - Foscarnet is an active agent against cytomegalovirus (CMV) infection after hematopoietic stem cell transplantation (HSCT), as well as ganciclovir. We investigated the usefulness of foscarnet in patients who underwent related allogeneic HSCT. Foscarnet was used in 320 patients with a median age of 45 years (range 15-72). The purpose of administration was CMV disease in 65, preemptive use in 248 and prophylaxis in 7. Totally, 194 patients had a history of prior ganciclovir treatment. The reason for foscarnet use was insufficient therapeutic effect of prior ganciclovir in 99, and adverse event including myelosuppression in 95. The response rate in symptom was 52% for the CMV disease patients. Antigenemia disappeared in 77% of the preemptive treatment and improved in 13% of the patients. No outbreak of CMV disease was recognized. The total effectiveness of therapeutic and preemptive use was significantly higher for patients without prior ganciclovir (91 vs. 76%, P = 0.001). Adverse events of grade 3 or higher were recognized in 24%, including electrolyte abnormalities in 11%, neutropenia in 8%, and thrombocytopenia in 8%. Renal damage was only observed in 3% of patients. Foscarnet was concluded to be a safe and effective anti-CMV agent and to be a suitable alternative to ganciclovir.
AB - Foscarnet is an active agent against cytomegalovirus (CMV) infection after hematopoietic stem cell transplantation (HSCT), as well as ganciclovir. We investigated the usefulness of foscarnet in patients who underwent related allogeneic HSCT. Foscarnet was used in 320 patients with a median age of 45 years (range 15-72). The purpose of administration was CMV disease in 65, preemptive use in 248 and prophylaxis in 7. Totally, 194 patients had a history of prior ganciclovir treatment. The reason for foscarnet use was insufficient therapeutic effect of prior ganciclovir in 99, and adverse event including myelosuppression in 95. The response rate in symptom was 52% for the CMV disease patients. Antigenemia disappeared in 77% of the preemptive treatment and improved in 13% of the patients. No outbreak of CMV disease was recognized. The total effectiveness of therapeutic and preemptive use was significantly higher for patients without prior ganciclovir (91 vs. 76%, P = 0.001). Adverse events of grade 3 or higher were recognized in 24%, including electrolyte abnormalities in 11%, neutropenia in 8%, and thrombocytopenia in 8%. Renal damage was only observed in 3% of patients. Foscarnet was concluded to be a safe and effective anti-CMV agent and to be a suitable alternative to ganciclovir.
KW - Adverse reaction
KW - Blood and marrow transplantation
KW - Cytomegalovirus infection
KW - Efficacy
KW - Foscarnet
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UR - http://www.scopus.com/inward/citedby.url?scp=77956931012&partnerID=8YFLogxK
U2 - 10.1007/s12185-010-0657-y
DO - 10.1007/s12185-010-0657-y
M3 - Article
C2 - 20694532
AN - SCOPUS:77956931012
SN - 0925-5710
VL - 92
SP - 351
EP - 359
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 2
ER -