A multicenter phase 2 study of empirical low-dose liposomal amphotericin B in patients with refractory febrile neutropenia.

Kotaro Miyao, Masashi Sawa, Mio Kurata, Ritsuro Suzuki, Reona Sakemura, Toshiyasu Sakai, Tomonori Kato, Satomi Sahashi, Natsuko Tsushita, Yukiyasu Ozawa, Motohiro Tsuzuki, Akio Kohno, Tatsuya Adachi, Keisuke Watanabe, Kaneyuki Ohbayashi, Yuichiro Inagaki, Yoshiko Atsuta, Nobuhiko Emi

Journal: International journal of hematology 2017;105(1):79-86

PMID: 27696283

Abstract

Invasive fungal infection (IFI) is a major life-threatening problem encountered by patients with hematological malignancies receiving intensive chemotherapy. Empirical antifungal agents are therefore important. Despite the availability of antifungal agents for such situations, the optimal agents and administration methods remain unclear. We conducted a prospective phase 2 study of empirical 1 mg/kg/day liposomal amphotericin B (L-AMB) in 80 patients receiving intensive chemotherapy for hematological malignancies. All enrolled patients were high-risk and had recurrent prolonged febrile neutropenia despite having received broad-spectrum antibacterial therapy for at least 72 hours. Fifty-three patients (66.3 %) achieved the primary endpoint of successful treatment, thus exceeding the predefined threshold success rate. No patients developed IFI. The treatment completion rate was 73.8 %, and only two cases ceased treatment because of adverse events. The most frequent events were reversible electrolyte abnormalities. We consider low-dose L-AMB to provide comparable efficacy and improved safety and cost-effectiveness when compared with other empirical antifungal therapies. Additional large-scale randomized studies are needed to determine the clinical usefulness of L-AMB relative to other empirical antifungal therapies.

Address: Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan. [email protected].; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan. [email protected].; Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.; Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.; Center for Supporting Hematology-Oncology Trials, Nagoya, Japan.; Department of HSCT Data Management and Biostatistics, Nagoya University, Nagoya, Japan.; Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.; Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.; Department of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.; Department of Hematology, Fujita Health University, Toyoake, Japan.; Department of Hematology and Oncology, Konan Kosei Hospital, Konan, Japan.; Department of Hematology and Oncology, Chukyo Hospital, Nagoya, Japan.; Department of Hematology, Nishio Munishipal Hospital, Nishio, Japan.; Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.

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