Klofarabin bazlı tedavi alan relaps veya refrakter akut lösemi tanılı hastaların retrospektif değerlendirilmesi
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Date
2021-06-15
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Bursa Uludağ Üniversitesi
Abstract
Relaps veya refrakter akut lösemide klofarabin bazlı kurtarma tedavilerinin genel yanıt oranları %17-48 arasında değişmektedir. Çalışmamızda relaps veya refrakter akut lösemi tanılı hastalarda klofarabin bazlı kurtarma tedavisi sonrası yanıt oranları, enfeksiyon ile ilişkili komplikasyonları ve yan etkileri değerlendirildi. Ocak 2015 ile Aralık 2020 tarihleri arasında kliniğimizde klofarabin bazlı kurtarma tedavisi alan 12 hasta retrospektif olarak değerlendirildi. Hastaların %58 (n=7)’i erkek olup ortalama yaş 36,6±16,4 olarak saptandı. Hastaların %75 (n=9)’i akut lenfoblastik lösemi, %25 (n=3)’i akut myeloid lösemi tanısı ile takip edilmekteydi. Klofarabin öncesi almış oldukları kemoterapi rejim sayısı medyan 3 idi. Hastaların %66 (n=8)’sı son aldığı tedaviye refrakter, %33 (n=4)’ü erken nüks ile başvurdu. Hastalar klofarabin 22,5 mg/m2 + sitozin arabinozid 1000 mg/m2 dozunda intravenöz 1-5. gün olacak şekilde tedavi aldılar. Tedavi esnasında tüm hastalar febril nötropeni ile komplike oldu, hastaların %58 (n=7)’inde sepsis gelişti. Ciddi (grade 3-4) non- hematolojik yan etkiler arasında hepatotoksisite %33, diyare %25, bulantı-kusma %16, mukozit %16 civarındaydı. Klofarabine bağlı nörotoksisite izlenmedi. Hastaların birinde tam yanıt (%8) elde edildi. Hastaların %33 (n=4)’ü tedaviye yanıtsızdı. İlk 30 gün içindeki mortalite oranı %50 (n=6) idi. Mortal seyreden hastaların bir tanesinde erken ölüm (<2 hafta) oldu. Refrakter veya erken nüks akut lösemi hastaları için esas amaç kurtarma tedavisi sonrası allojenik kemik iliği nakline ilerlemektir. Her ne kadar kemik iliği nakli ile kür sağlanabilse de 4 yıllık sağ kalım %25-30’u geçmemektedir. Dolayısıyla relaps veya refrakter akut lösemi hastalarında günümüzde halen güçlü ve etkili bir kurtarma tedavi rejimine ihtiyaç duyulmaktadır.
Overall response rates of clofarabine-based rescue regimens in relapsed or refractory acute leukemia range from 17-48%. In our study, response rates, infection-related complications and side effects were evaluated after salvage therapy with clofarabine-based regimens in patients diagnosed with relapsed and/or refractory acute leukemia. Twelve patients who received clofarabine-based rescue therapy in our clinic between January 2015 and December 2020 were evaluated retrospectively. Fifty-eight percent of the patients were male and the mean age was 36.6±16.4 years. Seventy-five percent of the patients had a diagnosis of acute lymphoblastic leukemia, 25% had a diagnosis of acute myeloid leukemia. A median of 3 cycles of chemotherapy was given before clofarabine. Sixty-six percent of the patients were followed as refractory to the last treatment, and 33% as early relapse. Patients received intravenous treatment between 1st and 5th days at a dose of clofarabine 22,5 mg/m2 +cytarabine 1000 mg/m2 . During the treatment, all patients were complicated with febrile neutropenia, 58% of them developed sepsis. Serious (grade 3-4) non-hematological side effects were hepatotoxicity in 33%, diarrhea in 25%, nausea and vomiting in 16%, and mucositis in 16%. Neurotoxicity related to clofarabine was not observed. One of the patients achieved complete response (8%), 33% of the patients were unresponsive. The mortality rate within the first 30 days was 50% (n = 6). Early death (<2 weeks) occurred in one of the severe patient. For patients with refractory or early relapse acute leukemia, the main goal is to progress to allogeneic bone marrow transplantation after salvage therapy. Although complete remission can be achieved with bone marrow transplantation, 4-year survival does not exceed 25-30%. Therefore, a powerful and effective salvage treatment regimen is still needed in patients with relapsed or refractory acute leukemia.
Overall response rates of clofarabine-based rescue regimens in relapsed or refractory acute leukemia range from 17-48%. In our study, response rates, infection-related complications and side effects were evaluated after salvage therapy with clofarabine-based regimens in patients diagnosed with relapsed and/or refractory acute leukemia. Twelve patients who received clofarabine-based rescue therapy in our clinic between January 2015 and December 2020 were evaluated retrospectively. Fifty-eight percent of the patients were male and the mean age was 36.6±16.4 years. Seventy-five percent of the patients had a diagnosis of acute lymphoblastic leukemia, 25% had a diagnosis of acute myeloid leukemia. A median of 3 cycles of chemotherapy was given before clofarabine. Sixty-six percent of the patients were followed as refractory to the last treatment, and 33% as early relapse. Patients received intravenous treatment between 1st and 5th days at a dose of clofarabine 22,5 mg/m2 +cytarabine 1000 mg/m2 . During the treatment, all patients were complicated with febrile neutropenia, 58% of them developed sepsis. Serious (grade 3-4) non-hematological side effects were hepatotoxicity in 33%, diarrhea in 25%, nausea and vomiting in 16%, and mucositis in 16%. Neurotoxicity related to clofarabine was not observed. One of the patients achieved complete response (8%), 33% of the patients were unresponsive. The mortality rate within the first 30 days was 50% (n = 6). Early death (<2 weeks) occurred in one of the severe patient. For patients with refractory or early relapse acute leukemia, the main goal is to progress to allogeneic bone marrow transplantation after salvage therapy. Although complete remission can be achieved with bone marrow transplantation, 4-year survival does not exceed 25-30%. Therefore, a powerful and effective salvage treatment regimen is still needed in patients with relapsed or refractory acute leukemia.
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Keywords
Klofarabin, Relaps veya refrakter akut lösemi, Yan etkiler, Clofarabine, Relaps or refractory leukemia, Advers events
Citation
Yalçın, C. vd. (2021). ''Klofarabin bazlı tedavi alan relaps veya refrakter akut lösemi tanılı hastaların retrospektif değerlendirilmesi''. Uludağ Üniversitesi Tıp Fakültesi Dergisi, 47(2), 189-193.