Xiaoye Yuan, Qixin Guo, Zewen Zhang
This case suggests that refractory CTIT characterized by predominant megakaryocytic involvement may occur during ATO maintenance therapy, with clinical features potentially differing from those of conventional cytotoxic chemotherapy-related CTIT. Romiplostim may promote the recovery of residual megakaryopoietic capacity and provide a potential therapeutic option for such patients. However, its precise mechanism of action and the patient populations most likely to benefit require further investigation.
BACKGROUND: All-trans retinoic acid (ATRA) combined with arsenic trioxide (ATO) is a first-line treatment regimen for acute promyelocytic leukemia (APL), with generally milder myelosuppressive effects compared with conventional chemotherapy. Although standard-dose ATO is not typically considered a major risk factor for cancer treatment-induced thrombocytopenia (CTIT), severe and persistent thrombocytopenia may still occur during ATO maintenance therapy, and its clinical characteristics and therapeutic strategies remain unclear.
CASE PRESENTATION: A 60-year-old female patient with APL developed refractory grade 3-4 thrombocytopenia during ATO maintenance therapy, with no significant response to recombinant human thrombopoietin or hetrombopag treatment (platelet nadir: 8 × 109/L; duration of platelet count <50 × 109/L: 8 weeks). Subsequently, romiplostim (250 μg/week) was administered, resulting in platelet recovery to 151 × 109/L within 3 weeks, accompanied by restoration of megakaryocyte numbers and reappearance of platelet-producing megakaryocytes in the bone marrow. The patient subsequently resumed maintenance therapy and completed the remaining treatment cycles with romiplostim support, maintaining continuous molecular remission during follow-up.
CONCLUSION: This case suggests that refractory CTIT characterized by predominant megakaryocytic involvement may occur during ATO maintenance therapy, with clinical features potentially differing from those of conventional cytotoxic chemotherapy-related CTIT. Romiplostim may promote the recovery of residual megakaryopoietic capacity and provide a potential therapeutic option for such patients. However, its precise mechanism of action and the patient populations most likely to benefit require further investigation.