Yuan Lei, Sun Lu, Bo Jian, Zhou Ying, Li Hong-hua, Yu Li, Gao Chun-ji
Division of Hematology and Bone Marrow Transplantation, Chinese PLA General Hospital, Beijing, PR China.
Ann Transplant. 2011 Jul-Sep;16(3):135-8. doi: 10.12659/aot.882007.
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an uncommon subtype of peripheral T-cell lymphoma and its standard treatment remains ongoing study. Cases refractory to chemotherapy are suggested to benefit from autologous hematopoietic stem cell transplantation (auto-HSCT). Nevertheless, post auto-HSCT recurrence seems to be irreversible. Very few cases of allogeneic-HSCT (allo-HSCT) in SPTCL have been reported so far.
A 27-year-old female presented to our hospital with refractory SPTCL for receiving auto-HSCT. Cutaneous biopsy had confirmed diagnosis of SPTCL at a local hospital, where 5 lines and 10 cycles of intensive chemotherapy had been prescribed. All these treatment provided marginal control of disease progression. After her enrollment at our institute, she relapsed again after the collection of peripheral hematopoietic stem cells. Then, we performed an allo-HSCT to her from a 10/10 matched unrelated donor. Neutrophil and platelet engraftment occurred at day +11 and +13, respectively. At day +15, lymphoma, however, came back, resulting in the withdrawal of cyclosporine from day +35 to day +75, when acute graft versus host disease (aGvHD) emerged. Lymphoma cells were observed in a subcutaneous biopsy from her leg. Eventually, skin manifestation of extensive chronic GvHD developed. By present, the patient has sustained complete remission for 18 months.
Allo-HSCT is rational for patients with refractory SPTCL. To our knowledge, this is the first case, with regained remission after post allo-HSCT relapse through cyclosporine withdrawal, showing the existence of graft versus lymphoma (GvL) effect in SPTCL.
皮下脂膜炎样T细胞淋巴瘤(SPTCL)是外周T细胞淋巴瘤的一种罕见亚型,其标准治疗仍在研究中。对化疗难治的病例建议从自体造血干细胞移植(auto-HSCT)中获益。然而,自体造血干细胞移植后复发似乎是不可逆的。迄今为止,SPTCL中异基因造血干细胞移植(allo-HSCT)的病例报道非常少。
一名27岁女性因难治性SPTCL到我院接受自体造血干细胞移植。皮肤活检在当地医院确诊为SPTCL,在那里已进行了5线10周期的强化化疗。所有这些治疗仅对疾病进展有一定控制。她入我院后,在外周造血干细胞采集后再次复发。然后,我们从一名10/10配型的无关供者为她进行了异基因造血干细胞移植。中性粒细胞和血小板分别在+11天和+13天植入。然而,在+15天淋巴瘤复发,导致从+35天至+75天停用环孢素,此时出现了急性移植物抗宿主病(aGvHD)。在她腿部的皮下活检中观察到淋巴瘤细胞。最终,出现了广泛慢性移植物抗宿主病的皮肤表现。目前,该患者已持续完全缓解18个月。
异基因造血干细胞移植对难治性SPTCL患者是合理的。据我们所知,这是第一例异基因造血干细胞移植后复发通过停用环孢素而再次缓解的病例,表明SPTCL中存在移植物抗淋巴瘤(GvL)效应。