Vasudevan Nampoothiri Ram, Yeung Jonathan, Pierre Andrew, Wong Rebecca, Darling Gail, Kim John, Siu Lillian L, Chen Eric, Bouttell Elaine, Knox Jennifer, Kim Dennis Dong Huan, Lipton Jeffrey H
Hans Messner Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
Department of Thoracic Surgery, University Health Network, University of Toronto, Toronto, Ontario, Canada.
J Gastrointest Oncol. 2022 Dec;13(6):2705-2712. doi: 10.21037/jgo-22-700.
The improving survival in patients after allogeneic hematopoietic stem cell transplantation (aHCT) has warranted an increased attention to the long-term complications after aHCT especially second malignancies. The risk of developing esophageal cancer is thought to be higher than other malignancies after aHCT. There are limited data on the clinical characteristics, staging, treatment options and outcomes in these patients.
We retrospectively reviewed all patients who underwent aHCT at our centre over 30 years and identified patients who developed secondary esophageal cancer. Patients were analyzed for transplant details, disease characteristics and therapy, relapse free survival (RFS), and overall survival (OS).
Ten patients [females 40% (n=4); median age 62 years] were diagnosed with esophageal cancer after a median duration of 5.8 years since aHCT. The standardized incidence ratio (SIR) for esophageal ca after aHCT was 1.96. Five patients (55.5%) had advanced clinical stages (stage III-IV) at diagnosis. Esophagectomy (with or without neoadjuvant chemotherapy) was performed in 50% (n=5) patients. Remission was achieved in 70% (n=7) of patients while 1 patient had progressive disease after planned treatment. Progressive disease was the cause in 50% (n=3) of deaths. Estimated 2- and 5-year overall survival after diagnosis of esophageal cancer was 60% and 45% respectively (median survival: 44.1 months).
Despite the higher risk and increased incidence of esophageal cancer after aHCT, the outcomes these patients may be comparable to that in general population if diagnosed early. This implies the need for continued long term follow-up for patients after aHCT with a transplant physician.
异基因造血干细胞移植(aHCT)后患者生存率的提高使得人们越来越关注aHCT后的长期并发症,尤其是第二原发性恶性肿瘤。aHCT后发生食管癌的风险被认为高于其他恶性肿瘤。关于这些患者的临床特征、分期、治疗选择和预后的数据有限。
我们回顾性分析了30年来在本中心接受aHCT的所有患者,并确定了发生继发性食管癌的患者。分析患者的移植细节、疾病特征和治疗情况、无复发生存期(RFS)和总生存期(OS)。
10例患者[女性占40%(n = 4);中位年龄62岁]在aHCT后中位5.8年被诊断为食管癌。aHCT后食管癌的标准化发病比(SIR)为1.96。5例患者(55.5%)在诊断时处于临床晚期(III-IV期)。50%(n = 5)的患者接受了食管切除术(有或无新辅助化疗)。70%(n = 7)的患者病情缓解,而1例患者在计划治疗后病情进展。病情进展是50%(n = 3)患者死亡的原因。食管癌诊断后的估计2年和5年总生存率分别为60%和45%(中位生存期:44.1个月)。
尽管aHCT后食管癌风险较高且发病率增加,但如果早期诊断,这些患者的预后可能与一般人群相当。这意味着aHCT后的患者需要移植医生进行持续的长期随访。