Long-Term Rather than Short-Term Survival Benefit in Mantle Cell Lymphoma Patients Treated With Intensive Chemo- Immunotherapy and Hematopoietic Stem Cell Transplantation in Real World Experience
{"title":"Long-Term Rather than Short-Term Survival Benefit in Mantle Cell Lymphoma Patients Treated With Intensive Chemo- Immunotherapy and Hematopoietic Stem Cell Transplantation in Real World Experience","authors":"Tan Td","doi":"10.23880/hij-16000172","DOIUrl":null,"url":null,"abstract":"Purpose: Mantle cell lymphoma is an aggressive B cell lymphoma with initially responded but easy to relapse and difficult to cure without survival plateau. The present recommendation of treatment includes induction chemo-immunotherapy followed by high dose chemotherapy plus autologous hematopoietic stem cell transplantation for transplant-eligible patients and chemo- immunotherapy followed by rituximab maintenance for transplant-ineligible patients. However, the best induction regimen remains to be defined and median five-year overall survival is around 60% on phase II trials of multi-center experiences. Materials & Methods: We investigated the real world outcome of our patients undergoing different regimens of induction chemo-immunotherapy and analyzed whether the intensity of treatment as one of prognostic factors upon the impact of survival. Results: Between 1997 and 2018, we analyzed 50 patients as the cohort with median age 62 (range 34 to 77), and male to female was 40 versus 10. Advanced stage of diseases were 86% (stage III 10% and stage IV 76%) of all patients. Ki-67 more than 30% of lymphomas were seen in 50% of patients and 34% with Ki-67 less than 30% and 16% were unknown. Thirty-four per cents of patients underwent intensive induction chemo-immunotherapy with or without ASCT and 66% received non- intensive treatment. Six of 31 relapsed patients had undergone allogeneic hematopoietic stem cell transplantation. Five-year overall survival was 52% with median OS 5.15 years. There was no significant survival difference between intensive versus non-intensive induction therapy with 53% versus 46% in first 5 years, however, better overall survival was seen in intensive therapy group when follow up longer. High Ki-67 patients had shorter 5-year overall survival (37% vs 63%). Transplant patients had better overall survival with 68% vs 47% in 5 years with median OS 10.86 vs 4.34 years. Conclusion: There was no statistically significant difference of survival during the initial five years but intensive induction chemo-immunotherapy with or without HDC/ASCT could achieve better survival in longer follow-up according to our real world experience.","PeriodicalId":245976,"journal":{"name":"Haematology International Journal","volume":"204 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Haematology International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23880/hij-16000172","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Mantle cell lymphoma is an aggressive B cell lymphoma with initially responded but easy to relapse and difficult to cure without survival plateau. The present recommendation of treatment includes induction chemo-immunotherapy followed by high dose chemotherapy plus autologous hematopoietic stem cell transplantation for transplant-eligible patients and chemo- immunotherapy followed by rituximab maintenance for transplant-ineligible patients. However, the best induction regimen remains to be defined and median five-year overall survival is around 60% on phase II trials of multi-center experiences. Materials & Methods: We investigated the real world outcome of our patients undergoing different regimens of induction chemo-immunotherapy and analyzed whether the intensity of treatment as one of prognostic factors upon the impact of survival. Results: Between 1997 and 2018, we analyzed 50 patients as the cohort with median age 62 (range 34 to 77), and male to female was 40 versus 10. Advanced stage of diseases were 86% (stage III 10% and stage IV 76%) of all patients. Ki-67 more than 30% of lymphomas were seen in 50% of patients and 34% with Ki-67 less than 30% and 16% were unknown. Thirty-four per cents of patients underwent intensive induction chemo-immunotherapy with or without ASCT and 66% received non- intensive treatment. Six of 31 relapsed patients had undergone allogeneic hematopoietic stem cell transplantation. Five-year overall survival was 52% with median OS 5.15 years. There was no significant survival difference between intensive versus non-intensive induction therapy with 53% versus 46% in first 5 years, however, better overall survival was seen in intensive therapy group when follow up longer. High Ki-67 patients had shorter 5-year overall survival (37% vs 63%). Transplant patients had better overall survival with 68% vs 47% in 5 years with median OS 10.86 vs 4.34 years. Conclusion: There was no statistically significant difference of survival during the initial five years but intensive induction chemo-immunotherapy with or without HDC/ASCT could achieve better survival in longer follow-up according to our real world experience.
目的:套细胞淋巴瘤是一种侵袭性B细胞淋巴瘤,初期有应答,但易复发,无生存平台,难以治愈。目前推荐的治疗方法包括:适合移植的患者,诱导化疗-免疫治疗后再进行大剂量化疗+自体造血干细胞移植;不适合移植的患者,化疗-免疫治疗后再进行美罗华维持。然而,最佳诱导方案仍有待确定,在多中心经验的II期试验中,中位5年总生存率约为60%。材料与方法:我们调查了接受不同诱导化疗-免疫治疗方案的患者的真实世界结果,并分析了治疗强度是否作为影响生存的预后因素之一。结果:在1997年至2018年期间,我们分析了50例患者作为队列,中位年龄为62岁(范围为34至77岁),男女比例为40比10。晚期疾病占所有患者的86% (III期10%,IV期76%)。50%的患者中有超过30%的淋巴瘤Ki-67, 34%的患者Ki-67低于30%,16%的患者未知。34%的患者接受了有或没有ASCT的强化诱导化学免疫治疗,66%的患者接受了非强化治疗。31例复发患者中有6例接受了异基因造血干细胞移植。5年总生存率为52%,中位OS为5.15年。强化与非强化诱导治疗前5年的生存率无显著差异,分别为53%和46%,但随着随访时间的延长,强化治疗组的总生存率更高。高Ki-67患者的5年总生存率较短(37% vs 63%)。移植患者的5年总生存率为68% vs 47%,中位OS为10.86 vs 4.34年。结论:前5年生存率无统计学差异,但根据我们的实际经验,强化诱导化疗免疫治疗联合或不联合HDC/ASCT可在较长随访时间内获得更好的生存率。