Venkateswaran V Swaminathan, Ramya Uppuluri, Satish K Meena, Harika Varla, Rumesh Chandar, Revathi Raj
{"title":"单倍体干细胞移植治疗新诊断的高危神经母细胞瘤:来自印度的单臂前瞻性研究结果","authors":"Venkateswaran V Swaminathan, Ramya Uppuluri, Satish K Meena, Harika Varla, Rumesh Chandar, Revathi Raj","doi":"10.4103/ijc.ijc_999_21","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>With increasing data on graft-versus-tumor (GVT) effect in neuroblastoma, we aimed to evaluate the possibility of haploidentical stem cell transplantation (HSCT) as a technique to induce GVT and thereby improve outcomes in high-risk neuroblastoma.</p><p><strong>Patients and methods: </strong>We performed a prospective, single-arm study and included children from 18 months to 18 years of age diagnosed with high-risk neuroblastoma and who underwent a haploidentical HSCT from a parent donor. All children were started on induction chemotherapy as per the SIOP-Europa-Neuroblastoma (SIOPEN) protocol, followed by assessment and surgery when feasible. Conditioning in the unmanipulated graft included thiotepa/fludarabine/busulfan. With a T-depleted graft, conditioning included rabbit anti-thymocyte globulin/fludarabine/thiotepa/melphalan.</p><p><strong>Results: </strong>Of the five children, one child received T-depleted and four children received T-replete stem cells with posttransplant cyclophosphamide, with 100% engraftment, no regimen-related toxicities, and documented remission. Grade I/II skin GVHD occurred in all children who responded to steroids. We administered involved-field radiotherapy in four children around D + 60-75 post-HSCT, followed by 13-cis retinoic acid. At 1 year post-HSCT, three had isolated central nervous system relapse; one child had isolated pelvic bone relapse. One child relapsed 2 months post-HSCT. Progression-free survival was 12 months in 4/5 children and 6 months in one child. All except one child succumbed to progressive disease post relapse.</p><p><strong>Conclusion: </strong>Children with high-risk neuroblastoma continued to relapse within a year post-HSCT in our cohort. Significant improvement in outcomes was not demonstrated with haploidentical HSCT. We urgently need new strategies including deeper remission induction with upfront metaiodobenzylguanidine (MIBG) therapy followed by HSCT to improve the outcomes.</p>","PeriodicalId":13505,"journal":{"name":"Indian journal of cancer","volume":"62 1","pages":"32-36"},"PeriodicalIF":0.9000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Haploidentical stem cell transplantation in newly diagnosed high-risk neuroblastoma: Results from a single-arm, prospective study from India.\",\"authors\":\"Venkateswaran V Swaminathan, Ramya Uppuluri, Satish K Meena, Harika Varla, Rumesh Chandar, Revathi Raj\",\"doi\":\"10.4103/ijc.ijc_999_21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>With increasing data on graft-versus-tumor (GVT) effect in neuroblastoma, we aimed to evaluate the possibility of haploidentical stem cell transplantation (HSCT) as a technique to induce GVT and thereby improve outcomes in high-risk neuroblastoma.</p><p><strong>Patients and methods: </strong>We performed a prospective, single-arm study and included children from 18 months to 18 years of age diagnosed with high-risk neuroblastoma and who underwent a haploidentical HSCT from a parent donor. All children were started on induction chemotherapy as per the SIOP-Europa-Neuroblastoma (SIOPEN) protocol, followed by assessment and surgery when feasible. Conditioning in the unmanipulated graft included thiotepa/fludarabine/busulfan. With a T-depleted graft, conditioning included rabbit anti-thymocyte globulin/fludarabine/thiotepa/melphalan.</p><p><strong>Results: </strong>Of the five children, one child received T-depleted and four children received T-replete stem cells with posttransplant cyclophosphamide, with 100% engraftment, no regimen-related toxicities, and documented remission. Grade I/II skin GVHD occurred in all children who responded to steroids. We administered involved-field radiotherapy in four children around D + 60-75 post-HSCT, followed by 13-cis retinoic acid. At 1 year post-HSCT, three had isolated central nervous system relapse; one child had isolated pelvic bone relapse. One child relapsed 2 months post-HSCT. Progression-free survival was 12 months in 4/5 children and 6 months in one child. All except one child succumbed to progressive disease post relapse.</p><p><strong>Conclusion: </strong>Children with high-risk neuroblastoma continued to relapse within a year post-HSCT in our cohort. Significant improvement in outcomes was not demonstrated with haploidentical HSCT. We urgently need new strategies including deeper remission induction with upfront metaiodobenzylguanidine (MIBG) therapy followed by HSCT to improve the outcomes.</p>\",\"PeriodicalId\":13505,\"journal\":{\"name\":\"Indian journal of cancer\",\"volume\":\"62 1\",\"pages\":\"32-36\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian journal of cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.4103/ijc.ijc_999_21\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/16 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian journal of cancer","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4103/ijc.ijc_999_21","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/16 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
Haploidentical stem cell transplantation in newly diagnosed high-risk neuroblastoma: Results from a single-arm, prospective study from India.
Background: With increasing data on graft-versus-tumor (GVT) effect in neuroblastoma, we aimed to evaluate the possibility of haploidentical stem cell transplantation (HSCT) as a technique to induce GVT and thereby improve outcomes in high-risk neuroblastoma.
Patients and methods: We performed a prospective, single-arm study and included children from 18 months to 18 years of age diagnosed with high-risk neuroblastoma and who underwent a haploidentical HSCT from a parent donor. All children were started on induction chemotherapy as per the SIOP-Europa-Neuroblastoma (SIOPEN) protocol, followed by assessment and surgery when feasible. Conditioning in the unmanipulated graft included thiotepa/fludarabine/busulfan. With a T-depleted graft, conditioning included rabbit anti-thymocyte globulin/fludarabine/thiotepa/melphalan.
Results: Of the five children, one child received T-depleted and four children received T-replete stem cells with posttransplant cyclophosphamide, with 100% engraftment, no regimen-related toxicities, and documented remission. Grade I/II skin GVHD occurred in all children who responded to steroids. We administered involved-field radiotherapy in four children around D + 60-75 post-HSCT, followed by 13-cis retinoic acid. At 1 year post-HSCT, three had isolated central nervous system relapse; one child had isolated pelvic bone relapse. One child relapsed 2 months post-HSCT. Progression-free survival was 12 months in 4/5 children and 6 months in one child. All except one child succumbed to progressive disease post relapse.
Conclusion: Children with high-risk neuroblastoma continued to relapse within a year post-HSCT in our cohort. Significant improvement in outcomes was not demonstrated with haploidentical HSCT. We urgently need new strategies including deeper remission induction with upfront metaiodobenzylguanidine (MIBG) therapy followed by HSCT to improve the outcomes.
期刊介绍:
Indian Journal of Cancer (ISSN 0019-509X), the show window of the progress of ontological sciences in India, was established in 1963. Indian Journal of Cancer is the first and only periodical serving the needs of all the specialties of oncology in India.