Dong Won Baek, Sang Kyun Sohn, Sung-Hoon Jung, Ga-Young Song, Ik-Chan Song, Jeong Suk Koh, Ho-Jin Shin, Do Young Kim, Sung-Hyun Kim, Ji Hyun Lee, Sung-Nam Lim, Won Sik Lee, Young Rok Do, Min Kyoung Kim, Young Hoon Park, Hyeon-Seok Eom, Ki Sun Jung, Jee Hyun Kong, Joon Ho Moon
{"title":"早期使用blinatumumab治疗复发/难治性b细胞急性淋巴细胞白血病成年患者的生存获益","authors":"Dong Won Baek, Sang Kyun Sohn, Sung-Hoon Jung, Ga-Young Song, Ik-Chan Song, Jeong Suk Koh, Ho-Jin Shin, Do Young Kim, Sung-Hyun Kim, Ji Hyun Lee, Sung-Nam Lim, Won Sik Lee, Young Rok Do, Min Kyoung Kim, Young Hoon Park, Hyeon-Seok Eom, Ki Sun Jung, Jee Hyun Kong, Joon Ho Moon","doi":"10.1016/j.clml.2025.09.004","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>This study analyzed the long-term survival of blinatumomab-treated patients in the salvage setting and factors affecting treatment outcomes.</p><p><strong>Methods: </strong>Clinical data were collected from adult patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (ALL) who were administered blinatumomab as a salvage therapy.</p><p><strong>Results: </strong>A total of 138 patients with R/R B-cell ALL were analyzed, of which 99 patients were diagnosed with Philadelphia chromosome-negative (Ph-negative) ALL, and 39 patients were treated for Ph-positive ALL. After 2 cycles of blinatumomab therapy, 45 patients (45.5%) achieved complete remission (CR), and 10 (10.1%) showed complete remission with partial hematological response (CRh), while 32 (32.3%) showed no response in the Ph-negative ALL subgroup. In the Ph-positive ALL subgroup, 18 patients (46.2%) achieved CR, and 4 (10.3%) achieved CRh, while 13 (33.3%) were refractory. In the Ph-negative ALL subgroup, for both relapse-free survival (RFS) and overall survival (OS), PLT < 100.0 (× 10<sup>3</sup>/µL) and number of prior treatment lines ≥ 2 were adverse prognostic factors, while proceeding to allo-SCT was a favorable factor. In the Ph-positive ALL subgroup, number of prior treatment lines ≥ 3 and refractory status at blinatumomab initiation were adverse factors for RFS. PLT < 100.0 (× 10<sup>3</sup>/µL) and refractory status were adverse factors, while proceeding to allo-SCT was a favorable factor for OS.</p><p><strong>Conclusion: </strong>Early use of blinatumomab showed survival benefits in both Ph-negative and Ph-positive ALL subgroups in the salvage setting. Proceeding to allo-SCT after blinatumomab could improve long-term outcomes in patients with Ph-negative ALL.</p>","PeriodicalId":10348,"journal":{"name":"Clinical Lymphoma, Myeloma & Leukemia","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Survival Benefits of Early Treatment With Blinatumomab in Adult Patients With Relapsed/Refractory B-Cell Acute Lymphoblastic Leukemia.\",\"authors\":\"Dong Won Baek, Sang Kyun Sohn, Sung-Hoon Jung, Ga-Young Song, Ik-Chan Song, Jeong Suk Koh, Ho-Jin Shin, Do Young Kim, Sung-Hyun Kim, Ji Hyun Lee, Sung-Nam Lim, Won Sik Lee, Young Rok Do, Min Kyoung Kim, Young Hoon Park, Hyeon-Seok Eom, Ki Sun Jung, Jee Hyun Kong, Joon Ho Moon\",\"doi\":\"10.1016/j.clml.2025.09.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>This study analyzed the long-term survival of blinatumomab-treated patients in the salvage setting and factors affecting treatment outcomes.</p><p><strong>Methods: </strong>Clinical data were collected from adult patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (ALL) who were administered blinatumomab as a salvage therapy.</p><p><strong>Results: </strong>A total of 138 patients with R/R B-cell ALL were analyzed, of which 99 patients were diagnosed with Philadelphia chromosome-negative (Ph-negative) ALL, and 39 patients were treated for Ph-positive ALL. After 2 cycles of blinatumomab therapy, 45 patients (45.5%) achieved complete remission (CR), and 10 (10.1%) showed complete remission with partial hematological response (CRh), while 32 (32.3%) showed no response in the Ph-negative ALL subgroup. In the Ph-positive ALL subgroup, 18 patients (46.2%) achieved CR, and 4 (10.3%) achieved CRh, while 13 (33.3%) were refractory. In the Ph-negative ALL subgroup, for both relapse-free survival (RFS) and overall survival (OS), PLT < 100.0 (× 10<sup>3</sup>/µL) and number of prior treatment lines ≥ 2 were adverse prognostic factors, while proceeding to allo-SCT was a favorable factor. In the Ph-positive ALL subgroup, number of prior treatment lines ≥ 3 and refractory status at blinatumomab initiation were adverse factors for RFS. PLT < 100.0 (× 10<sup>3</sup>/µL) and refractory status were adverse factors, while proceeding to allo-SCT was a favorable factor for OS.</p><p><strong>Conclusion: </strong>Early use of blinatumomab showed survival benefits in both Ph-negative and Ph-positive ALL subgroups in the salvage setting. Proceeding to allo-SCT after blinatumomab could improve long-term outcomes in patients with Ph-negative ALL.</p>\",\"PeriodicalId\":10348,\"journal\":{\"name\":\"Clinical Lymphoma, Myeloma & Leukemia\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Lymphoma, Myeloma & Leukemia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.clml.2025.09.004\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Lymphoma, Myeloma & Leukemia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.clml.2025.09.004","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Survival Benefits of Early Treatment With Blinatumomab in Adult Patients With Relapsed/Refractory B-Cell Acute Lymphoblastic Leukemia.
Background: This study analyzed the long-term survival of blinatumomab-treated patients in the salvage setting and factors affecting treatment outcomes.
Methods: Clinical data were collected from adult patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (ALL) who were administered blinatumomab as a salvage therapy.
Results: A total of 138 patients with R/R B-cell ALL were analyzed, of which 99 patients were diagnosed with Philadelphia chromosome-negative (Ph-negative) ALL, and 39 patients were treated for Ph-positive ALL. After 2 cycles of blinatumomab therapy, 45 patients (45.5%) achieved complete remission (CR), and 10 (10.1%) showed complete remission with partial hematological response (CRh), while 32 (32.3%) showed no response in the Ph-negative ALL subgroup. In the Ph-positive ALL subgroup, 18 patients (46.2%) achieved CR, and 4 (10.3%) achieved CRh, while 13 (33.3%) were refractory. In the Ph-negative ALL subgroup, for both relapse-free survival (RFS) and overall survival (OS), PLT < 100.0 (× 103/µL) and number of prior treatment lines ≥ 2 were adverse prognostic factors, while proceeding to allo-SCT was a favorable factor. In the Ph-positive ALL subgroup, number of prior treatment lines ≥ 3 and refractory status at blinatumomab initiation were adverse factors for RFS. PLT < 100.0 (× 103/µL) and refractory status were adverse factors, while proceeding to allo-SCT was a favorable factor for OS.
Conclusion: Early use of blinatumomab showed survival benefits in both Ph-negative and Ph-positive ALL subgroups in the salvage setting. Proceeding to allo-SCT after blinatumomab could improve long-term outcomes in patients with Ph-negative ALL.
期刊介绍:
Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.