Fixed-dose inotuzumab ozogamicin (INO) combined with Vincristine and Prednisone (VP) regimen as induction therapy for newly diagnosed B-cell acute lymphocytic leukemia (B-ALL): a multi-center, open-label, single-arm, prospective clinical study

Adult B-ALL exhibits significant heterogeneity and poor prognosis compared with the pediatric population. While the complete remission (CR) rate of traditional induction chemotherapy is 70%–90% for newly diagnosed patients [ 1 ], only 30–50% of patients attain long-term disease-free survival (DFS) exceeding 5-years [ 2 ]. For the Philadelphia chromosome-positive (ph+) patients, the addition of tyrosine kinase inhibitors (TKIs) significantly improved the CR rates [ 3 ]. In addition, achieving measurable residual disease (MRD) negativity (<10 −4 leukemic blasts), particularly early MRD negativity, is a critical determinant for long-term survival and reduces relapse [ 4 ]. Despite improvements in CR rates with traditional therapy, approximately half of them are still detected MRD positive [ 4 ]. Persistent MRD positivity is considered an independent adverse prognosis factor [ 5 ], whereas early achievement of MRD negativity in CR was associated with sustained remission [ 6 ].

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Publication Details

Journal
Blood Cancer Journal
Published
2026-07-28
DOI
https://doi.org/10.1038/s41408-026-01589-6
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
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article

Fixed-dose inotuzumab ozogamicin (INO) combined with Vincristine and Prednisone (VP) regimen as induction therapy for newly diagnosed B-cell acute lymphocytic leukemia (B-ALL): a multi-center, open-label, single-arm, prospective clinical study

Qiang Song, Guanchen Bai, Erlie Jiang, Xuemei Qin et al.
Blood Cancer Journal
Acute Lymphoblastic Leukemia research
article

Fixed-dose inotuzumab ozogamicin (INO) combined with Vincristine and Prednisone (VP) regimen as induction therapy for newly diagnosed B-cell acute lymphocytic leukemia (B-ALL): a multi-center, open-label, single-arm, prospective clinical study

Qiang Song, Guanchen Bai, Erlie Jiang, Xuemei Qin, Kaifeng Wang, Jilei Zhang, Dexiao Kong, Yuyu Liu, Lin Dong, Jie Zou, Sifeng Gao, Chenglu Yuan, Qiang Li, Lei Ju, Jun Peng, Donglin Yang, Yan Guo, Qingliang Teng, Yan Shi
article en

Abstract

Adult B-ALL exhibits significant heterogeneity and poor prognosis compared with the pediatric population. While the complete remission (CR) rate of traditional induction chemotherapy is 70%–90% for newly diagnosed patients [ 1 ], only 30–50% of patients attain long-term disease-free survival (DFS) exceeding 5-years [ 2 ]. For the Philadelphia chromosome-positive (ph+) patients, the addition of tyrosine kinase inhibitors (TKIs) significantly improved the CR rates [ 3 ]. In addition, achieving measurable residual disease (MRD) negativity (<10 −4 leukemic blasts), particularly early MRD negativity, is a critical determinant for long-term survival and reduces relapse [ 4 ]. Despite improvements in CR rates with traditional therapy, approximately half of them are still detected MRD positive [ 4 ]. Persistent MRD positivity is considered an independent adverse prognosis factor [ 5 ], whereas early achievement of MRD negativity in CR was associated with sustained remission [ 6 ].

Blood Cancer JournalVol. 16(1)
Qingdao University (CN), Shandong University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Zhangqiu City People's Hospital (CN), Second Hospital of Shandong University (CN), Shandong Provincial Hospital (CN), Institute of Hematology & Blood Diseases Hospital (CN), Taian City Central Hospital (CN), Liaocheng People's Hospital (CN), Qilu Hospital of Shandong University (CN), First Affiliated Hospital of Jinan University (CN), Shandong First Medical University (CN)
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Openalex Percentile: Top 7%
Acute Lymphoblastic Leukemia research
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