Acute Lymphoblastic Leukemia Clinical Trial
Official title:
A Prospective Study of Intensified Conditioning Regimen With High-Dose-Etoposide for Allogeneic Hematopoietic Stem Cell Transplantation for Adult Acute Lymphoblastic Leukemia in China
Evolving paradigms in the treatment of adult ALL include the application of intense pediatric
regimens to the treatment of adolescents and young adults (AYA) and the optimization of
allogeneic hematopoietic stem cell transplantation (allo-HSCT) in the cure of patients. The
Cancer and Leukemia Group B (CALGB) and the Children's Cancer Group (CCG) first asked whether
AYA between the ages of 16 and 20 fared differently whether they were treated on pediatric
protocols. The results of this study demonstrated that although the complete remission rates
were identical for the AYAs treated on the CALGB and CCG trials, the AYAs had a 63%
event-free survival (EFS) and 67% OS at 7 years on the CCG trials compared with 34% and 46%,
respectively, on the CALGB trials.
High relapse and transplantation-related-mortality still remains great challenge for HSCT of
adult ALL, which both range between 25% and 30%. Recently, risk-adapted indication and
optimization of conditioning regimen are highlighted, which aiming to reduce TRM and relapse
rate, respectively.City of Hope National Medical Center studied the substitution of etoposide
(VP-16) for CY in the treatment of ALL patients receiving HCT. The result suggested that
etoposide and TBI are associated with a decreased relapse rate following transplantation for
ALL, compared with those receiving CY and TBI. Japanese and Germany reports pronounced the
advantage of VP-16 in intensified regimen for adult ALL. On the same time, the investigators
previous researches have confirmed the effect and safety of FA-intensified conditioning
regimen on relapse and refractary leukemia.
Based on mentioned above, the investigators speculate that VP-16-intensified conditioning
regimen could improve the outcome for adult ALL. The potential mechanism will be attributed
to reduce MRD and promote GVL effect via providing enough time-window for
immuno-reconstitution by high-dose preparative regimen.
In the first decade of the new millennium, multiple studies have begun to change our thinking
about the treatment of adults with acute lymphoblastic leukemia (ALL). In pediatric patients
cure rates in the range of 80% to 90% are now attainable. While adult patients with ALL now
have a 90% complete remission (CR) with modern chemotherapy, most patients will relapse, and
leukemia-free survival with 3 to 7 years of follow-up in large series is only in the range of
30% to 40%. The poor outcome of chemotherapy in adults with ALL as compared to children
relates to multiple factors, including poor tolerance of intensive courses of chemotherapy
and a higher incidence of poor prognostic subtypes of ALL such as Philadelphia
chromosome-positive ALL and a lower incidence of favorable subtypes such as the t (12; 21).
Evolving paradigms in the treatment of adult ALL include the application of intense pediatric
regimens to the treatment of adolescents and young adults (AYA) and the optimization of
allogeneic hematopoietic stem cell transplantation (allo-HSCT) in the cure of patients. Adult
regimens are typically less intense than pediatric regimens. The Cancer and Leukemia Group B
(CALGB) and the Children's Cancer Group (CCG) first asked whether AYA between the ages of 16
and 20 fared differently whether they were treated on pediatric protocols. The results of
this study demonstrated that although the complete remission rates were identical for the
AYAs treated on the CALGB and CCG trials, the AYAs had a 63% event-free survival (EFS) and
67% OS at 7 years on the CCG trials compared with 34% and 46%, respectively, on the CALGB
trials. These results have prompted new studies where pediatric ALL regimens have been
adapted to the treatment of younger adults. With short follow-up, GRAALL-2003 reports suggest
EFS and OS outcomes in the range of 60%. This improved outcome was more pronounced in the
standard-risk patients with a donor who had an OS at 5 years of 69%. On the same time, our
previous researches have confirmed the effect and safety of FA-intensified conditioning
regimen on relapse and refractary leukemia.
Based on mentioned above, we speculate that VP-16-intensified conditioning regimen could
improve the outcome for adult ALL. The potential mechanism will be attributed to reduce MRD
and promote GVL effect via providing enough time-window for immuno-reconstitution by
high-dose preparative regimen.
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