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Prospective, multicenter study to compare the curative effects of chemotherapy and haploidentical HSCT in first remission (CR1) for adult acute leukemia

Prospective, multicenter study to compare the curative effects of chemotherapy and haploidentical HSCT in first remission (CR1) for adult acute leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCH-10000940
Enrollment
Unknown
Registered
2010-07-02
Start date
2010-03-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult acute leukemia

Interventions

Group B:Haploidentical HSCT

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. AML and ALL diagnosed according to WHO criteria; 2. Age: 15-60 years old; 3. CR1 phase; 4. No HLA-matched sibling donor or URD; 5. Intermediate and poor risk patients with AML AND adult ALL (except for patients with t(15;17), t(8;21), inv(16)/t(16;16)); 6. Physical score 0~2 (WHO); 7. Sign the informed consent document.

Exclusion criteria

Exclusion criteria: 1. Secondary acute leukemia; 2. Contradiction of HSCT, e.g. uncontrolled active infection and severe cardiac, hepatic, renal and pulmonary disease; 3. Low- risk patients with AML (patients with t(15;17), t(8;21), inv(16)/t(16;16)); 4. Pregnant; 5. Mental disorder; 6. Complicated with outher carcinoma; 7. Cann't sign the informed consent document.

Design outcomes

Primary

MeasureTime frame
Overall survival;Disease-free survival;Relapse rate;

Secondary

MeasureTime frame
Infection rates;Immune reconstruction;

Countries

China

Contacts

Public ContactHuang Xiaojun
xjhrm@medmail.com.cn+86 13701389625

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 4, 2026