Phase 2
N=17
LSA4 Protocol for the Treatment of Advanced Pediatric and Adolescent Non-Hodgkins Lymphoma
Non-Hodgkin's Lymphoma
Bottom Line
View on ClinicalTrials.gov: NCT00610883 ↗Enrolled (actual)
17
Serious AEs
5.9%
Results posted
Jan 2016
Primary outcome: Primary: Complete Remission — 10 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- LSA4, Cyclophosphamide, Methotrexate, Daunomycin, L-asparaginase, BCNU (Drug)
- Age
- Pediatric, Adult
- Sex
- All
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Primary completion
- Dec 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Complete Remission |
10 | — |
Summary
Non-Hodgin's lymphoma is curable in 76% of patients. In nonlymphoblastic lymphmas, cancer may return on average 3 months from beginning treatment and for lymphoblastic lymphomas, 6 months. To aggressively treat this cancer this study uses effective drugs in three parts:
* Induction ends on day 19
* Consolidation ends on day 38 or 42
* Maintenance may include up to 6 cycles
Eligibility Criteria
Inclusion Criteria
- Non-Hodgkin's Lymphoma stages III, IV, IVA with
- T cell lymphomas, any primary site irrespective of LDH level
- large cell lymphomas, any primary site irrespective of LDH level
- B cell lymphomas, any primary site with initial LDH of less than 500
Exclusion Criteria
- B cell lymphomas, any primary site with initial LDH of less than 500 and initial CNS or bone involvement
Data sourced from ClinicalTrials.gov (NCT00610883). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.