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WithdrawnNCT00488605Updated Aug 3, 2023

H-9926-LCH III: Treatment Protocol of the Third International Study for Langerhans Cell Histiocytosis

A Phase 3 interventional study of Prednisone, Vinblastin, 6-mercaptopuroine and Leucovorin, Methotrexate, Vinblastine, Prednisone in Leukemia, sponsored by University of New Mexico. Withdrawn at 1 site in United States. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2023-08-03.

Sponsored by University of New Mexico · Phase 3, Interventional, and Treatment

Why this study was withdrawn
This is a duplicate record and the sponsor has registered the study.
Phase
Phase 3
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
Up to 18 Years
Sex
All
01

Study summary

LCH III is an international, multicentric, prospective clinical study comprised of:

  • a randomized clinical trial for multisystem "RISK" patients and
  • a randomized clinical trial for multisystem "LOW RISK" patients and
  • a pilot study for patients with single system MFB and localized "SPECIAL SITES"
Read the detailed description

Therapy for "LOW RISK" Patients:

The decision as to which research program you will be assigned will be made entirely by chance. The overall time of therapy will be 6 or 12 months as randomly assigned. The research program will be with the drugs Vinblastine and Prednisone.

Initial Therapy

  1. Prednisone given by mouth three times a day daily as a four-week course, then gradually decreased over 2 more weeks.
  2. Vinblastine will be given IV (into a vein) one day a week for 6 weeks.
  3. Patients who have no evidence of active disease at this time will proceed to continuation therapy.

Patients whose disease response is stable, mixed or worse will receive additional therapy with:

  1. Prednisone in 3 divided doses by mouth for 3 days every week, from week 7-12.
  2. Vinblastine IV one day a week for 6 more weeks.

    • If the disease is gone or better after this additional therapy continuation will begin.

Continuation Therapy

  1. Prednisone in 3 doses daily day 1-5 every 3 weeks until the end of month 6 or 12 from start of therapy, as randomized.
  2. Vinblastine IV day 1 every 3 weeks until the end of month 6 or 12 from start of therapy, as randomized.

Therapy for "SPECIAL SITE" (Multi-focal Bone Involvement) Patients:

Treatment consists of an initial treatment of 6 weeks and a continuation treatment. A second course is given only to patients with progressive disease. The overall therapy time period is 6 months.

Initial Therapy 4. Prednisone given by mouth three times a day daily as a four-week course, then gradually decreased over 2 more weeks.

  1. Vinblastine will be given IV (into a vein) one day a week for 6 weeks. 6. Patients who have no evidence of active disease at this time will proceed to continuation therapy.

Patients whose disease response is stable, mixed or worse will receive additional therapy with:

  1. Prednisone in 3 divided doses days 1-3 weekly from week 7-12. 4. Vinblastine IV one day a week for 6 more weeks.
  • If the disease is gone or better after this additional therapy continuation will begin.

Continuation Therapy 3. Prednisone in 3 doses daily day 1-5 every 3 weeks until the end of month 6. 4. Vinblastine IV day 1 every 3 weeks until the end of month 6.

Group 1 "RISK" patients:

The primary aim of the study is to compare the therapeutic efficacy of control arm A (PDN+VBL) with the experimental arm B (PDN+VBL+MTX). The primary endpoint is the proportion of non-responder in risk organs to the initial treatment.

Non-response to initial therapy is defined as:

  • death within 12 weeks of initial treatment or
  • progression (worse) in risk organs at week 6
  • lack of response (=intermediate response or progression) in risk organs at week 12 as compared to the status of disease at week 6.

If the null hypothesis is true, the two randomized treatment arms are equally effective in terms of non-response. If the alternative hypotheses is true, there is a difference between the two randomized arms in terms of efficacy.

Group 2 "LOW RISK" patients:

The primary aim of the study is to compare the reactivation free survival rate in initial responders at week 6 with continuation treatment for 6 months (Arm LR 6) versus 12 months (Arm LR 12) in those patients without disease reactivation within the first 6 months.

If the null hypothesis is true, the reactivation rate of both randomized arms are equal. If the alternative hypothesis is true, there is a difference between the two arms in terms of reactivation frequency.

Therapy for "RISK" Patients:

Treatment A will consist of:

  1. Initial Therapy 8. Prednisone given by mouth three times a day daily as a four-week course, then gradually decreased over 2 more weeks.
  1. Vinblastine will be given IV (into a vein) one day a week for 6 weeks. 10. Patients who have no evidence of active disease at this time will proceed to continuation therapy.

Patients whose disease is improved or unchanged will receive additional therapy with:

  1. Prednisone in 3 divided doses by mouth for 3 days every week, from week 7-12.
  1. Vinblastine IV one day a week for 6 more weeks.

** If the disease is gone or better after this additional therapy continuation will begin.

Continuation Therapy:

  1. 6-MP by mouth daily until the end of month 12. 6. Prednisone in 3 doses daily day 1-5 every 3 weeks until the end of month 12. 7. Vinblastine IV day 1 every 3 weeks until the end of month 12.

** Those patients whose disease didn't respond to the initial therapy by the 12th week will come off this study and proceed to other research programs.

Treatment B will consist of:

  1. Initial Therapy
  2. Prednisone given by mouth three times a day daily as a four-week course then gradually decreased over 2 more weeks.
  3. Vinblastine will be given IV one day a week for 6 weeks.
  4. Methotrexate given as a 24 hour IV infusion day 1 of weeks 1, 3, and 5, followed by leucovorin.
  5. Leucovorin is a drug that will be given to help the body remove the methotrexate and decrease the possible side effects. (This is sometimes called a "leukovorin rescue". The drug will be given by mouth.)

    • Patients who have no evidence of active disease at this time will proceed to continuation therapy.

Patients whose disease is improved or unchanged will receive additional therapy with:

  1. Prednisone in 3 divided doses, days 1-3 weekly from week 7-12.
  2. Vinblastine IV one day a week for 6 more weeks.
  3. Methotrexate given as a 24 hour IV infusion day 1 of week 7, 9, and 11, followed by leucovorin.

    • If the disease is gone or better after this additional therapy continuation will begin.

Continuation Therapy:

  1. 6-MP by mouth daily until the end of month 12.
  2. Prednisone in 3 doses daily days 1-5 every 3 weeks until the end of month 12.
  3. Vinblastine IV day 1 every 3 weeks until the end of month 12.
  4. Methotrexate by mouth once weekly until the end of month 12.

Those patients whose disease didn't respond to the initial research program by the 12th week will come off this research study and proceed to another research program.

02

Conditions studied

03

In context

Histiocytosis, Langerhans-Cell

80 studies on the registry are indexed under Histiocytosis, Langerhans-Cell; 22 are open to participants now.

Browse Histiocytosis, Langerhans-Cell studies →

Lead sponsor

University of New Mexico is the lead sponsor of 306 studies on the registry; 28 are open to participants now.

Of its 25 completed or terminated interventional studies of FDA-regulated products, 23 (92%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

All newly diagnosed patients who meet the following criteria are eligible to be enrolled and followed in the study:

  • Definitive diagnosis of LCH
  • Age under 18 years
  • No prior treatment for LCH

Exclusion criteria

Exclusion Criteria:

  • Not specified
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Active comparator
    Treatment Arm A

    Drug: Prednisone, Vinblastin, 6-mercaptopuroine

  • Experimental
    Treatment Arm B

    Drug: Leucovorin, Methotrexate, Vinblastine, Prednisone

Interventions

  • DrugPrednisone, Vinblastin, 6-mercaptopuroine

    Initial Therapy:Prednisone- by mouth 3 times/day daily as a 4-week course, then gradually decreased over 2 more weeks. Vinblastine-IV (into a vein)1 day/week for 6 weeks. Patients w/o evidence of active disease at this time will proceed to continuation therapy. If disease is improved or unchanged, pts. will receive additional therapy with: Prednisone- 3 divided doses by mouth for 3 days every week, from week 7-12. Vinblastine- IV 1day/week for 6 more weeks. If the disease is gone or better after this additional therapy continuation will begin. Continuation Therapy: 6-MP:by mouth daily until the end of month 12. Prednisone in 3 doses daily day 1-5 every 3 weeks until the end of month 12. Vinblastine IV day 1 every 3 weeks until the end of month 12.

  • DrugLeucovorin, Methotrexate, Vinblastine, Prednisone

    Initial Therapy:Prednisone-by mouth 3x/day daily as a 4-week course then gradually decreased over 2 more weeks. Vinblastine- IV 1 day/week for 6 weeks. Methotrexate-a 24 hour IV infusion day 1 of weeks 1, 3, and 5, followed by leucovorin.The drug will be given by mouth. Pts w/o evidence of active disease at this time will proceed to continuation therapy. Pts whose disease is improved or unchanged will receive additional therapy w/:Prednisone- 3 divided doses, days 1-3 weekly from week 7-12. Vinblastine IV 1day/week for 6 more weeks. Methotrexate-a 24 hour IV infusion day 1 of week 7, 9, and 11, followed by leucovorin. If the disease is gone or better after this additional therapy continuation will begin. Continuation Therapy: 6-MP by mouth daily until the end of month 12. Prednisone- 3 doses daily days 1-5 every 3 weeks until the end of month 12. Vinblastine IV day 1 every 3 weeks until the end of month 12. Methotrexate by mouth once weekly until the end of month 12.

    Also known as: leukovorin rescue

06

What researchers measure

Primary outcomes

  1. The proportion of non-responder in risk organs to the initial treatment

    Time frame: 12 months

Secondary outcomes

  1. Overall survival

    Time frame: 12 months

  2. Proportion of responders (overall and in risk organs)

    Time frame: at week 6

  3. Proportion of responders (overall and in risk organs)

    Time frame: at week 12

  4. Reactivation free survival after response

    Time frame: at week 12

  5. Time to NAD

    Time frame: at weeks 6, 12, 7, or 13-23

07

Study locations

1 site
  • University of New Mexico
    Albuquerque, New Mexico 87131, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00488605
Lead sponsor
University of New Mexico
Responsible party
Sponsor
First posted
Jun 20, 2007
Start date
Aug 1, 2023
Primary completion
Aug 1, 2023
Completion
Aug 1, 2023
Last update
Aug 3, 2023

Study contacts

Jami Frost, M.D.
principal investigator · University of New Mexico

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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