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Myeloma VII - myelomatosis therapy trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN66518389
Enrollment
750
Registered
2000-10-25
Start date
1993-09-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Leukaemia Cancer Leukaemia

Interventions

ABCM for plateau induction with alpha Interferon (IFN) maintenance/a three-phase regimen of C-VAMP, high dose melphalan (with autologous bone marrow/peripheral blood stem cell support as appropriate)

Sponsors

Medical Research Council (MRC) (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. They have definite myelomatosis requiring chemotherapy and fulfilling at least two of the three following criteria: bone marrow aspirate and/or trephine showing the presence of a neoplastic plasma cell infiltrate and/or microplasmacytomas, a paraprotein present in blood and/or urine 2. They have definite lytic bone lesions 3. They are aged under 65 years 4. They are able to tolerate a daily fluid intake of not less than 3 litres 5. The physician is satisfied it would be appropriate to receive any of specified treatments

Exclusion criteria

Exclusion criteria: 1. Patients have equivocal myelomatosis (these should be registered but will not receive treatment - if disease progresses then they may be entered into the main trial) 2. They have previous malignancies except non-melanoma skin tumours or in situ carcinomas 3. Had previous treatment except minimal local radiotherapy to relieve bone pain 4. If have a life threatening disease unrelated to myelomastosis.

Design outcomes

Primary

MeasureTime frame
Overall survival

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026