Melphalan

Clinical trials are investigating Melphalan in several cancers and blood disorders. These studies look at safety, effectiveness, and longer-term outcomes in groups such as patients with multiple myeloma, leukemia, neuroblastoma, sarcoma, and metastatic cancer. The trials include different phases and treatment settings, including transplant preparation, consolidation therapy, and disease control.

Table of Contents

Clinical trials overview

These studies are looking at Melphalan in different cancer and transplant settings.[1] The trials are designed to test safety, treatment effect, and longer-term results in patients with blood cancers, solid tumors, and eye cancers.[1][2]

The trial designs are mostly interventional, which means the research team gives a treatment plan and measures the results.[1] The studies include both completed and authorised trials, with phases ranging from Phase 1/2 to Phase 4.[1][2]

Conditions studied with Melphalan

Melphalan appears in trials for several diseases, including multiple myeloma, acute myeloid leukemia, myelodysplastic syndrome, neuroblastoma, Ewing Sarcoma, retinoblastoma, metastatic colorectal cancer, metastatic breast cancer, uveal melanoma, and Langerhans Cell Histiocytosis.[1][2]

Some studies focus on disease that is high-risk, relapsed, refractory, or resistant, which means the cancer is harder to treat or has come back after earlier therapy.[1][2] Other trials look at Melphalan in transplant preparation or as part of consolidation treatment after the first phase of therapy.[1][2]

Who can take part

The target populations vary a lot from trial to trial.[1] Some trials include children and adolescents, such as studies in acute myeloid leukemia, neuroblastoma, retinoblastoma, and Langerhans Cell Histiocytosis.[1][2]

Other studies focus on adults with relapsed or refractory lymphoma, metastatic cancer, or blood cancers, and some are limited to older adults or people who are not eligible for autologous stem cell transplant.[1][2] Several transplant studies include patients with AML or MDS undergoing allogeneic transplantation or reduced intensity conditioning.[1]

Some trials also require a specific risk group, such as high-risk or very high-risk disease, or a specific disease state like first or second complete remission in AML.[1][2]

Trial phases and main endpoints

The phase of a trial shows how advanced the study is.[1] Phase 2 studies often look at safety and early signs of effect, while Phase 3 studies compare treatment strategies in larger groups.[1] The Phase 1/2 study in uveal melanoma is designed to find safe dosing and then test early efficacy.[1]

Common endpoints include overall survival, progression-free survival, event-free survival, and failure-free survival.[1][2] Some trials also measure toxicity, adverse events, serious adverse events, and specific disease response measures such as metastatic response or ocular preservation.[1][2]

For example, one Ewing Sarcoma study measures the frequency, duration, and severity of adverse effects and serious adverse effects, plus event-free survival at 36 months.[1] Another transplant study measures toxicity using the Bearman Scale and NCI CTCAE v5.0, and also looks at 2-year progression-free survival.[2]

How Melphalan is being used in the trials

Melphalan is usually part of a larger treatment plan rather than a stand-alone treatment.[1][2] In some trials it is used with other drugs such as fludarabine, treosulfan, busulfan, or cyclophosphamide in transplant conditioning, which means treatment given before stem cell transplant to prepare the body.[1][2]

In other studies, Melphalan is combined with chemotherapy, immunotherapy, or local procedures. Examples include high-dose regional treatment for liver-dominant metastatic disease, combination therapy in neuroblastoma, and intravitreal or intra-arterial use in retinoblastoma.[1][2]

Some studies compare one Melphalan-based strategy with another treatment strategy. For example, the RELEVANT trial compares treosulfan-based conditioning with Melphalan-based conditioning in AML and MDS, while the multiple myeloma trial in older adults compares standard treatment with experimental treatment plans that include Melphalan.[1][2]

Key studies at a glance

The largest studies in this data set are in neuroblastoma, acute myeloid leukemia, and precision medicine in cancer, but only some of them use Melphalan as a study drug.[1][2] The most direct Melphalan-focused trials include transplant conditioning studies, high-risk neuroblastoma studies, multiple myeloma studies, and studies of liver-dominant metastatic disease.[1][2]

  • High-risk Ewing Sarcoma study: tests Treosulfan/Melphalan consolidation and measures safety plus 36-month event-free survival.[1]

  • Transplant preparation study in AML or MDS: uses Melphalan with fludarabine and other agents, and measures toxicity and 2-year progression-free survival.[1]

  • RELEVANT trial: compares Melphalan-based conditioning with treosulfan-based conditioning in allogeneic transplant patients with AML or MDS, using overall survival as the main outcome.[1]

  • High-risk neuroblastoma phase 3 study: includes a Melphalan-containing high-dose chemotherapy arm and measures 3-year event-free survival.[1]

  • Retinoblastoma study: uses Melphalan by intra-arterial or intravitreal routes and measures eye preservation without external beam radiotherapy.[2]

  • Metastatic colorectal and breast cancer studies: test Melphalan-based liver-directed treatment followed by other systemic therapy and measure hepatic progression-free survival.[1][2]

Trial ID Phase Condition studied Status Enrollment
2024-518912-37-01 Phase 2 Ewing Sarcoma Authorised 60
2024-514483-11-00 Phase 2 High-Risk Myelodisplastic Syndrome or Acute Myeloid Leukemia Authorised 46
NCT07025824 Phase 2 AML and MDS undergoing allogeneic Transplantation Authorised 220
2024-514917-36-00 Phase 3 High-risk neuroblastoma Authorised 1060
NCT04802356 Phase 2 Multiple myeloma Completed 50
2024-520356-24-00 Phase 2 Refractory metastatic colorectal cancer with liver dominant disease Authorised 96
NCT03570892 Phase 3 Adult relapsed or refractory aggressive B-cell non-Hodgkin lymphoma Completed 348
2024-519089-32-02 Phase 2 Relapsed or resistant high-risk neuroblastoma Authorised 19
2023-503723-26-00 Phase 3 Allogeneic HSCT with reduced intensity conditioning Authorised 50
2022-500783-35-00 Phase 3 Acute Myeloid Leukemia in children and adolescents Authorised 1091
NCT03829371 Phase 3 Newly diagnosed multiple myeloma, transplant-ineligible or age 65+ Authorised 450
2024-516905-22-00 Phase 3 Newly diagnosed multiple myeloma Authorised 462
2024-517295-37-00 Phase 3 Low and intermediate risk neuroblastoma Authorised 280
2024-516127-14-01 Phase 1/2 Metastasized uveal melanoma Authorised 88
NCT02866136 Phase 2 Retinoblastoma Authorised 133

Ongoing Clinical Trials on Melphalan

  • Study of melphalan followed by eribulin, vinorelbine, or capecitabine versus eribulin, vinorelbine, or capecitabine alone for metastatic breast cancer patients with liver disease

    Recruiting

    1 1 1
    Investigated diseases:
    Italy Spain
  • Study of melphalan followed by trifluridine-tipiracil and bevacizumab combination versus trifluridine-tipiracil and bevacizumab in liver metastatic colorectal cancer

    Recruiting

    1 1 1
    Czechia Germany Italy The Netherlands Spain
  • Study Comparing Treosulfan and Melphalan with Fludarabine for Patients with Acute Myeloid Leukemia (AML) or Myelodysplastic Syndromes (MDS) Undergoing Transplantation

    Recruiting

    1 1 1
    Investigated diseases:
    Germany
  • Study on Stem Cell Transplantation and Immunotherapy with Rituximab, Dinutuximab Beta, and Drug Combination for Patients with High-Risk Relapsed Neuroblastoma

    Recruiting

    1 1 1
    Investigated diseases:
    Italy
  • Study on the Effectiveness of Tepotinib and Drug Combination for Patients with Advanced Cancer

    Recruiting

    1 1 1
    Norway
  • Study on Retinoblastoma Treatment Using Etoposide, Carboplatin, and Melphalan for Patients with Specific Eye Conditions

    Recruiting

    1 1 1
    France
  • Study on Fludarabine, Melphalan, and Radiation for Patients with High-Risk Myelodysplastic Syndrome or Acute Myeloid Leukemia Preparing for Stem Cell Transplant.

    Recruiting

    1 1 1
    Spain
  • Study on High-Risk Neuroblastoma Treatment with Busulfan, Melphalan, and Drug Combination for Patients with Insufficient Metastatic Response

    Recruiting

    1 1 1 1
    Austria Belgium Czechia Denmark France Germany +7
  • Study on Fludarabine, Melphalan, and ATG for Patients with Blood Cancer Undergoing Reduced Intensity Stem Cell Transplantation

    Recruiting

    1 1 1 1
    Investigated diseases:
    Belgium
  • Study on CAR-T-cell Therapy with Rituximab and Ibrutinib for Patients with High-Risk Mantle Cell Lymphoma

    Recruiting

    1 1 1
    Czechia France Germany The Netherlands Spain

Glossary

  • Phase: A stage of a clinical trial. Early phases usually focus on safety, while later phases often compare how well treatments work.
  • Interventional study: A trial where researchers give a treatment or treatment plan and then measure the results.
  • Enrollment: The number of participants planned or included in a study.
  • Overall survival (OS): The length of time from a study start point until death from any cause.
  • Progression-free survival (PFS): The length of time during and after treatment that a disease does not get worse.
  • Event-free survival (EFS): The length of time after treatment starts until a defined event happens, such as relapse, progression, a second cancer, or death.
  • Failure-free survival (FFS): The length of time after randomization until a treatment failure event happens, such as stable or progressive disease, or death.
  • Toxicity: Harmful effects of a treatment. In trials, this often means side effects that are measured and graded.
  • Adverse event (AE): Any unwanted medical problem that happens during a study.
  • Serious adverse event (SAE): A severe unwanted medical problem that can be life-threatening, need hospital care, or cause major harm.
  • Randomized: Participants are put into treatment groups by chance, so the groups can be compared fairly.
  • Conditioning regimen: Treatment given before a stem cell transplant to prepare the body for the transplant.

References

  1. https://clinicaltrials.gov/study/NCT00925782
  2. https://clinicaltrials.gov/study/NCT00582933
  3. https://clinicaltrials.gov/study/NCT00551928
  4. https://clinicaltrials.gov/study/NCT00176839
  5. https://clinicaltrials.gov/study/NCT00002730
  6. https://clinicaltrials.gov/study/NCT01323517
  7. https://clinicaltrials.eu/trial/study-comparing-bortezomib-melphalan-prednisone-lenalidomide-and-daratumumab-for-multiple-myeloma-in-patients-ineligible-for-stem-cell-transplant/
  8. https://clinicaltrials.gov/study/NCT00002630