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Enrolling by Invitation

NCT Number: NCT04210791

Autologous Stem Cell Transplantation for Patients With AL Amyloidosis

This study mainly evaluated the efficacy and safety of autologous stem cell transplantation for the treatment of AL amyloidosis, the role of induction and maintenance therapy in autologous stem cell transplantation, and the long-term efficacy and prognosis risk factors of autologous stem cell transplantation for the treatment of AL amyloidosis.

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Key information

About this study

This study is divided into two parts. In the first part, the investigators retrospectively analyze the data of patients with AL amyloidosis who treated with autologous stem cell transplantation from July 2010 to December 2019. All patients had a biopsy-proven disease by positive Congo red stain with a concomitant demonstration of plasma cell dyscrasia. Organ involvement was established according to the criteria established at the 10th International Symposium on Amyloid and Amyloidosis. The protocol of ASCT included mobilization with colony-stimulating factor alone and conditioning with high-dose melphalan 140 or 200 mg/m2. In addition to analyzing the efficacy and safety of all the patients, the investigators also analyzed the difference in efficacy between patients in different subgroups. For example, subgroups divided according to different induction treatment regimens; subgroups divided according to different plasma cell FISH data and FCM data; subgroups divided according to the degree of organ involvement, and subgroups divided according to different maintenance treatment regimens.

In the second part of the study, the investigators will conduct a prospective study to explore the best autologous stem cell transplantation treatment protocol for AL amyloidosis. The protocol includes the induction therapy with bortezomib and daratumumab before ASCT, the maintenance treatment with lenalidomide after ASCT, and the treatment options for recurrence after transplantation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female;
  • aged 18-75 years;
  • Patients with newly diagnosed AL;
  • Appropriate for autologous hematopoietic stem cell transplantation;
  • Abnormal M protein or free light chain detected in serum and/or urine
  • ECOG score 0-2 points;
  • Subjects (or their legal representatives) must sign an informed consent document indicating understanding the purpose of and procedures required for the study and willingness to participate in the study.

Exclusion criteria

  • Pregnant and breastfeeding women;
  • Subjects suffering from multiple myeloma;
  • hypersensitivity to any treatment drugs;
  • Subjects have severe cardiovascular disease;
  • Subjects have a serious physical disease and mental illnesses;
  • Other conditions that researchers consider are not suitable for transplantation.

Treatment and study plan

Primary outcomes

  1. overall survival

    Time frame: 5 years

    the 5 years overall survival after autologous stem cell transplantation.

  2. progression-free survival

    Time frame: 5 years

    the 5 years progression-free survival after autologous stem cell transplantation.

  3. hematological complete response rate

    Time frame: 1 year

    the 1 year hematologic complete response rate after autologous stem cell transplantation.

  4. organ response rate

    Time frame: 1 year

    the 1 years organ response rate after autologous stem cell transplantation.

Secondary outcomes

  1. hematological overall response rate

    Time frame: 1 year

    the 1 years hematologic overall response rate after autologous stem cell transplantation.

  2. the relapse rate of complete remission participants

    Time frame: 5 years

    the relapse rate of complete remission participants after autologous stem cell transplantation.

  3. the rate of Minimal Residual Disease-negative participants

    Time frame: 5 years

    the rate of Minimal Residual Disease-negative participants after autologous stem cell transplantation.

  4. the median time form stem cell transplantation to next treatment

    Time frame: 5 years

    the median time form stem cell transplantation to next chemotherapy or antibody treatment.

Sponsors and collaborators

Lead sponsor

Nanjing University School of Medicine

Other

Registry information

Important dates

Study start
2010
Primary completion
2025
Study completion
2030
First posted
Dec 26, 2019
Registry last updated
Feb 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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