About this trial
Before effective treatment, the prognosis of patients with AL amyloidosis is very poor, with a median survival of approximately 12 months. In recent decades, with the development of new drugs, the treatment paradigm for AL amyloidosis has undergone significant changes, and the prognosis has improved dramatically. Achieving very good partial response (VGPR) or even complete response (CR) can lead to higher organ response and longer survival. However, not all patients who achieve ≥VGPR reach organ response, which may be related to the presence of small residual plasma cell clones in these patients. The ongoing production of monoclonal light chains deposits into tissues and organs, causing continuous damage, making organ response difficult. With the development of new drugs, the rate of hematologic CR has continuously increased, and the advancement of minimal residual disease (MRD) detection technologies in recent years has led to increasing attention to MRD in AL amyloidosis research. Therefore, in this era of advancing new drugs, MRD negativity may become a higher clinical treatment goal for AL amyloidosis, further improving long-term prognosis for patients.
Our department plans to conduct a single-center, prospective clinical study aimed at exploring the MRD status in patients who achieve hematologic CR after first-line induction chemotherapy (Dara-CyBorD), and further investigating whether autologous stem cell transplantation in MRD-positive CR patients who meet transplant criteria can further improve organ response, progression-free survival, and overall survival.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age range: 18-70 years (inclusive), no gender restriction;
Newly diagnosed AL amyloidosis patients;
Meet ASCT eligibility criteria and have a willingness to undergo ASCT;
Achieved hematological complete response (CR) after 2-4 cycles of Dara-CyBorD induction chemotherapy.
Disqualifiers
Secondary to multiple myeloma or lymphoplasmacytic lymphoma, such as Waldenström's macroglobulinemia;
Co-existing other active malignant tumors;
Co-existing other systemic diseases deemed unsuitable for inclusion by the investigator, such as newly developed severe cardiovascular and cerebrovascular diseases, or severe infections.
Trial design
Single group
Treatments tested in this trial
First-Line Dara-BorCyD Treatment
DrugFirst-Line Dara-BorCyD Treatment Achieves CR, but ASCT is Recommended for MRD-Positive Patients
Treatment groups
Trial outcomes
Primary outcomes
Organ Response Rates
Progression-Free Survival
Overall Survival
Sponsors and contacts
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Peking University First Hospital
Lead sponsor
Beijing Chao Yang Hospital
Collaborator
Beijing Anzhen Hospital
Collaborator