Treatment of M3 type leukemia?
Hello Dr.
Hu,
I am currently a patient with M3 type leukemia.
My treatment phase involves daily oral all-trans retinoic acid and two phases of arsenic trioxide injections (7 days each phase for a total of 14 days).
After about a month of monitoring, my blood cell counts have generally returned to standard values, and the computer count shows zero abnormal cells.
Starting next week, I will undergo a bone marrow examination and enter the next phase of consolidation treatment with arsenic trioxide injections (expected to be 4 phases).
My question is, if during the consolidation treatment (after the bone marrow examination shows no abnormal cells), is it still necessary to complete all 4 phases? Or can I stop? Thank you.
Fred, 50~59 year old female. Ask Date: 2024/03/17
Dr. Hu Ziren reply Oncology
Patients with M3-type leukemia, in addition to the initial induction therapy and subsequent consolidation therapy, often undergo maintenance therapy for 1-2 years.
Although M3-type leukemia has a relatively favorable prognosis among acute leukemias, approximately 5% of patients may experience relapse, and the risk of relapse is higher in high-risk patients.
Therefore, it is recommended to adhere to the physician's advice and complete the planned treatment regimen.
Reply Date: 2024/03/17
More Info
In the context of M3 leukemia, also known as acute promyelocytic leukemia (APL), the treatment protocol typically involves several phases, including induction therapy, consolidation therapy, and sometimes maintenance therapy. Your current treatment regimen, which includes all-trans retinoic acid (ATRA) and arsenic trioxide (ATO), is standard for APL and has shown significant efficacy in achieving remission.
Consolidation therapy is a critical component of the treatment plan for APL. Even if your bone marrow examination shows no detectable leukemic cells (i.e., a complete remission), it is essential to complete the planned consolidation therapy. The rationale behind this is that while you may currently be in remission, there is still a risk of residual disease that may not be detectable through standard testing methods. Studies have shown that completing the full course of consolidation therapy significantly reduces the risk of relapse.
In APL, the risk of relapse can be influenced by several factors, including the initial response to treatment, the presence of certain genetic markers, and the overall health of the patient. Although APL has a favorable prognosis compared to other types of acute myeloid leukemia (AML), approximately 5-10% of patients may experience a relapse, particularly if consolidation therapy is not completed. For high-risk patients, the relapse rate can be even higher.
The consolidation phase typically involves multiple cycles of ATO, which is administered over several weeks. This phase aims to eliminate any remaining leukemic cells and to solidify the remission achieved during the induction phase. Stopping treatment prematurely, even if you feel well and your blood counts are normal, could leave you vulnerable to a relapse, which may be more challenging to treat.
Furthermore, the treatment landscape for APL has evolved, and ongoing research continues to refine the best practices for consolidation and maintenance therapy. Some studies suggest that additional therapies, such as maintenance with ATRA or other agents, may further improve long-term outcomes.
In summary, it is strongly advised to follow your physician's recommendations and complete the planned consolidation therapy, even if your current bone marrow examination shows no evidence of disease. This approach maximizes your chances of achieving a durable remission and minimizes the risk of relapse. Always discuss any concerns or questions with your healthcare team, as they can provide personalized guidance based on your specific situation and treatment response.
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