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Before the era of 2nd generation TKIs, several intervention trials were designed to optimized and possibly increased imatinib efficacy. The SPIRIT French trial was one of them and enrolled front-line chronic-phase chronic myeloid leukemia (CML) patients in a four-arm study comparing imatinib (IM) 400 mg versus IM 600 mg, IM 400 mg + cytarabine (AraC), and IM 400 mg + pegylated interferon alpha2a (PegIFN-α2a). Few trials in CML had a long term follow up pass the 10 years, so the French group recently reported the results based on intention-to-treat analyses, at 15 years. The overall and progression-free survival were similar across all arms. As previously documented by the German IV study the combination of IM + PegIFN-α2a had an earlier higher rate of molecular response but did not translate into better survival and PFS for this arm. Regarding TFR, the proportion of patients still in response without restarting treatment was similar in the IM 400 mg arm and the IM + PegIFN-α2a arm, 40% and 38%, respectively.
Although TFR is a reality on today's management of CML patients, it is important to emphasize a proper molecular monitoring after TKI discontinuation following the current NCCN and ELN guidelines. However, late relapses may occur after one year of therapy, although there are uncommon. In a recent letter to the editor in the journal Leukemia, investigators that participated in the EURO-SKI trial planned to follow patients beyond the 3 years scheduled in the trial and they reported the outcomes in what they called the AFTER-SKI trial. With a follow-up of 72 months, 12 out of 111 patients (10.8%) who were in TFR at 36 months, subsequently lost MMR. What is interesting is that the molecular status at 36 months appears highly predictive of later relapse, as only 1 patient out of 98 in MR4 at month 36 lost MMR in the following 3 years. Conversely, 11 of the 13 patients not in MR4 at month 36 lost MMR during follow-up.
For older CML patients not eligible for TFR or after TFR failure, long term therapy with TKI is the only option. However, we know that many patients can suffer from chronic AEs that will impact long term quality of life. A recent publication of the Italian phase III multicentric randomized OPTkIMA study aimed to evaluate if a progressive de‐escalation of TKIs was able to maintain the molecular response (MR3.0) and improve Health Related Quality of Life (HRQoL). 166 elderly CML patients in stable MR3.0/MR4.0completed the first year of any TKI intermittent schedule, 1 month ON and 1 month OFF. The first-year probability of maintaining the MR3.0 was 81%. No patients progressed to accelerated/blastic phase. All patients who lost the molecular response regained the MR3.0 after resuming TKI continuously, and none suffered from TKI withdrawn syndrome. However, data related with quality of life was confounded by several factors and non-conclusive, for which longer follow up will be needed.
Before the era of 2nd generation TKIs, several intervention trials were designed to optimized and possibly increased imatinib efficacy. The SPIRIT French trial was one of them and enrolled front-line chronic-phase chronic myeloid leukemia (CML) patients in a four-arm study comparing imatinib (IM) 400 mg versus IM 600 mg, IM 400 mg + cytarabine (AraC), and IM 400 mg + pegylated interferon alpha2a (PegIFN-α2a). Few trials in CML had a long term follow up pass the 10 years, so the French group recently reported the results based on intention-to-treat analyses, at 15 years. The overall and progression-free survival were similar across all arms. As previously documented by the German IV study the combination of IM + PegIFN-α2a had an earlier higher rate of molecular response but did not translate into better survival and PFS for this arm. Regarding TFR, the proportion of patients still in response without restarting treatment was similar in the IM 400 mg arm and the IM + PegIFN-α2a arm, 40% and 38%, respectively.
Although TFR is a reality on today's management of CML patients, it is important to emphasize a proper molecular monitoring after TKI discontinuation following the current NCCN and ELN guidelines. However, late relapses may occur after one year of therapy, although there are uncommon. In a recent letter to the editor in the journal Leukemia, investigators that participated in the EURO-SKI trial planned to follow patients beyond the 3 years scheduled in the trial and they reported the outcomes in what they called the AFTER-SKI trial. With a follow-up of 72 months, 12 out of 111 patients (10.8%) who were in TFR at 36 months, subsequently lost MMR. What is interesting is that the molecular status at 36 months appears highly predictive of later relapse, as only 1 patient out of 98 in MR4 at month 36 lost MMR in the following 3 years. Conversely, 11 of the 13 patients not in MR4 at month 36 lost MMR during follow-up.
For older CML patients not eligible for TFR or after TFR failure, long term therapy with TKI is the only option. However, we know that many patients can suffer from chronic AEs that will impact long term quality of life. A recent publication of the Italian phase III multicentric randomized OPTkIMA study aimed to evaluate if a progressive de‐escalation of TKIs was able to maintain the molecular response (MR3.0) and improve Health Related Quality of Life (HRQoL). 166 elderly CML patients in stable MR3.0/MR4.0completed the first year of any TKI intermittent schedule, 1 month ON and 1 month OFF. The first-year probability of maintaining the MR3.0 was 81%. No patients progressed to accelerated/blastic phase. All patients who lost the molecular response regained the MR3.0 after resuming TKI continuously, and none suffered from TKI withdrawn syndrome. However, data related with quality of life was confounded by several factors and non-conclusive, for which longer follow up will be needed.
Before the era of 2nd generation TKIs, several intervention trials were designed to optimized and possibly increased imatinib efficacy. The SPIRIT French trial was one of them and enrolled front-line chronic-phase chronic myeloid leukemia (CML) patients in a four-arm study comparing imatinib (IM) 400 mg versus IM 600 mg, IM 400 mg + cytarabine (AraC), and IM 400 mg + pegylated interferon alpha2a (PegIFN-α2a). Few trials in CML had a long term follow up pass the 10 years, so the French group recently reported the results based on intention-to-treat analyses, at 15 years. The overall and progression-free survival were similar across all arms. As previously documented by the German IV study the combination of IM + PegIFN-α2a had an earlier higher rate of molecular response but did not translate into better survival and PFS for this arm. Regarding TFR, the proportion of patients still in response without restarting treatment was similar in the IM 400 mg arm and the IM + PegIFN-α2a arm, 40% and 38%, respectively.
Although TFR is a reality on today's management of CML patients, it is important to emphasize a proper molecular monitoring after TKI discontinuation following the current NCCN and ELN guidelines. However, late relapses may occur after one year of therapy, although there are uncommon. In a recent letter to the editor in the journal Leukemia, investigators that participated in the EURO-SKI trial planned to follow patients beyond the 3 years scheduled in the trial and they reported the outcomes in what they called the AFTER-SKI trial. With a follow-up of 72 months, 12 out of 111 patients (10.8%) who were in TFR at 36 months, subsequently lost MMR. What is interesting is that the molecular status at 36 months appears highly predictive of later relapse, as only 1 patient out of 98 in MR4 at month 36 lost MMR in the following 3 years. Conversely, 11 of the 13 patients not in MR4 at month 36 lost MMR during follow-up.
For older CML patients not eligible for TFR or after TFR failure, long term therapy with TKI is the only option. However, we know that many patients can suffer from chronic AEs that will impact long term quality of life. A recent publication of the Italian phase III multicentric randomized OPTkIMA study aimed to evaluate if a progressive de‐escalation of TKIs was able to maintain the molecular response (MR3.0) and improve Health Related Quality of Life (HRQoL). 166 elderly CML patients in stable MR3.0/MR4.0completed the first year of any TKI intermittent schedule, 1 month ON and 1 month OFF. The first-year probability of maintaining the MR3.0 was 81%. No patients progressed to accelerated/blastic phase. All patients who lost the molecular response regained the MR3.0 after resuming TKI continuously, and none suffered from TKI withdrawn syndrome. However, data related with quality of life was confounded by several factors and non-conclusive, for which longer follow up will be needed.