Pregnancy outcome in chronic myeloid leukemia patients on imatinib therapy.

2013 ◽  
Vol 31 (15_suppl) ◽  
pp. 7114-7114
Author(s):  
Swati Dasgupta ◽  
Ashis Mukhopadhyay ◽  
Ujjal Kanti Ray ◽  
Firoj Hossain Gharami ◽  
Chinmay Kumar Basu ◽  
...  

7114 Background: Now that imatinib is being used to treat thousands of chronic myeloid leukemia (CML) patients for more than 10 year it is highly probable that many patients will get pregnant during its use. Company warns against any such use. But the fact remains that there is need for planned pregnancies in indicated cases. So we selected few cases both male and female for such pregnancies by interrupting treatment and following the pregnancy closely. Their outcome was studied so that we have an idea about what best could be suggested in such instance. Methods: From November 2002 to May 2010, 634 patients with CML in any stage of the disease were treated with imatinib at our tertiary cancer research institute. We selected 22 (12 females and 10 males) cases of pregnancies by interrupting treatment. We reported 9 accidental pregnancies and 13 planned pregnancies involving 22 patients who or their wives conceived while receiving imatinib for the treatment of CML. Results: Among 22 pregnancies there were 3 spontaneous abortions and 4 elective abortions. In case of 7 female patients, 3 and 4 were male and female babies respectably and in case of six male patients 4 and 4 were male and female babies. Two babies were with congenital anomaly such as one Hypospandium and one Mild-Hydrocephalus (in case of unplanned pregnancies and imatinib exposure during the first trimester of organogenesis). Conclusions: In conclusion, exposure to Imatinib during pregnancy might result in an increased risk of serious fetal abnormalities or spontaneous abortions. Women of childbearing potential should use adequate contraception while using Imatinib. We can suggest that planned pregnancy during therapy should be encouraged but imatinib therapy in unplanned pregnancy can cause spontaneous abortion or minor congenital anomaly.

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4493-4493
Author(s):  
Soma Mukhopadhyay ◽  
Ashis Mukhopadhyay ◽  
Swati Dasgupta ◽  
Subhasish Dey ◽  
Deboshree Majumdar ◽  
...  

Abstract Abstract 4493 Objective: Now that imatinib is being used to treat thousands of chronic myeloid leukemia (CML) patients for more than 10 year it is highly probable that many patients will get pregnant during its use. Company warns against any such use. But the fact remains that there is need for planned pregnancies in indicated cases. So we selected few cases both male and female for such pregnancies by interrupting treatment and following the pregnancy closely. Their outcome was studied so that we have an idea about what best could be suggested in such instance. Patients and Methods: From November 2002 to May 2010, 634 patients with CML in any stage of the disease were treated with imatinib at our tertiary cancer research institute. Among them 274 were female and 221 were of 17 to 50 years age group. We report information of 8 accidental pregnancies and 10 planned pregnancies involving 18 patients (10 females and 8 males) where pregnancy had occurred while receiving imatinib for the treatment of CML. Observations: Among 10 pregnancies reported in female sufferers there were two spontaneous and one elective abortion all in unplanned group and seven live births including one twin. There was one case of hypospadius which could be surgically corrected. Among the eight male patients whose wives conceived four pregnancies were planned, there was one spontaneous abortion, two elective abortions. The conceptions resulted in the birth of five healthy babies (two females). There was no other identifiable congenital anomaly. Conclusion: In the patients, who do become pregnant while on treatment, balancing the risk to the fetus of continuing imatinib versus the risk to the mother of interrupting treatment remains difficult. From the fetal perspective, imatinib should be discontinued due to the potential risk of serious developmental abnormalities; from the maternal perspective also there is chance of drug interruption induced cytogenetic relapse. CML patients, in the child bearing age group can do bear children. There was no major foetal anomalies which was documented. In the case of female patients the drug was withheld during the first trimester for concerns regarding potential teratogenecity. In both male and female, in the case of a planned pregnancy the drug should preferably be stopped one month before the time of expected conception. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 4885-4885
Author(s):  
Kleber Matias ◽  
Carolina Matias ◽  
Ana Dulce Freire ◽  
Alita Andrade Azevedo

Abstract The occurrence of leukemia during pregnancy is very rare with an estimated incidence of one per 100,000 pregnancies annually. It has been estimated that during pregnancy most leukemias are acute: two thirds are myeloid (AML) and one third are lymphoid (ALL). Chronic myeloid leukemia (CML) is found in less than 10% of leukemias during pregnancy and chronic lymphocytic leukemia (CLL) is extremely rare. The management of CML during pregnancy is a difficult problem because of the potential effects of the therapy on the mother and fetus. Since the disease has an initial chronic phase, it is usually managed conservatively during pregnancy, while an aggressive approach, such as bone marrow transplantation, may be considered after delivery. A limited number of cases described successful treatment modalities of CML during pregnancy including leukapheresis, hydroxyurea (HU) and interferon (IFN). We report nine cases of pregnancy in seven chronic myeloid leukemia patients, giving birth healthy children in a single institution from 1979 to 2005. In four cases the diagnosis of CML was made on prebirth period in routine blood testing, and five pregnancies developed during the course of disease. Four of the pregnancies were found in the first trimester, four in the second and one in the third. Median age of patients was 21 years (range 18–30years). All patients were Ph1 positive and the leucocyte count ranged between 45 to 336 x 109 /L. Table 1 shows treatment performed in patients before and during pregnancy. Patients 4 and 7 had a subsequent pregnancy despite the use of contraceptive methods, both diagnosed in the first trimester. Hydroxyurea was stopped during pregnancy. Delivery was performed by caesarean section in 5 cases and by spontaneous vaginal delivery in 4 cases. All infants’ examination and blood counts were normal and there were no perinatal or maternal complications. In june 2005, two new cases of pregnant CML patients were seen at our institution. One of them was being treated with imatinib, and the other without treatment at the moment of pregnancy. They will be managed only with leukapheresis. Our data suggest that exposure to IFN and HU during pregnancy is probably not associated with a significantly increased risk for malformations, however leukapheresis can be considered for treatment of CML during pregnancy because of the lack of teratogenic and other adverse effects in patients who tolerate and respond to the procedure. Cases Age (years) CML diagnosis Pregnancy diagnosis Trimester of pregnancy Treatment before pregnancy Treatment during pregnancy 1 18 Sep/1993 Oct/1993 First None HU 2 30 Dec/1996 Jan/1997 Third None Leukapheresis 3 18 Dec/1993 Nov/1995 First IFN stopped IFN 4 21 Sep/1995 Sep/1995 Second None HU 5 21 Jul/1994 Aug/1994 Second HU stopped HU 6 27 Jan/1979 Jan/1979 Second None Busulphan - 2 months 7 18 Dec/1995 Oct/1996 Second HU HU


Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 2948-2948
Author(s):  
Mario Tiribelli ◽  
Antonio Colatutto ◽  
Luciana Marin ◽  
Eleonora Toffoletti ◽  
Giuseppe Barbina ◽  
...  

Abstract In the last year, the issue of cardiotoxicity of imatinib mesylate (IM) was on focus. Emerging data seem to deny an increased risk of cardiac events in patients treated with IM, which is the frontline therapy in chronic myeloid leukemia (CML). B-type natriuretic peptide (BNP) is released by the heart in response to myocardial tension and is considered an accurate test for the diagnosis of heart failure. The measurement of BNP in the serum is a rapid and easy tool for evaluation of ventricular function, also in asymptomatic patients. We have measured BNP level in 50 consecutive patients (33 males and 17 females) with IM treated chronic phase CML. Patients were enrolled, after informed consent was obtained, as they presented for a follow-up visit at our Institution. BNP was measured using a direct chemiluminescent sandwich immunoassay: the analytical range extends from 0 to 5000 pg/ml, with a sensitivity <2 pg/ml. Normal range is as follows: <100 pg/dl. Median age was 59 (range: 23–82). Median duration of IM therapy was 38.5 months (range: 1–81). IM mean daily dose at time of sample collection was 404 mg (SD ±121). Thirty three patients (66%) were receiving 400 mg/day, 13 (26%) a lower daily dose (200 mg in 1 case, 300 mg in 12) and 5 patients (10%) had higher IM doses (600 mg in 2, 800 mg in 3). The mean level of BNP in the whole population was 22.0 pg/ml (SD ±26.4); only two patients had values >100 pg/ml. There was a linear correlation between age and BNP levels (t–value=3.850, p=0.0003). Nine out of 24 (37%) patients aged ≥60 had BNP >22 pg/ml, compared to only 1/25 (4%) in the cohort <60 years old (χ2=19.7, p<0.0001). BNP level was not affected by IM daily dose (<400 mg = 34.1±28.6, 400 mg = 18.5±26.2, >400 = 13.5±9.3) or by therapy duration (<36 months = 25.2±30.4, ≥36 months = 19.4±22.6). Considering cardiovascular risk factors, 18 patients (36%) had hypertension, while diabetes and hyperlipemia were present in 2 and 4 cases, respectively. Patients with hypertension had higher levels of BNP (34.9±35.1 vs 14.8±16.5, p=0.03), despite an equivalent IM dose (378±81 vs 419±138 mg) and treatment duration (39.5 vs 30.5 months). No patient experienced major cardiac adverse event during IM therapy. An echocardiogram was performed in the two patients with higher BNP values: both of them were older than 60 and suffered from hypertension, but echocardiogram revealed a normal left ventricular ejective function (LVEF ≥65%). To further assess IM impact on BNP levels, five consecutive patients, who were diagnosed with CML during study period, were tested for BNP before start of IM therapy and after 1, 2 and three months of therapy. No significant modification in BNP level was observed during treatment with IM. In conclusion, Imatinib therapy does not cause an increase in BNP levels. This gives an indirect confirm to the cardiac safety profile of the drug, as indicated also by the lack of major cardiac toxicities in our patients. BNP levels were affected by hypertension and by advanced age, but the latter could be a bias due to a higher incidence of hypertension in the elderly cohort.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 4613-4613
Author(s):  
Mohammad Abu-Tineh ◽  
Elrazi Awadelkarim A Ali ◽  
Awni Alshurafa ◽  
Khalid Alhaj ◽  
Yousef Hailan ◽  
...  

Abstract Introduction Following the launch of the TKI's (tyrosine kinase inhibitors) for the treatment of CML (Chronic myeloid leukemia), establishing its significant control over the disease as evident by multiple studies such as the population based Swedish CML registry reporting that Patients reaching 70 years of age had a relative survival close to 1.0 compared to the normal population with the same age. Consequently, other dimensions have emerged regarding the safety of treatment, particularly the effect on Male fatherhood. This study was conducted to review the real-life data on the effect of TKI on the fatherhood of male patients in the National Center of cancer care and research (NCCCR) in Qatar in the period of 1st of January 2005 - 1st of January 2020. Up to our knowledge, this is the first study addressing the effect of TKI on fatherhood in patients with CML. Methods A single-center study, conducted a mixed-design (retrospective+ phone interviews) with CML male patients in the Chronic or accelerated phase, being followed up in NCCCR, evaluating the effect of Imatinib, Dasatinib, nilotinib, on their fatherhood whether they are taking it as first, a second, or third line of treatment. Inclusion Criteria: -Male patient diagnosed with CML, in Chronic or accelerated phase; 18 years of age or older and actively receiving tyrosine kinase inhibitors including (Imatinib, dasatinib, nilotinib) with the following: -Patients with no known issues with regards to fertility, (fertility is intact) will be included in the study. -Patients who developed fertility issues after the diagnosis of CML and starting TKI's. He has been evaluated by an andrologist and his evaluation concluded its TKI related. Exclusion criteria: -Patients with other MPNS. -Patients not fulfilling inclusion criteria as follow: -Patient known to have infertility before the diagnosis of CML -Patient with infertility after Diagnosis of CML: If a clear underlying cause, not TKI related, will be excluded from the studyif no evaluation was done for infertility and it is not clear whether the infertility is related to an underlying cause or TKI and no proper evaluation by andrologist done excluded from this study The mother has documentation by gynecologist for infertility, or after examining the abortion, still-birth, or IUFD and checking the chromosomal analysis (any mother related cause whether endogenous or exogenous has been excluded) Results: 150 patients were interviewed to be included in the study, 22 (14%) patients had concerns related to medications safety and possible transmission of the disease, 33 (22%) patients had their families completed by the time of diagnosis. 26 patients have met the inclusion criteria, median age around 44 years, median age at diagnosis was 33.5. 100% were in chronic phase, 42.3% were on imatinib, 34.6% on Nilotinib, and 23.1% on Dasatinib. The median TKI exposure period before pregnancy was 3 years. Median age at first conception post TKI treatment is 36, with a median duration of TKI treatment around 7 years. offspring's total number was 43, 97.6% were full-term, had a normal delivery, and normal average weight at delivery. No stillbirths, fetal demise, or congenital anomaly were reported. All offspring had normal development and growth. Median age of children after CML diagnosis around 7 years. No reports of any CML-related cancer in all the offspring Conclusion: Around 98% of male CML patients taking imatinib, Dasatinib, Nilotinib had their offspring born normally with no delivery complications noted, all had no congenital anomaly, had normal growth and development, and no CML-related cancers were diagnosed. Further studies with a larger sample size are required to shed light on the TKI outcome on fatherhood in CML patients. Nonetheless, a call for attention for better education to patients starting on TKI's addressing the possible psychological fear or concerns of having an unsatisfactory effect on their fertility/offspring, targeting better acceptance and adherence to treatment. Figure 1 Figure 1. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2009 ◽  
Vol 113 (25) ◽  
pp. 6315-6321 ◽  
Author(s):  
Alfonso Quintás-Cardama ◽  
Hagop Kantarjian ◽  
Dan Jones ◽  
Jianqin Shan ◽  
Gautam Borthakur ◽  
...  

AbstractPatients not in complete cytogenetic response (CCyR) continuously face the competing possibilities of eventually achieving a cytogenetic response versus progressing. We analyzed the probability of achieving a CCyR, major molecular response, and progression in 258 patients with chronic myeloid leukemia in early chronic phase at 3, 6, and 12 months from imatinib start. The initial imatinib dose was 800 mg/day in 208 (81%) and 400 mg/day in 50 (19%) patients. For patients not in CCyR, the probability of achieving CCyR (P = .002) or major molecular response (P = .004) significantly decreased, whereas the risk of progression increased (P = .16) at each time point. Patients with a BCR-ABL1/ABL1 ratio greater than 1% to 10% after 3 months of imatinib had a 92% probability of achieving CCyR with continued therapy, similar to the 98% for those with 1% or less, but their risk of progression (11%) was almost 3-fold that of patients with a BCR-ABL1/ABL1 transcript ratio of 1% or less (4%) and similar to that of patients with transcript levels more than 10% (13%). These results suggest that patients not in CCyR after 12 months on imatinib have a higher risk of progression. This risk is discernible as early as 3 months into imatinib therapy by molecular analysis and may provide the rationale to institute therapies that render higher rates of early response.


2019 ◽  
Vol 11 (1) ◽  
pp. 27-33
Author(s):  
I Dmytrenko ◽  
J Minchenko ◽  
I Dyagil

The chronic myeloid leukemia (CML) development is associated with the formation of the BCR/ABL1 fusion gene and the BCR/ABL1 protein with increased tyrosine kinase activity. Despite the high efficiency of targeted therapy, up to 30% of patients do not respond on such therapy i.e. are primary resistant. The presence of BCR/ABL1 kinase domain mutations is considered to be one of the reasons of tyrosin kinase inhibitors resistance. To evaluate the frequency of BCR/ABL1 kinase domain mutations in Ukrainian cohort of CML patients with primary resistance to imatinib therapy, we retrospectively studied BCR/ABL1 kinase domain mutations in peripheral blood of 107 CML patients. The nucleotide sequence was determined by direct sequencing by Sanger. Mutations were reported in 45 of 107 (41.7%) CML patients. Two mutations at a time were revealed in 8 patients. So a total of 53 mutations were found out. Among them 49 were missense-mutations and 4 - deletions of different regions of the BCR/ABL1 kinase domain gene. The missense-mutations F359I/V (12 patients), T315I (8 patients) and G250E (6 patients) were most common. By localization, the mutations majority (23 of 53) was in the P-loop, 10 mutations - in the contact site, 13 mutations - in the catalytic domain and 6 – in the A-loop. Of the detected mutations, 26 (49%) resulted in a disruption of the hydrogen bond between BCR/ABL1-tyrosine kinase and imatinib. Significant reduction in overall survival was found in patients with BCR/ABL1 kinase domain mutations compared with patients with wild-type of BCR/ABL1 gene (p=0.018). The estimated 3-year overall survival was 83.4% (95% CI: 77.0%-89.8%) and 94.3% (95% CI: 91.0%-97.3%), respectively. Therefore, mutations of the BCR/ABL1 kinase domain are one of the mechanisms of primary resistance in CML patients on imatinib therapy. The occurrence of BCR/ABL1 gene mutations impairs the prognosis of imatinib therapy response.


2017 ◽  
Vol 17 (10) ◽  
pp. 696-702
Author(s):  
Irena Ćojbašić ◽  
Lana Mačukanović-Golubović ◽  
Miodrag Vučić ◽  
Ivan Tijanić

Blood ◽  
2009 ◽  
Vol 114 (2) ◽  
pp. 261-263 ◽  
Author(s):  
Alfonso Quintás-Cardama ◽  
Xin Han ◽  
Hagop Kantarjian ◽  
Jorge Cortes

Abstract Dasatinib is associated with increased risk of bleeding among patients with chronic myeloid leukemia, even in the absence of thrombocytopenia, suggesting the presence of a hemostatic defect. We tested platelet aggregation in 91 patients with chronic myeloid leukemia in chronic phase either off-therapy (n = 4) or receiving dasatinib (n = 27), bosutinib (n = 32), imatinib (n = 19), or nilotinib (n = 9). All but 3 patients simultaneously receiving imatinib and warfarin had normal coagulation studies. All 4 patients off therapy had normal platelet aggregation. Impaired platelet aggregation on stimulation with arachidonic acid, epinephrine, or both was observed in 70%, 85%, and 59% of patients on dasatinib, respectively. Eighty-five percent of patients on bosutinib, 100% on nilotinib, and 33% on imatinib had normal platelet aggregation. Dasatinib 400 nM induced rapid and marked prolongation of closure time to collagen/epinephrine in normal whole blood on the PFA-100 system. In conclusion, dasatinib and, to some extent, imatinib produce abnormalities in platelet aggregometry testing.


2016 ◽  
Vol 49 (8) ◽  
pp. 553-558
Author(s):  
Kotoko Yamatani ◽  
Hayato Mikami ◽  
Tetsuya Yoshikura ◽  
Sachiyo Osawa ◽  
Yoshihiro Takami ◽  
...  

2015 ◽  
Vol 4 (6S) ◽  
pp. 13-16
Author(s):  
Fausto Palmieri

Here we describe a case of a young patient with chronic myeloid leukemia, at high-risk according to the Sokal index, who started imatinib at standard dose and obtained a sub-optimal response at 12 months. This condition was not automatically an indication to change therapy, but considering the patient as suboptimal, we decided to switch to a second-generation tyrosine kinase inhibitor (TKI), nilotinib 800 mg/die, obtaining soon a complete cytogenetic response (CCYR), thereafter a major molecular response (MMolR). Delayed achievement of cytogenetic and molecular is associated with increased risk of progression among patients with chronic myeloid leukemia in early chronic phase receiving imatinib therapy. Therefore we can hypothesise that this kind of patient could be elegible for an early switch to second-generation TKI.


Sign in / Sign up

Export Citation Format

Share Document