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Objectives: To determine the long term outcome after intracoronary β radiation therapy (IRT).
Setting: Tertiary referral centre.
Methods: The rate of major adverse cardiac events (MACE) was retrospectively determined in 301 consecutive patients who were treated with IRT. MACE was defined as death, myocardial infarction, or any reintervention. Long term clinical outcome was obtained from an electronic database of hospital records and from questionnaires to the patients and referring physicians. Long term survival status was assessed by written inquiries to the municipal civil registries.
Results: The mean (SD) follow up was 3.6 (1.2) years. The cumulative incidence of MACE at six months was 19.1%, at one year 36.4%, and at four years 58.3%. The target lesion revascularisation (TLR) rate at six months was 12.9%, at one year 28.3%, and at four years 50.4%. From multivariate analysis, dose < 18 Gy was the most significant predictor of TLR. At four years the cumulative incidence of death was 3.8%, of myocardial infarction 13.4%, and of coronary artery bypass surgery 11.3%. Total vessel occlusion was documented in 12.3% of the patients.
Conclusions: In the long term follow up of patients after IRT, there are increased adverse cardiac events beyond the first six months.
Intracoronary β radiation therapy (IRT) has been evaluated as a treatment modality for restenosis prevention. Randomised studies have confirmed its effectiveness for the treatment of in-stent restenosis, both with γ1–3 and with β emitters,4–6 but its effectiveness for de novo lesions especially in combination with the use of stents is questionable.7–9
The safety and effectiveness of IRT in the long term has yet to be determined. In a porcine model of restenosis of balloon and stent arterial injury followed by IRT, the inhibition of neointimal formation observed at one month was not sustained at six months. Furthermore, this lack of effect on neointimal formation was accompanied by subacute and late thrombosis that led to cardiac death.10 Reports on the long term outcome of small randomised studies and registries have raised issues regarding the long term effectiveness of IRT. The angiographic analysis from the SCRIPPS (Scripps coronary radiation to inhibit proliferation post-stenting) trial at three years showed a reduction of the minimum lumen diameter in irradiated patients but not in the placebo group,11 with a further increase in target lesion revascularisation (TLR) between 3–5 years in the irradiated patients only.12 In addition, an increase in the revascularisation rate between six months and three years was observed only in the irradiated group of the gamma-WRIST (Washington radiation for in-stent restenosis trial) randomised trial.13 In both studies the overall clinical benefit of brachytherapy was maintained in the long term.
We report the long term outcome of patients treated with IRT for de novo and in-stent restenotic lesions in our centre.
Between April 1997 and December 2002, 331 patients received IRT in our institution. In four patients irradiation was not successful (total success rate 99%). Fifteen patients treated during 2002 with limited follow up were excluded from this analysis. Another 11 patients who were treated with γ radiation (GRANITE (gamma radiation to atheromatous neointima using intracoronary therapy in Europe) study) were also excluded. In total 301 patients were analysed for determination of the long term follow up after IRT. Table 11 presents the baseline characteristics of the patients. Table 22 presents procedural characteristics and radiation details. The prescribed dose with the strontium-90/yttrium-90 source was based on quantitative coronary angiography (at 2 mm from the centre line of the source axis) and that with the phosphorus-32 source was based on intravascular ultrasound (at a depth of 1 mm at the vessel wall). Figure 11 presents the number of patients treated with IRT each year.
Baseline clinical and procedural data were entered prospectively into a dedicated database. Long term clinical outcome was obtained from an electronic database of hospital records. The Thoraxcentre is a tertiary cardiology centre serving a group of 14 local hospitals and is the only one with facilities for percutaneous interventions in the region of Rotterdam. As required by the local medical system organisation all baseline procedures were performed in this tertiary facility, as well as the vast majority of reinterventions.
Long term survival status was assessed by written inquiries to the municipal civil registries. Questionnaires were sent to all living patients focusing on the occurrence of major adverse cardiac events (MACE) such as myocardial infarction and repeat intervention (surgical and percutaneous). The referring physician and institutions and the general practitioners were directly approached whenever necessary. Complete follow up was obtained for all patients.
Up to six months 168 (56%) patients underwent angiographic control, which was symptomatically driven in almost 25% of these.
MACE were defined as death, non-fatal myocardial infarction, and repeat revascularisation. TLR was defined as any surgical or percutaneous reintervention because of restenosis within the irradiated segment or the 5 mm proximal or distal segment (edge restenosis). Target vessel revascularisation (TVR) was defined as any reintervention driven by lesions located in the treated vessel beyond the target lesion limits. Non-TLR-TVR was defined as any reintervention in vessels other than the target vessel. Coronary artery bypass grafting (CABG) was regarded not as a separate event but as a type of reintervention (TLR, TVR, or non-TLR-TVR). The diagnosis of acute myocardial infarction, indiscriminately Q or non-Q wave, required a rise of creatine kinase to twice the upper limit of normal together with a rise in creatine kinase MB fraction. If myocardial infarction was diagnosed after a patient was admitted to another hospital, the diagnosis was confirmed through direct contact with the referring physician and based on the same criteria.
Total occlusion was defined as occlusion of the irradiated segment documented by coronary angiography. Subacute thrombosis was defined as angiographically documented total occlusion at 30 days. Late total occlusion was defined as angiographically documented total occlusion > 30 days after the intervention. Thrombotic occlusion was defined as an occlusion that resulted in an acute coronary syndrome (myocardial infarction or unstable angina).14
For the determination of the length of follow up, the start day was that of the index procedure with IRT between April 1997 and December 2001. The last day for the follow up was 31 March 2003.
The early period was between April 1997 and June 1999 (at the beginning of routine use of IRT with the RENO registry) and late the period was between July 1999 and December 2001.
Event-free survival was estimated with Kaplan-Meier curves. Among patient subgroups the log rank test was used to compare survival curves. Data are expressed as mean (SD). Continuous variables were compared by Student’s t test and categorical variables by χ2 tests. Significance of all tests was defined at the p < 0.05 level. The independent association of clinical characteristics with long term mortality, infarction, TLR, and vessel occlusion (the first occurrence of death, myocardial infarction, or TLR) was tested by using the Cox proportional hazard model. Preselected preprocedural and periprocedural variables were age, sex, diabetes, hypertension, hypercholesterolaemia, smoking, unstable angina, prior myocardial infarction, prior CABG, extent of coronary artery disease, left ventricular ejection fraction, indication for percutaneous transluminal coronary angioplasty (de novo or in-stent restenosis), device used (stent or balloon), dose (< 18 Gy or Gy), duration of dual antiplatelet medication (< 6 months versus 6 months), source used, and early versus late experience.
The cumulative incidence of MACE at six months was 19.1%, at one year 36.4%, and at four years 58.3%. Figure 22 shows the MACE-free survival curve. Table 33 presents the total MACE count. At four years, the cumulative incidence of MACE was not dependant on the indication (de novo versus in-stent restenosis, p = 0.8), the device used (balloon versus stent, p = 0.5), or the early versus the late experience (p = 0.3). Table 44 presents the independent predictors of MACE.
At four years the cumulative incidence of death was 3.8% and of myocardial infarction 13.4%. Half of the deaths were cardiac in origin. A higher incidence of myocardial infarction was observed in patients treated for de novo lesions than in those treated for in-stent restenosis (13.7% v 6.3%, p = 0.04).
The majority (85%) of reinterventions were TLRs, with low rates of TVR and non-TLR-TVR observed at four years (2.3% and 4.7%, respectively). The cumulative incidence of TLR at six months was 12.9%, at one year 28.3%, and at four years 50.4%. Figure 33 presents the TLR-free survival curve. The mean time to the first TLR was 1.15 (1.0) years. The reintervention-free survival rate at six months was 83.4% and at four years 46.2%. Table 33 presents the total count of TLR and reintervention. At four years, the cumulative incidence of TLR was dependant on neither the indication (de novo versus in-stent restenosis, p = 0.8) nor the device used (balloon versus stent, p = 0.8) (fig 33).). TLR was also independent of the period (early versus late, p = 0.4). The cumulative incidence of TLR was higher in patients who received < 18 Gy than in those who received 18 Gy (p = 0.01) (fig 44).). Table 44 presents the independent predictors of TLR.
A total occlusion was documented in 37 patients (12.3%) (table 33).). The incidence of subacute thrombosis was 0.3% (one of 301) and that of late total occlusion was 12% (36 of 301). Almost half (6.0%) were related to an acute coronary syndrome (late thrombotic occlusion). Six patients underwent TLR before the vessel finally occluded. Patients treated for de novo lesions had a higher incidence of total occlusions than did those treated for in-stent restenosis (15.4% v 7.9%, p = 0.03). The treatment of a de novo lesion was an independent predictor of total vessel occlusion in the long term (hazard ratio 2, 95% confidence interval 1.1 to 5).
In total 30 patients underwent CABG (table 33).). In 15 patients surgery was the first TLR. In 11 patients it was the second TLR, and in one it was the third TLR (recurrence after an initial percutaneous TLR). In two patients CABG was regarded as TVR and in one further patient as non-TLR-TVR.
Very limited data are available for the long term outcome of patients treated with intracoronary radiation for de novo lesions. In the Canadian arm of BERT (beta energy restenosis trial) the TLR rate at six months was 10% and increased to 23% at two years indicating a late catch up phenomenon. The positive remodelling observed at six months was lost due to a decrease in minimum lumen diameter between six months and two years. No death, myocardial infarction, or late vessel occlusion was reported in this small cohort of 30 patients.15
In the WRIST series of patients TLR increased by 14% between six months and two years after both β and γ radiotherapy, significantly higher than the 2% increment in the control group.16 Between two years and three years TLR increased further by 7% in patients treated with γ radiation therapy compared with 2% in the control group13 indicating that radiation therapy may merely delay the restenotic biological process.
The angiographic analysis from the SCRIPPS randomised study showed a reduction of minimum lumen diameter by 0.37 mm between six months and three years in the irradiation group; it remained unchanged in the placebo group.11 Between six months and five years TLR increased by 11.6% (from 11.5% to 23.1%) in the irradiated group compared with only 3.5% (44.8% v 48.3%) in the placebo group; at five years the composite end point of death, myocardial infarction, and TVR no longer reached significance between the two groups.12 In both studies, despite the apparent mitigation of efficacy of radiation over time there remained a significant overall benefit in the clinical outcome of irradiated patients compared with the non-irradiated patients in the long term.
In our population between years 1 and 4, TLR increased from 28% to 50% and MACE from 36% to 58%. These results compare poorly with results after conventional stent implantation. In the BENESTENT (Belgian Netherlands stent) I study TLR at five years was 17.2% (2% increment between years 1 and 5) and total MACE was 34.4% (11% increment between years 1 and 5).17 Even in more complex subsets of patients TLR was not higher than 20% at up to 10 years’ follow up.18,19
There was no difference in the long term outcome based on the indication (de novo versus in-stent restenosis) or the device used (balloon versus stent). Increased dose ( 18 Gy) was the strongest radiation related independent predictor of TLR. In patients treated for de novo lesions in a dose finding study the group who received 18 Gy had a better angiographic outcome than the groups receiving lower doses.7 In the Long WRIST (WRIST for long lesions) study of patients treated for diffuse in-stent restenosis, improved clinical and angiographic outcomes were observed in the group who received 18 Gy compared with placebo and those who received 15 Gy.20 Patients treated with γ radiation in the Venezuela study had a better long term outcome than did patients from SCRIPPS and WRIST, and the authors speculate that this was related to the higher dose administered during this study.21
In the current study the duration of double antiplatelet medication was not a predictor of MACE or TLR. In the WRIST 12 study at 15 months’ follow up, patients who received double antiplatelet medication for 12 months had an improved clinical outcome compared with patients who received medication for only six months.22,23 Since the majority of our patients received double antiplatelet medication for six months or less, the duration was probably not long enough.
The incidences of late total occlusion and late thrombosis after brachytherapy vary between 6–14%.14,24 In our study a 12.3% incidence of occlusion was documented with the majority of events occurring beyond six months. The real incidence was probably underestimated, as we did not consider silent occlusion in asymptomatic patients without angiographic follow up.
Patients treated for de novo lesions had a significantly higher incidence of total occlusions and myocardial infarction suggesting that brachytherapy should not be used for primary prevention of restenosis.
Drug eluting stents have proved to be very effective in preventing restenosis in relatively simple de novo lesions.25 Preliminary reports indicate that this beneficial effect is maintained in the long term (up to two years).26 These results, in combination with the disappointing outcome of brachytherapy for de novo lesions (especially with the use of stents), have had a dramatic impact on the use of brachytherapy in our centre (fig 11).
The broad application of eluting stents may limit brachytherapy as a treatment technique for the limited number of patients with failure of eluting stents.
This is a single centre retrospective analysis with all the limitations originating from such an approach. Patients were enrolled over a period of four and a half years. The dose administered and the duration of dual antiplatelet medication were variable, based on the protocol and the current evidence available at that time.
In the long term follow up of patients after IRT, adverse cardiac events increase beyond the first six months. IRT delays rather than abolishes cardiac events in the long term. Patients treated with IRT require longer follow up evaluation than those treated with standard techniques.
No financial support was received for this study.