MSOR04 Presentation Time: 8:45 AM: Outcomes with High Dose Rate Brachytherapy in Reirradiation of Head and Neck Cancers
Brachytherapy(2023)
摘要
Purpose Reirradiation of recurrent or second primary head and neck cancers (HNC) after prior therapy is a challenge. After prior definitive external beam radiotherapy (EBRT), reirradiation is limited by normal tissue tolerances and expected outcomes are modest with a minority achieving durable control. Outcomes of EBRT reirradiation have been widely variable, historically reporting 2-year locoregional control (LRC) rates of 40-60% and overall survival (OS) rates of 15-30%, with a small number of series achieving LRC rates up to ∼60%. Reirradiation can be associated with increased morbidity with high grade toxicity rates estimated at ∼25-50%. This study evaluated the hypothesis that high dose rate brachytherapy (HDR-BT) would improve cancer outcomes without worse toxicity. Materials and Methods Included were all patients treated with HDR-BT after having previously received definitive EBRT for primary HNC squamous cell carcinoma (SCC) from 2011-2021. Patients had either recurrent disease or second HNC primaries. Clinical and treatment characteristics and CTCAE-graded toxicity were summarized with descriptive statistics. Survival outcomes were estimated with the Kaplan Meier method. Results Twenty-three patients were evaluated. Median follow up time was 19mo (IQR 12-36mo). Median age at time of HDR-BT was 64 years (IQR 60-69 years). Thirteen patients (57%) were treated for recurrent HNC, of which 7 were in the oral cavity and 6 were in the oropharynx. Ten patients (43%) were treated for a second primary HNC, of which 5 were in the oral cavity and 5 were in the oropharynx. Median time from completion of prior EBRT to receiving HDR-BT was 41mo (IQR 14-73mo). Within their retreatment course, 11 patients (48%) were treated with HDR-BT after resection, 9 patients (39%) received concurrent hyperthermia, and 7 patients (30%) received chemotherapy. HDR-BT regimens included 600cGy x5 (N=11), 600cGy x6 (N=6), 450cGy x8 (N=1), 1500cGy x1 (N=1),1000cGy x1 (N=1), 500cGy x8 (N=1), and 700cGy x5 (N=1). One patient who was treated with two implants received 450cGy x 3 followed by 475cGy x5. Nine patients (39%) experienced grade ≥3 toxicity. These toxicities consisted of fistula, soft tissue necrosis, osteoradionecrosis, ulcer, hemorrhage, and dysphagia requiring a chronic feeding tube. Nine patients (39%) experienced a local recurrence with a median local control of 29mo. Three patients (13%) experienced regional relapse, and median regional control was not reached. Ten patients (43%) remained alive at the time of analysis, and median overall survival time was 17mo. Actuarial 2-year local control, regional control, and OS rates were 68%, 89%, and 62%, respectively. Conclusion Our data suggests that HDR-BT for re-irradiation of HNC can provide durable control compared to historical reports and should be further explored as a salvage treatment option for recurrent or second primary HNC. In addition, potential associated toxicities of HDR-BT do not apparently occur at a higher rate than expected with standard reirradiation. Reirradiation of recurrent or second primary head and neck cancers (HNC) after prior therapy is a challenge. After prior definitive external beam radiotherapy (EBRT), reirradiation is limited by normal tissue tolerances and expected outcomes are modest with a minority achieving durable control. Outcomes of EBRT reirradiation have been widely variable, historically reporting 2-year locoregional control (LRC) rates of 40-60% and overall survival (OS) rates of 15-30%, with a small number of series achieving LRC rates up to ∼60%. Reirradiation can be associated with increased morbidity with high grade toxicity rates estimated at ∼25-50%. This study evaluated the hypothesis that high dose rate brachytherapy (HDR-BT) would improve cancer outcomes without worse toxicity. Included were all patients treated with HDR-BT after having previously received definitive EBRT for primary HNC squamous cell carcinoma (SCC) from 2011-2021. Patients had either recurrent disease or second HNC primaries. Clinical and treatment characteristics and CTCAE-graded toxicity were summarized with descriptive statistics. Survival outcomes were estimated with the Kaplan Meier method. Twenty-three patients were evaluated. Median follow up time was 19mo (IQR 12-36mo). Median age at time of HDR-BT was 64 years (IQR 60-69 years). Thirteen patients (57%) were treated for recurrent HNC, of which 7 were in the oral cavity and 6 were in the oropharynx. Ten patients (43%) were treated for a second primary HNC, of which 5 were in the oral cavity and 5 were in the oropharynx. Median time from completion of prior EBRT to receiving HDR-BT was 41mo (IQR 14-73mo). Within their retreatment course, 11 patients (48%) were treated with HDR-BT after resection, 9 patients (39%) received concurrent hyperthermia, and 7 patients (30%) received chemotherapy. HDR-BT regimens included 600cGy x5 (N=11), 600cGy x6 (N=6), 450cGy x8 (N=1), 1500cGy x1 (N=1),1000cGy x1 (N=1), 500cGy x8 (N=1), and 700cGy x5 (N=1). One patient who was treated with two implants received 450cGy x 3 followed by 475cGy x5. Nine patients (39%) experienced grade ≥3 toxicity. These toxicities consisted of fistula, soft tissue necrosis, osteoradionecrosis, ulcer, hemorrhage, and dysphagia requiring a chronic feeding tube. Nine patients (39%) experienced a local recurrence with a median local control of 29mo. Three patients (13%) experienced regional relapse, and median regional control was not reached. Ten patients (43%) remained alive at the time of analysis, and median overall survival time was 17mo. Actuarial 2-year local control, regional control, and OS rates were 68%, 89%, and 62%, respectively. Our data suggests that HDR-BT for re-irradiation of HNC can provide durable control compared to historical reports and should be further explored as a salvage treatment option for recurrent or second primary HNC. In addition, potential associated toxicities of HDR-BT do not apparently occur at a higher rate than expected with standard reirradiation.
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