Optimum Radiotherapy Schedule for Uterine Cervical Cancer based-on the Detailed Information of Dose Fractionation and Radiotherapy Technique

처방선량 및 치료기법별 치료성적 분석 결과에 기반한 자궁경부암 환자의 최적 방사선치료 스케줄

  • Cho, Jae-Ho (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Kim, Hyun-Chang (Departments of Preventive Medicine and Public Health, Yonsei University Medical School) ;
  • Suh, Chang-Ok (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Lee, Chang-Geol (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Keum, Ki-Chang (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Cho, Nam-Hoon (Departments of Pathology, Yonsei University Medical School) ;
  • Lee, Ik-Jae (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Shim, Su-Jung (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Suh, Yang-Kwon (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Seong, Jinsil (Departments of Radiation Oncology, Yonsei University Medical School) ;
  • Kim, Gwi-Eon (Departments of Radiation Oncology, Yonsei University Medical School)
  • 조재호 (연세대학교 의과대학 방사선종양학교실) ;
  • 김현창 (연세대학교 의과대학 예방의학교실) ;
  • 서창옥 (연세대학교 의과대학 방사선종양학교실) ;
  • 이창걸 (연세대학교 의과대학 방사선종양학교실) ;
  • 금기창 (연세대학교 의과대학 방사선종양학교실) ;
  • 조남훈 (연세대학교 의과대학 병리학교실) ;
  • 이익재 (연세대학교 의과대학 방사선종양학교실) ;
  • 심수정 (연세대학교 의과대학 방사선종양학교실) ;
  • 서양권 (연세대학교 의과대학 방사선종양학교실) ;
  • 성진실 (연세대학교 의과대학 방사선종양학교실) ;
  • 김귀언 (연세대학교 의과대학 방사선종양학교실)
  • Published : 2005.09.01

Abstract

Background: The best dose-fractionation regimen of the definitive radiotherapy for cervix cancer remains to be clearly determined. It seems to be partially attributed to the complexity of the affecting factors and the lack of detailed information on external and intra-cavitary fractionation. To find optimal practice guidelines, our experiences of the combination of external beam radiotherapy (EBRT) and high-dose-rate intracavitary brachytherapy (HDR-ICBT) were reviewed with detailed information of the various treatment parameters obtained from a large cohort of women treated homogeneously at a single institute. Materials and Methods: The subjects were 743 cervical cancer patients (Stage IB 198, IIA 77, IIB 364, IIIA 7, IIIB 89 and IVA 8) treated by radiotherapy alone, between 1990 and 1996. A total external beam radiotherapy (EBRT) dose of $23.4\~59.4$ Gy (Median 45.0) was delivered to the whole pelvis. High-dose-rate intracavitary brachytherapy (HDR-IBT) was also peformed using various fractionation schemes. A Midline block (MLB) was initiated after the delivery of $14.4\~43.2$ Gy (Median 36.0) of EBRT in 495 patients, while In the other 248 patients EBRT could not be used due to slow tumor regression or the huge initial bulk of tumor. The point A, actual bladder & rectal doses were individually assessed in all patients. The biologically effective dose (BED) to the tumor ($\alpha/\beta$=10) and late-responding tissues ($\alpha/\beta$=3) for both EBRT and HDR-ICBT were calculated. The total BED values to point A, the actual bladder and rectal reference points were the summation of the EBRT and HDR-ICBT. In addition to all the details on dose-fractionation, the other factors (i.e. the overall treatment time, physicians preference) that can affect the schedule of the definitive radiotherapy were also thoroughly analyzed. The association between MD-BED $Gy_3$ and the risk of complication was assessed using serial multiple logistic regression models. The associations between R-BED $Gy_3$ and rectal complications and between V-BED $Gy_3$ and bladder complications were assessed using multiple logistic regression models after adjustment for age, stage, tumor size and treatment duration. Serial Coxs proportional hazard regression models were used to estimate the relative risks of recurrence due to MD-BED $Gy_{10}$, and the treatment duration. Results: The overall complication rate for RTOG Grades $1\~4$ toxicities was $33.1\%$. The 5-year actuarial pelvic control rate for ail 743 patients was $83\%$. The midline cumulative BED dose, which is the sum of external midline BED and HDR-ICBT point A BED, ranged from 62.0 to 121.9 $Gy_{10}$ (median 93.0) for tumors and from 93.6 to 187.3 $Gy_3$ (median 137.6) for late responding tissues. The median cumulative values of actual rectal (R-BED $Gy_3$) and bladder Point BED (V-BED $Gy_3$) were 118.7 $Gy_3$ (range $48.8\~265.2$) and 126.1 $Gy_3$ (range: $54.9\~267.5$), respectively. MD-BED $Gy_3$ showed a good correlation with rectal (p=0.003), but not with bladder complications (p=0.095). R-BED $Gy_3$ had a very strong association (p=<0.0001), and was more predictive of rectal complications than A-BED $Gy_3$. B-BED $Gy_3$ also showed significance in the prediction of bladder complications in a trend test (p=0.0298). No statistically significant dose-response relationship for pelvic control was observed. The Sandwich and Continuous techniques, which differ according to when the ICR was inserted during the EBRT and due to the physicians preference, showed no differences in the local control and complication rates; there were also no differences in the 3 vs. 5 Gy fraction size of HDR-ICBT. Conclusion: The main reasons optimal dose-fractionation guidelines are not easily established is due to the absence of a dose-response relationship for tumor control as a result of the high-dose gradient of HDR-ICBT, individual differences In tumor responses to radiation therapy and the complexity of affecting factors. Therefore, in our opinion, there is a necessity for individualized tailored therapy, along with general guidelines, in the definitive radiation treatment for cervix cancer. This study also demonstrated the strong predictive value of actual rectal and bladder reference dosing therefore, vaginal gauze packing might be very Important. To maintain the BED dose to less than the threshold resulting in complication, early midline shielding, the HDR-ICBT total dose and fractional dose reduction should be considered.

목적: 고선량률 강내근접치료와 외부방사선의 병합치료는 자궁경부암의 표준치료법이지만, 최적의 병합 방식 및 선량 분할 스케줄은 아직 정해지지 않고 있다. 부분적으로는 이에 영향을 미치는 인자들의 다양성 및 기존의 문헌들의 방사선 선량에 관한 자세한 정보 부족을 그 이유로 들 수 있다. 이에 본 연구는 고선량률 강내근접치료에 대한 풍부한 경험을 바탕으로 단일기관에서 비교적 균일한 치료를 받은 많은 수의 환자 모집단을 대상으로 이들 다양한 인자들 및 방사선치료에 대한 자세한 분석을 통해서 최적의 방사선치료를 위한 지침을 얻고자 하였다. 대상 및 방법: 1990년부터 1996년까지 연세암센터에서 고선량률 강내근접치료 및 외부방사선치료로 자궁경부암에 대한 근치적 치료를 받은 743명의 환자들을 대상으로 하였으며, 중앙추적관찰 기간은 52개월이었다. FIGO 병기 분포는 IB 198명, IIA 77명, IIB 364명, IIIA 7명, IIIB 89명, IVA 8명이었다. 전골반방사선 선량은 $23.4\~59.4$ Gy (중앙값 45 Gy)의 분포를 보였으며, 진단 시 종양의 크기 및 외부방사선치료에 대한 종양의 반응에 따라서 그 시기를 조절하는 중앙차폐는 495예에서 시행되었으며, 그 시기는 $14.4\~43.2$ Gy (중앙값 36.0 Gy)로 비교적 광범위하고 다양한 분포를 보였다. 강내근접치료와 외부방사선치료의 분할 선량 차이를 극복하기 위해 생물학적 유효선량(Biologically Effective Dose, BED) 개념을 적용하였으며, 종양 및 정상 조직에 대한 $\alpha/\beta$비는 각각 10 및 3으로 하였다. 모든 개별 환자의 직장 전벽 및 방광 흡수선량을 분석하였고, 합병증 및 골반제어율과의 상관 관계를 규명하고자 하였다. 이외에도 방사선치료 스케줄에 영향을 미칠 수 있는 인자들인 총 치료기간, 강내근접치료의 분할 선량 크기, 주치의의 선호도에 따른 치료 스케줄 차이 등도 함께 고려하여 분석하였다. 결과: 전체 환자에서 RTOG Grade 1-4독성 발생률은 $33.1\%$였다. 전체 환자의 5년 골반제어율은 $83\%$로 분석되었다. 중앙차폐이전 외부방사선선량과 강내근접치료의 합산 BED값(=MD-BED $Gy_{\alpha/\beta}$$\alpha/\beta$=10인 경우 $62.0\~121.9\;Gy_{10}$ (중앙값: $93.0\;Gy_{10}$)의 분포를, ${\alpha/\beta}=3$인 경우 $93.6\~187.3\;Gy_3$ (중앙값=$137.6\;Gy_3$ )의 분포를 보였다. MD-BED $Gy_3$는 직장합병증 발생과의 관계는 통계적으로 유의하였고, 방광합병증과는 유의하지 않았다. 직장합병증과의 연관성은 MD-BED $Gy_3$보다 개별 환자의 직장전벽 총 선량 BED값인 R-BED $Gy_3$가 훨씬 더 높았다. 요도카테터 풍선의 후방지점이 대변하는 방광의 총 선량 BED값인 V-BED $Gy_3$도 방광합병증과 경향성 테스트에서 통계적 유의성을 보였다. 하지만, 어떠한 방사선선량도 골반제어율과 의미 있는 상관관계를 보이지 않았다. 본 기관에서 주치의의 선호도에 따라 강내근접치료가 외부방사선치료의 중간에 시행되는 형태인 샌드위치기법과 외부방사선치료 후반부에 시행되는 순차적 기법으로 구분하였을 때, 두 방식간 치료성적 및 합병증의 차이는 없었다. 총 치료기간에 대한 분석에서는 치료기간이 길어질수록 재발 위험이 커지는 경향을 보였으나, 나이 및 병기, 종양의 크기, MD-BED $Gy_{10}$ 등의 예후 인자를 보정한 다변량분석에서는 치료기간이 100일 이상인 경우에만 통계적으로 유의하게 증가하였다. 강내근접치료 분할선량 크기인 3 Gy와 5 Gy 사이에 골반제어율 및 합병증의 차이는 없었다. 결론: 자궁경부암의 최적방사선치료 스케줄에 대한 지침을 세우기 어렵게 만드는 가장 중요한 이유는 강내근접치료가 갖는 선량분포 특성에서 기인하는 방사선선량-골반제어율 상관 관계의 부재 및 개별 종양의 방사선에 대한 반응 속도가 환자마다 크게 다를 수 있다는 점이다. 따라서 전체적인 원칙과 함께 개인화된 맞춤치료가 필요하다. 치료 지침에 영향을 미칠 수 있는 요소들의 복합적인 고려도 중요하다고 할 수 있겠다. 합병증 발생이 우려되는 경우 생물학적 유효선량을 낮추기 위해 적절한 조기 중앙차폐 및 강내근접치료의 분할선량 크기 감소를 고려해볼 수 있다.

Keywords

References

  1. Henschke UK, Hilaris BS, Mahan GD. Remote afterloading with intracavitary applicators. Radiology 1964;83:344-345 https://doi.org/10.1148/83.2.344
  2. O'Connell D, Howard N, Joslin CAF, Ramsey NW, Liversage WE. A new remotely controlled unit for the treatment of uterine carcinoma. Lancet 1965;18:570-571
  3. Shigematsu Y, Nishiyama K, Masaki N, et al. Treatment of carcinoma of the uterine cervix by remotely afterloading intracavitary radiotherapy with high dose rate: a comparative study with a low-dose system. Int J Radiat Oncol Biol Phys 1983;9:351-356 https://doi.org/10.1016/0360-3016(83)90295-X
  4. Teshima T, Inoue T, Ikeda H, et al. High-dose rate and low-dose rate intracavitary therapy for carcinoma of the uterine cervix. Cancer 1993;72:2409-2414 https://doi.org/10.1002/1097-0142(19931015)72:8<2409::AID-CNCR2820720819>3.0.CO;2-N
  5. Patel FD, Sharma SC, Negi PS, et al. Low dose rate vs. high dose rate brachytherapy in the treatment of carcinoma of the uterine cervix: a clinical trial. Int J Radiat Oncol Biol Phys 1994;28:335-341 https://doi.org/10.1016/0360-3016(94)90055-8
  6. Fu KK, Phillips TL. High-dose-rate versus low-dose-rate intracavitary brachytherapy for carcinoma of the cervix. Int J Radiat Oncol Biol Phys 1990;19:791-796 https://doi.org/10.1016/0360-3016(90)90511-H
  7. Orton GO. High and low dose-rate brachytherapy for cervicalcarcinoma. Acta Oncol 1998;37;117-125 https://doi.org/10.1080/028418698429667
  8. Petreit DG, Pearcey R. Literature analysis of high dose rate brachytherapy fractionation scheduled in the treatment of cervical cancer : is there an optimal fractionation schedule? Int J Radiat Oncol Biol Phys 1999;43:359-366 https://doi.org/10.1016/S0360-3016(98)00387-3
  9. Nag S, Erickson B, Thomadsen B, Orton C, Demanes JD, Petereit D. The American Brachytherapy Society recommendations for high-dose-rate brachytherapy for carcinoma of the cervix. Int J Radiat Oncol Biol Phys 2000;48:201-211 https://doi.org/10.1016/S0360-3016(00)00497-1
  10. Perez CA, Grigsby PW, Castro-Vita H, Lockett MA. Carcinoma of the uterine cervix. I. Impact of prolongation of overall treatment time and timing of brachytherapy on outcome of radiation therapy. Int J Radiat Oncol Biol Phys 1995;32: 1275-1288 https://doi.org/10.1016/0360-3016(95)00220-S
  11. Petereit DG, Sarkaria JN, Chappell R, et al. The adverse effect of treatment prolongation in cervical carcinoma. Int J Radiat Oncol Biol Phys 1995;32:1301-1307 https://doi.org/10.1016/0360-3016(94)00635-X
  12. Lanciano RM, Pajak TF, Martz K, Hanks GE. The influence of treatment time on outcome for squamous cell cancer of the uterine cervix treated with radiation: a patternsof- care study. Int J Radiat Oncol Biol Phys 1993;25:391-397 https://doi.org/10.1016/0360-3016(93)90058-4
  13. Park HC, Suh CO, Kim GE. Fractionated high-dose-rate brachytherapy in the management of uterine cervical cancer. Yonsei Med J 2002;43:737-748 https://doi.org/10.3349/ymj.2002.43.6.737
  14. Suh CO, Kim GE, Loh JJK. Treatment of carcinoma of the uterine cervix with high-dose-rate intracavitary irradiation using Ralstron. J Korean Soc Ther Radiol Oncol 1990;8:231-239
  15. Kim GE, Suh CO, Lee DH, Park CY. Treatment for uterine cervical cancer using high-dose-rate Co-60 sources. J Korean Soc Ther Radiol Oncol 1983;1:95-102
  16. Kim WC, Kim GE, Suh CO, Loh JJK. High versus low dose rate intracavitary irradiation for adenocarinoma of the uterine cervix. Jpn J Clin Oncol 2001;31:432-437 https://doi.org/10.1093/jjco/hye098
  17. Chung EJ, Kim GE, Suh CO, Keum KC, Kim WC. Late rectal complication in patients with high dose rate brachytherapy for stage IIB carcinoma of the cervix. J Korean Soc Ther Radiol Oncol 1996;14:41-52
  18. Lee SW, Suh CO, Chung EJ, et al. Optimum dose combination of external radiation and high dose rate ICR in FIGO IB uterine cervical cancer. J Korean Soc Ther Radiol Oncol 1996;14:201-209
  19. Fowler JF. The linear-quadratic formula and progress in fractionated radiotherapy. Br J Radiol 1989;62:679-694 https://doi.org/10.1259/0007-1285-62-740-679
  20. Toita T, Kakinohana Y, Ogawa K, et al. Combination external beam radiotherapy and high-dose-rate intracavitary brachytherapy for uterine cervical cancer: analysis of dose and fractionation schedule. Int J Radiat Oncol Biol Phys 2003;56: 1344-1353 https://doi.org/10.1016/S0360-3016(03)00288-8
  21. Ogino I, Kitamura T, Okamoto N, et al. Late rectal complication following high dose rate intracavitary brachytherapy in cancer of the cervix. Int J Radiat Oncol Biol Phys 1995;31:725-734 https://doi.org/10.1016/0360-3016(94)00547-8
  22. Clark BG, Souhami L, Roman TN, Chappell R, Evans MD, Fowler JF. The prediction of late rectal complications in patients treated with high dose-rate brachytherapy for carcinoma of the cervix. Int J Radiat Oncol Biol Phys 1997;38: 989-993 https://doi.org/10.1016/S0360-3016(97)00074-6
  23. Ferrigno R, dos Santos Novaes PE, Pellizzon AC, et al. High-dose-rate brachytherapy in the treatment of uterine cervix cancer. Analysis of dose effectiveness and late complications. Int J Radiat Oncol Biol Phys 2001;50:1123-1135 https://doi.org/10.1016/S0360-3016(01)01533-4
  24. Chen SW, Liang JA, Yeh LS, Yang SN, Shiau AC, Lin FJ. Comparative study of reference points by dosimetric analyses for late complications after uniform external radiotherapy and high-dose-rate brachytherapy for cervical cancer. Int J Radiat Oncol Biol Phys 2004;60:663-671 https://doi.org/10.1016/j.ijrobp.2004.05.028