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  • [J Clin Oncol] Ablative Radiotherapy Doses Lead to a Substantial Prolongation of Survival in Patients With Inoperable Intrahepatic Cholangiocarcinoma: A Retrospective Dose Response Analysis.

    The University of Texas MD Anderson Cancer Center / Randa Tao, Christopher H. Crane*

  • 출처
    J Clin Oncol.
  • 등재일
    2016 Jan 20
  • 저널이슈번호
    34(3):219-26. doi: 10.1200/JCO.2015.61.3778. Epub 2015 Oct 26.
  • 내용

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    Abstract
    PURPOSE:
    Standard therapies for localized inoperable intrahepatic cholangiocarcinoma (IHCC) are ineffective. Advances in radiotherapy (RT) techniques and image guidance have enabled ablative doses to be delivered to large liver tumors. This study evaluated the effects of RT dose escalation in the treatment of IHCC.

    PATIENTS AND METHODS:
    Seventy-nine consecutive patients with inoperable IHCC were identified and treated with definitive RT from 2002 to 2014. At diagnosis, the median tumor size was 7.9 cm (range, 2.2 to 17 cm). Seventy patients (89%) received systemic chemotherapy before RT. RT doses were 35 to 100 Gy (median, 58.05 Gy) in three to 30 fractions for a median biologic equivalent dose (BED) of 80.5 Gy (range, 43.75 to 180 Gy).

    RESULTS:
    Median follow-up time for patients alive at time of analysis was 33 months (range, 11 to 93 months). Median overall survival (OS) time after diagnosis was 30 months; 3-year OS rate was 44%. Radiation dose was the single most important prognostic factor; higher doses correlated with an improved local control (LC) rate and OS. The 3-year OS rate for patients receiving BED greater than 80.5 Gy was 73% versus 38% for those receiving lower doses (P = .017); 3-year LC rate was significantly higher (78%) after a BED greater than 80.5 Gy than after lower doses (45%, P = .04). BED as a continuous variable significantly affected LC (P = .009) and OS (P = .004). There were no significant treatment-related toxicities.

    CONCLUSION:

    Delivery of higher doses of RT improves LC and OS in inoperable IHCC. A BED greater than 80.5 Gy seems to be an ablative dose of RT for large IHCCs, with long-term survival rates that compare favorably with resection.

     

     

    Author information

    Tao R1, Krishnan S1, Bhosale PR1, Javle MM1, Aloia TA1, Shroff RT1, Kaseb AO1, Bishop AJ1, Swanick CW1, Koay EJ1, Thames HD1, Hong TS1, Das P1, Crane CH2.
    1Randa Tao, Sunil Krishnan, Priya R. Bhosale, Milind M. Javle, Thomas A. Aloia, Rachna T. Shroff, Ahmed O. Kaseb, Andrew J. Bishop, Cameron W. Swanick, Eugene J. Koay, Howard D. Thames, Prajnan Das, and Christopher H. Crane, The University of Texas MD Anderson Cancer Center, Houston, TX; and Theodore S. Hong, Harvard Medical School, Boston, MA.

    2Randa Tao, Sunil Krishnan, Priya R. Bhosale, Milind M. Javle, Thomas A. Aloia, Rachna T. Shroff, Ahmed O. Kaseb, Andrew J. Bishop, Cameron W. Swanick, Eugene J. Koay, Howard D. Thames, Prajnan Das, and Christopher H. Crane, The University of Texas MD Anderson Cancer Center, Houston, TX; and Theodore S. Hong, Harvard Medical School, Boston, MA. ccrane@mdanderson.org. 

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