Long duration mild temperature hyperthermia and brachytherapy

References

• Ben-Hur E, Bronk By, Elkind MM. Thermally enhanced radiosensitivity of cultured Chinese hamster cells. Nat New Biol 1972; 238: 209–11.
   Google Scholar
• Ben-Hur E, Elkind MM, Bronk By. Thermally enhanced radioresponse of cultured Chinese hamster cells: inhibition of repair of sublethal damage and enhancement of lethal damage. Radiat Res 1974; 58: 38–51.
   Google Scholar
• Harisiadis L, Sung DI, Kessaris N, Hall EJ. Hyperthermia and low dose rate irradiation. Radiology 1978; 129: 195–8.
   PubMed Web of Science ®Google Scholar
• Gerner EW, Oval JR, Manning MR, Sim DA, Bowden GT, Hevezi JM. Dose rate dependence of heat radiosensitization. Int J Radiat Oncol Biol Phys 1983; 9: 1401–4.
   PubMed Web of Science ®Google Scholar
• Ling CC, Robinson E. Moderate hyperthermia and low dose rate irradiation. Radiat Res 1988; 114: 379–84.
   PubMed Web of Science ®Google Scholar
• Corry PM, Martinez A, Armour EP, Edmundson G. Simultaneous hyperthermia and brachytherapy with remote afterloading. In: Martinez A, Orton C, Mould R, eds, Brachytherapy HDR and LDR. Proceedings of the Brachytherapy Meeting Remote Afterloading: State of the Art, 4–6 May 1989, Dearborn: Nucletron, 1990.
   Google Scholar
• Corry P, Armour EP, Gersten D, Martinez A. Hyperthermia and brachytherapy. In: Joslin CAE, Flynn A, Hall EJ. eds, Principles and Practice of Brachytherapy, London: Arnold Publishing. 2001: 400–9.
   Google Scholar
• Armour EP, Wang ZH, Corry PM, Martinez A. Sensitization of rat 9L gliosarcoma cells to low dose rate irradiation by long duration 41 degrees C hyperthermia. Cancer Res 1991; 51: 3088–95.
   PubMed Web of Science ®Google Scholar
• Wang Z, Armour EP, Corry PM, Martinez A. Elimination of dose rate effects by mild hyperthermia. Int j Radiat Oncol Biol Phys 1992; 24: 965–73.
   PubMed Web of Science ®Google Scholar
• Spiro Ii, McPherson S, Cook JA, Ling CC, DeGraff W, Mitchell JB. Sensitization of low-dose rate irradiation by nonlethal hyperthermia. Radiat Res 1991; 127: 111–14.
   PubMed Web of Science ®Google Scholar
• Hahn GM, Ning SC, Elizaga M, Kapp DS, Anderson RL. A comparison of thermal responses of human and rodent cells. Int j Radiat Biol 1989; 56: 817–25.
   Google Scholar
• Roizin-Towle L, Pirro JP, McDowell J. A comparison of the heat and radiation sensitivity of rodent and human derived cells cultured in vitro. Int J Radiat Oncol Biol Phys 1986; 12: 647–53.
   Google Scholar
• Mackey MA, Anolik SL, Roti Roti JL. Changes in heat and radiation sensitivity during long duration, moderate hyperthermia in HeLa S3 cells. Int j Radiat Oncol Biol Phys 1992; 24: 543–50.
   Google Scholar
• Armour EP, McEachern D, Wang Z, Corry PM, Martinez A. Sensitivity of human cells to mild hyperthermia. Cancer Res 1993; 53: 2740–4.
   Google Scholar
• Raaphorst GP, Mao J, Ng CE. Thermotolerance in human glioma cells. Int J Hyperthermia 1995; 11: 523–9.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Mao JP, Yang DP, Ng CE. Comparison of thermotolerance development in three human cell lines. Endocurietherapyl Hypertherrnia Oncology 1996; 12: 231–40.
   Google Scholar
• Raaphorst GP, Heller DP, Bussey A, Ng CE. Thermal radiosensitization by 41 degrees C hyperthermia during low dose rate irradiation in human normal and tumour cell lines. Int J Hyperthermia 1994; 10: 263–70.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Bussey A, Heller DP, Ng CE. Comparison of thermoradiosensitization in two human melanoma cell lines and one fibroblast cell line by concurrent mild hyperthermia and low-dose rate irradiation. Radiat Res 1994; 137: 338–45.
   PubMed Web of Science ®Google Scholar
• Wigle JC, Sutherland RM. Increased thermoresistance developed during growth of small multicellular spheroids. J Cell Physiol 1985; 122: 281–9.
   PubMed Web of Science ®Google Scholar
• Armour EP, Gersten D, Martinez A, Corry PM. Enhancement of brachytherapy by long duration-mild temperature hyperthermia. In: Hagen DH, Jung H, Streffer C, eds, Radiation Research 1895–1995 Congress Proceedings, Wurzburg: Universitatsdruckerei H. Sturtz AG, 1996: 1001–4.
   Google Scholar
• Armour E, Wang ZH, Corry P, Martinez A. Equivalence of continuous and pulse simulated low dose rate irradiation in 9L gliosarcoma cells at 37 degrees and 41 degrees C. Int J Radiat Oncol Biol Phys 1992; 22: 109–14.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Ng CE, Shahine B. Comparison of radiosensitization by 41 degrees C hyperthermia during low dose rate irradiation and during pulsed simulated low dose rate irradiation in human glioma cells. Int J Radiat Oncol Biol Phys 1999; 44: 185–8.
   Google Scholar
• Armour EP, Wang Z, Corry PM, Chen PY, Martinez A. Hyperthermic enhancement of high dose rate irradiation in 9L gliosarcoma cells. Int J Radiat Oncol Biol Phys 1994; 28: 171–7.
   PubMed Web of Science ®Google Scholar
• Emami B, Perez CA, Leybovich L, Straube W, Vongerichten D. Interstitial thermora-diotherapy in treatment of malignant tumours. Int J Hypertherrnia 1987; 3: 107–18.
   Google Scholar
• Kapp KS, Kapp DS, Stuecklschweiger G, Berger A, Geyer E. Interstitial hyperthermia and high dose rate brachytherapy in the treatment of anal cancer: a phase I/II study. Int J Radiat Oncol Biol Phys 1994; 28: 189–99.
   Google Scholar
• Mack CF, Stea B, Kittelson JM, Shimm DS, Sneed PK, Phillips TL, Swift PS, Luk Stauffer PR, Chan KW, Steeves Cassady JR, Cetas T. Interstitial thermoradiotherapy with ferromagnetic implants for locally advanced and recurrent neoplasms. Int J Radiat Oncol Biol Phys 1993; 27: 109–15.
   Google Scholar
• Seegenschmiedt MR, Sauer R, Miyamoto C, Chalal JA, Brady LW. Clinical experience with interstitial thermoradiotherapy for localized implantable pelvic tumors. Am J Clin Oncol 1993; 16: 210–22.
   Google Scholar
• Sneed PK, Gutin PH, Stauffer PR, Phillips TL, Prados MD, Weaver KA, Suen S, Lamb Ham B, Ahn D, Lamborn K, Larson DA, Wara WM. Thermoradiotherapy of recurrent malignant brain tumors. Int J Radiat Oncol Biol Phys 1992; 23: 853–61.
   PubMed Web of Science ®Google Scholar
• Corry PM, Robinson S, Getz S. Hyperthermic effects on DNA repair mechanisms. Radiology 1977; 123: 475–82.
   Google Scholar
• Jorritsma JB, Konings AW. Inhibition of repair of radiation-induced strand breaks by hyperthermia, and its relationship to cell survival after hyperthermia alone. Int J Radiat Biol Relat Stud Phys Chem Med 1983; 43: 505–16.
   PubMed Web of Science ®Google Scholar
• Dewey WC. Mechanism of thermal radiosensitization. In: Urano M, Douple E, eds. Hypertherrnia and Oncology, Utretcht: VSP, 1989: 1–15.
   Google Scholar
• Raaphorst GP. Thermal radiosensitization in vitro. In: Urano M, Douple E, eds. Hypertherrnia and Oncology, Utretcht: VSP, 1989: 17–51.
   Google Scholar
• Mills MD, Meyn RE. Hyperthermic potentiation of unrejoined DNA strand breaks following irradiation. Radiat Res 1983; 95: 327–38.
   PubMed Web of Science ®Google Scholar
• Dikomey E. Effect of hyperthermia at 42 and 45 degrees C on repair of radiation-induced DNA strand breaks in CHO cells. Int J Radiat Biol Relat Stud Phys Chem Med 1982; 41: 603–14.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Yang DP, Ng CE. Comparison of survival and DNA double strand breaks for mild hyperthermia and low dose rate/pulsed low dose rate irradiation in human cells. J Therm Biol 2000; 25: 305–11.
   Google Scholar
• Raaphorst GP, Feeley MM. Hyperthermia radiosensitization in human glioma cells comparison of recovery of polymerase activity, survival, and potentially lethal damage repair. Int J Radiat Oncol Biol Phys 1994; 29: 133–9.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Feeley MM, Chu GL, Dewey WC. A comparison of the enhancement of radiation sensitivity and DNA polymerase inactivation by hyperthermia in human glioma cells. Radiat Res 1993; 134: 331–6.
   PubMed Web of Science ®Google Scholar
• Spiro IJ, Denman DL, Dewey WC. Effect of hyperthermia on CHO DNA polymerases alpha and beta. Radiat Res 1982; 89: 134–49.
   PubMed Web of Science ®Google Scholar
• Dikomey E, Jung H. Correlation between polymerase Beta activity and thermal radio-sensitization in Chinese hamster ovary cells. Recent results. Cancer Res 1988; 109: 335–41.
   Google Scholar
• Raaphorst GP, Yang DP, Bussey A, Ng CE. Cell killing, DNA polymerase inactivation and radiosensitization to low dose rate irradiation by mild hyperthermia in four human cell lines. Int J Hypertherrnia 1995; 11: 841–54.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Yang DP, Niedbala G. Is DNA polymerase beta important in thermal radiosensitization? Int J Hypertherrnia 2003 (this issue).
   Google Scholar
• Woudstra EC, Konings AW, Jeggo PA, Kampinga HR. Role of DNA-PK subunits in radiosensitization by hyperthermia. Radiat Res 1999; 152: 214–18.
   PubMed Web of Science ®Google Scholar
• Rauth AM, Melo T, Misra V. Bioreductive therapies: an overview of drugs and their mechanisms of action. Int J Radiat Oncol Biol Phys 1998; 42: 755–62.
   Google Scholar
• Adams GE. The clinical relevance of tumour hypoxia. Eur J Cancer 1990; 26: 420–1.
   PubMed Web of Science ®Google Scholar
• Gerweck LE, Nygaard TG, Burlett M. Response of cells to hyperthermia under acute and chronic hypoxic conditions. Cancer Res 1979; 39: 966–72.
   Google Scholar
• Durand RE. Effects of hyperthermia on the cycling, noncycling, and hypoxic cells of irradiated and unirradiated multicell spheroids. Radiat Res 1978; 75: 373–84.
   PubMed Web of Science ®Google Scholar
• Gerweck LE, Gillette EL, Dewey WC. Killing of Chinese hamster cells in vitro by heating under hypoxic or aerobic conditions. Eur J Cancer 1974; 10: 691–3.
   Google Scholar
• Overgaard J, Bichel P. The influence of hypoxia and acidity on the hyperthermic response of malignant cells in vitro. Radiology 1977; 123: 511–14.
   PubMed Web of Science ®Google Scholar
• Kim JR, Kim SH, Hahn EW. Hypoxic cell radiosensitization by moderate hyperthermia and glucose deprivation. Radiat Res 1983; 93: 416–20.
   Google Scholar
• Mivechi NF, Hofer KG, Hofer MG. Influence of hypoxia and acidity on thermal radio-sensitization and direct heat-induced death of BP-8 sarcoma cells. Radiology 1981; 138: 465–71.
   Google Scholar
• Power JA, Harris JW. Response of extremely hypoxic cells to hyperthermia: survival and oxygen enhancement ratios. Radiology 1977; 123: 767–70.
   PubMed Web of Science ®Google Scholar
• Eddy HA. Alterations in tumor microvasculature during hyperthermia. Radiology 1980; 137: 515–21.
   PubMed Web of Science ®Google Scholar
• Scheid P. Funktionale Besunderheiten der Mikrozirkulation im Kazionom. Bibliotheca Anatornica 1961; 1: 327–35.
   Google Scholar
• Song CW, Kang MS, Rhee JG, Levitt SH. Effect of hyperthermia on vascular function in normal and neoplastic tissues. Ann NY Acad Sci 1980; 335: 35–47.
   PubMedGoogle Scholar
• Song CW. Role of blood flow in hyperthermia. In: Urano M, Douple E, eds, Hypertherrnia and Oncology, Utrecht: VSP, 1991: 275–315.
   Google Scholar
• Shakil A, Osborn JL, Song CW. Changes in oxygenation status and blood flow in a rat tumor model by mild temperature hyperthermia. Int J Radiat Oncol Biol Phys 1999; 43: 859–65.
   Google Scholar
• Song CW, Park H, Griffin RI Improvement of tumor oxygenation by mild hyperthermia. Radiat Res 2001; 155: 515–28.
   PubMed Web of Science ®Google Scholar
• Vujaskovic Z, Poulson JM, Gaskin AA, Thrall DE, Page RL, Charles HC, MacFall JR, Brizel DM, Meyer RE, Prescott DM, Samulski TV, Dewhirst MW. Temperature-depen-dent changes in physiologic parameters of spontaneous canine soft tissue sarcomas after combined radiotherapy and hyperthermia treatment. Int j Radiat Oncol Biol Phys 2000; 46: 179–85.
   PubMed Web of Science ®Google Scholar
• Waterman FM, Nerlinger RE, Moylan Did, Leeper DB. Response of human tumor blood flow to local hyperthermia. Int J Radiat Oncol Biol Phys 1987; 13: 75–82.
   PubMed Web of Science ®Google Scholar
• Niedbala M, Ng CE, Raaphorst GP. Response to pulsed dose rate irradiation with and without mild hyperthermia using tumour and normal cell lines. Int J Hypertherrnia 2001; 17: 536–44.
   Google Scholar
• Dewey WC, Holahan PK. Thermotolerance as a modifier of radiation toxicity. In: Henle KJ, ed., Thermotolerance, Boca Raton: CRC Press, 1987: 113–25.
   Google Scholar
• Henle KJ, Dethlefsen LA. Heat fractionation and thermotolerance: a review. Cancer Res 1978; 38: 1843–51.
   PubMed Web of Science ®Google Scholar
• Henle KJ. Thermotolerance in cultured mammalian cells. In: Henle KJ, ed., Thermotolerance, Boca Raton: CRC Press, 1987: 13–71.
   Google Scholar
• Henle KJ, Nagle WA, Moss Ai. Effect of thermotolerance on the cellular heat-radiation response. In: Urano M, Douple E, eds, Hypertherrnia and Oncology, Zeist, The Netherlands: USP Publishers, 1989: 53–81.
   Google Scholar
• Mackey MA. In vitro effects and biological potential of long duration, moderate hyperthermia. In: Seegenschmiedt MH, Sauer R, eds, Medical Radiology Interstitial and Intracavitary Therrnoradiotherapy, Berlin: Springer, 1993.
   Google Scholar
• Raaphorst GP, Azzam El. Thermal radiosensitization in Chinese hamster (V79) and mouse C3H 10T1/2 cells. The thermotolerance effect. Br J Cancer 1983; 48: 45–54.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Mao JP, Ng CE. Thermotolerance effects on thermoradiosensitization in human glioma cells. Int j Hypertherrnia 1998; 14: 85–95.
   PubMed Web of Science ®Google Scholar
• Heller DP, Raaphorst GP. Low dose rate irradiation of human glioma cells and thermoradiosensitization by mild hyperthermia. Radiation Oncology Investigations 1993; 1: 218–26.
   Google Scholar
• Armour E, Wang Z, Corry P, Martinez A. Thermotolerance and radiation sensitizing effects of long duration, mild temperature hyperthermia. Int J Hyperthermia 1994; 10: 315–24.
   PubMed Web of Science ®Google Scholar
• Urano M, Douple E, eds, Thermal Effects on Cells and Tissues, Utrecht: VSP, 1988.
   Google Scholar
• Urano M, Douple E, eds, Biology of Thermal Potentiation of Radiotherapy, Utrecht: VSP, 1989.
   Google Scholar
• Urano M, Douple E, eds, Interstitial Hyperthermia: Physics, Biology and Clinical Aspects, Utrecht: VSP, 1992.
   Google Scholar
• Urano M, Douple E, eds, Cherno Potentiation by Hyperthermia, Utrecht: VSP, 1994.
   Google Scholar
• Bowden GT, Kasunic M, Sim D. Sequence dependence for the hyperthermic potentiation of cis-diaminedichloroplatinum (II) induced cytotoxicity and DNA damage. In: NAHG Annual Meeting; 1983, San Antonio: NAHG, 1983: 161–2.
   Google Scholar
• Douple EB, Strahbehn JW, Desieyes DC, Alborough DP. Therapeutic potentiation of cis-diaminedichloroplatinum and radiation by interstitial microwave hyperthermia in a mouse tumor. Natl Cancer Inst Monogr 1982; 61: 259–62.
   Google Scholar
• Engelhardt R. Hyperthermia and drugs. Recent Results Cancer Res 1987; 104: 136–203.
   PubMedGoogle Scholar
• Raaphorst GP, Chabot P, Doja S, Wilkins D, Stewart D, Ng CE. Effect of hyperthermia on cisplatin sensitivity in human glioma and ovarian carcinoma cell lines resistant and sensitive to cisplatin treatment. Int J Hyperthermia 1996; 12: 211–22.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Doja S, Davis L, Stewart D, Ng CE. A comparison of hyperthermia cisplatin sensitization in human ovarian carcinoma and glioma cell lines sensitive and resistant to cisplatin treatment. Cancer Chernother Pharrnacol 1996; 37: 574–80.
   Google Scholar
• Urano M, Kahn J, Kenton LA. The effect of cis-diamminedichloroplatinum(II) treatment at elevated temperatures on murine fibrosarcoma, FSa-II. Int J Hyperthermia 1990; 6: 563–70.
   Google Scholar
• Carde P, Laval F. Effect of cis-dichlorodiammine platinum II and X rays on mammalian cell survival. Int J Radiat Oncol Biol Phys 1981; 7: 929–33.
   PubMed Web of Science ®Google Scholar
• Douple EB. Interaction between cisplatin coordination complexes and radiation. In: Hill BT, Bellamy AS, eds, Antitumor Drug-radiation Interactions. Boca Raton: CRC Press, 1990: 171–90.
   Google Scholar
• Dritschilo A, Piro AJ, Kelman AD. The effect of cis-platinum on the repair of radiation damage in plateau phase Chinese hamster (V-79) cells. Int J Radiat Oncol Biol Phys 1979; 5: 1345–9.
   Google Scholar
• Li GC, Evans RG, Hahn GM. Modification and inhibition of repair of potentially lethal x-ray damage by hyperthermia. Radiat Res 1976; 67: 491–501.
   Google Scholar
• Murthy AK, Harris JR, Belli JA. Hyperthermia and radiation response of plateau phase cells. Potentiation and radiation damage repair. Radiat Res 1977; 70: 241–7.
   Google Scholar
• Raaphorst GP, Freeman ML, Dewey WC. Radiosensitivity and recovery from radiation damage in cultured CHO cells exposed to hyperthermia at 42.5 or 45.5 degrees C. Radiat Res 1979; 79: 390–402.
   Google Scholar
• Raaphorst GP. Recovery of sublethal radiation damage and its inhibition by hyper-thermia in normal and transformed mouse cells. Int J Radiat Oncol Biol Phys 1992; 22: 1035–41.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Feeley MM, Danjoux CE, DaSilva V, Gerig LH. Hyperthermia enhance-ment of radiation response and inhibition of recovery from radiation damage in human glioma cells. Int J Hyperthermia 1991; 7: 629–41.
   Google Scholar
• Wilkins DE, Heller DP, Raaphorst GP. Inhibition of potentially lethal damage recovery by cisplatin in a brain tumor cell line. Anticancer Res 1993; 13: 2137–42.
   Google Scholar
• Raaphorst GP, Miao J, Ng CE. Cisplatin and mild hyperthermia in radiosensitization to low dose rate irradiation in human ovarian carcinoma cells. Anticancer Res 1997; 17: 3469–72.
   Google Scholar
• Raaphorst GP, Miao J, Stewart D, Ng CE. Interactions of mild hyperthermia, cisplatin and split dose irradiation in human ovarian carcinoma cells. Cancer Chernother Pharmacol 1998; 41: 491–6.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Yang H, Wilkins DE, Ng CE. Cisplatin, hyperthermia and radiation treatment in human cisplatin-sensitive and resistant glioma cell lines. Int J Hypertherrnia 1996; 12: 801–12.
   PubMed Web of Science ®Google Scholar
• Raaphorst GP, Miao J, Ng CE, Stewart DJ. Concomitant treatment with mild hyperthermia, cisplatin and low dose rate irradiation in human ovarian cancer cells sensitive and resistant to cisplatin. Oncol Rep 1998; 5: 971–7.
   PubMed Web of Science ®Google Scholar
• Feyerabend T, Steeves R, Wiedemann GJ, Richter E, Robins HI. Rationale and clinical status of local hyperthermia, radiation, and chemotherapy in locally advanced malig-nancies. Anticancer Res 1997; 17: 2895–7.
   Google Scholar
• Herman TS, Teicher BA. Sequencing of trimodality therapy [cis-diamminedichloro-platinum(H)/hyperthermia/radiation] as determined by tumor growth delay and tumor cell survival in the FSaIIC fibrosarcoma. Cancer Res 1988; 48: 2693–7.
   PubMed Web of Science ®Google Scholar
• Herman TS, Jochelson MS, Teicher BA, Scott RI, Hansen J, Clark JR, Pfeffer MR, Gelwan LE, Molnar-Griffin B, Fraser SM, Svennson G, Bornstein BA, Ryan L, Coleman CN. A phase I—II trial of cisplatin, hyperthermia and radiation in patients with locally advanced malignancies. Int J Radiat Oncol Biol Phys 1989; 17: 1273–9.
   PubMed Web of Science ®Google Scholar
• Jones EL, Dewhirst MW, Samulski TV, Prosnitz LR. A pilot study of cisplatin, hyperthermia and radiotherapy for locally advanced cervical cancer; two promising combinationsno definite conclusions. Cancer 2003; 98: 277–8.
   PubMed Web of Science ®Google Scholar
• Prosnitz L, Jones E. Counterpoint: test the value of hyperthermia in patients with carcinoma of the cervix being treated with concurrent chemotherapy and radiation. Int J Hypertherrnia 2002; 18: 13–18.
   PubMed Web of Science ®Google Scholar
• Van der Zee J, Koper PC, Lutgens LC, Burger CW. Point-counterpoint: what is the optimal trial design to test hyperthermia for carcinoma of the cervix? Point: addition of hyperthermia or cisplatin to radiotherapy for patients with cervical cancer; two promising combinationsno definite conclusions. Int J Hypertherrnia 2002; 18: 19–24.
   PubMed Web of Science ®Google Scholar