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Erschienen in: Annals of Surgical Oncology 4/2013

01.04.2013 | Bone and Soft Tissue Sarcomas

Long-Term Outcomes in Patients with Radiation-Associated Angiosarcomas of the Breast Following Surgery and Radiotherapy for Breast Cancer

verfasst von: Keila E. Torres, MD, PhD, Vinod Ravi, MD, Katherine Kin, BS, Min Yi, MD, PhD, B. Ashleigh Guadagnolo, MD, MPH, Caitlin D. May, BS, Banu K. Arun, MD, Kelly K. Hunt, MD, Ryan Lam, BS, Guy Lahat, MD, Aviad Hoffman, MD, Janice N. Cormier, MD, MPH, Barry W. Feig, MD, Alexander J. Lazar, MD, PhD, Dina Lev, MD, Raphael E. Pollock, MD, PhD

Erschienen in: Annals of Surgical Oncology | Ausgabe 4/2013

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Abstract

Background

Radiation-associated angiosarcoma (RAAS) is a devastating disease occasionally observed in breast cancer patients treated with radiation. Due to its rarity, our knowledge—of disease risk factors, epidemiology, treatment, and outcome—is extremely limited. Therefore, we sought to identify clinicopathologic factors associated with local and distant recurrence and disease-specific survival (DSS).

Methods

Radiation-associated angiosarcoma was defined as pathologically confirmed breast or chest wall angiosarcoma arising within a previously irradiated field. A comprehensive search of our institutional tumor registry (1/1/93 through 2/28/11) was used to identify patients (n = 95 females). Patient, original tumor, RAAS treatment, and outcome variables were retrospectively retrieved and assembled into a database.

Results

The median follow-up for all RAAS patients was 10.3 (range, 2.4–31.8) years. The latency period following radiation exposure ranged from 1.4 to 26 (median, 7) years. One-year and 5-year DSS rates were 93.5 and 62.6 %, respectively. Reduced risk of local recurrence was observed in patients who received chemotherapy (P = 0.0003). In multivariable analysis, size was found to be an independent predictor of adverse outcome (P = 0.015).

Conclusions

Our study demonstrates that RAAS exhibits high recurrence rates. It also highlights the need for well-designed, multicenter, clinical trials to inform the true utility of chemotherapy in this disease.
Literatur
1.
Zurück zum Zitat Cahan WG, et al. Sarcoma arising in irradiated bone; report of 11 cases. Cancer. 1948;1(1):3–29.PubMedCrossRef Cahan WG, et al. Sarcoma arising in irradiated bone; report of 11 cases. Cancer. 1948;1(1):3–29.PubMedCrossRef
3.
Zurück zum Zitat Majeski J, et al. Cutaneous angiosarcoma in an irradiated breast after breast conservation therapy for cancer: association with chronic breast lymphedema. J Surg Oncol. 2000;74(3):208–12; discussion 212–3. Majeski J, et al. Cutaneous angiosarcoma in an irradiated breast after breast conservation therapy for cancer: association with chronic breast lymphedema. J Surg Oncol. 2000;74(3):208–12; discussion 212–3.
4.
Zurück zum Zitat Monroe AT, et al. Angiosarcoma after breast-conserving therapy. Cancer. 2003;97(8):1832–40.PubMedCrossRef Monroe AT, et al. Angiosarcoma after breast-conserving therapy. Cancer. 2003;97(8):1832–40.PubMedCrossRef
5.
Zurück zum Zitat Taghian A, et al. Long-term risk of sarcoma following radiation treatment for breast cancer. Int J Radiat Oncol Biol Phys. 1991;21(2):361–7.PubMedCrossRef Taghian A, et al. Long-term risk of sarcoma following radiation treatment for breast cancer. Int J Radiat Oncol Biol Phys. 1991;21(2):361–7.PubMedCrossRef
6.
Zurück zum Zitat Tahir M, et al. Radiation induced angiosarcoma a sequela of radiotherapy for breast cancer following conservative surgery. Int Semin Surg Oncol. 2006;3:26.PubMedCrossRef Tahir M, et al. Radiation induced angiosarcoma a sequela of radiotherapy for breast cancer following conservative surgery. Int Semin Surg Oncol. 2006;3:26.PubMedCrossRef
8.
Zurück zum Zitat Yap J, et al. Sarcoma as a second malignancy after treatment for breast cancer. Int J Radiat Oncol Biol Phys. 2002;52(5):1231–7.PubMedCrossRef Yap J, et al. Sarcoma as a second malignancy after treatment for breast cancer. Int J Radiat Oncol Biol Phys. 2002;52(5):1231–7.PubMedCrossRef
9.
Zurück zum Zitat West JG, et al. Risk of angiosarcoma following breast conservation: a clinical alert. Breast J. 2005;11(2):115–23.PubMedCrossRef West JG, et al. Risk of angiosarcoma following breast conservation: a clinical alert. Breast J. 2005;11(2):115–23.PubMedCrossRef
10.
Zurück zum Zitat Pierce SM, et al. Long-term radiation complications following conservative surgery (CS) and radiation therapy (RT) in patients with early stage breast cancer. Int J Radiat Oncol Biol Phys. 1992;23(5):915–23.PubMedCrossRef Pierce SM, et al. Long-term radiation complications following conservative surgery (CS) and radiation therapy (RT) in patients with early stage breast cancer. Int J Radiat Oncol Biol Phys. 1992;23(5):915–23.PubMedCrossRef
11.
Zurück zum Zitat Kirova YM, et al. Radiation-induced sarcomas after radiotherapy for breast carcinoma: a large-scale single-institution review. Cancer. 2005;104(4):856–63.PubMedCrossRef Kirova YM, et al. Radiation-induced sarcomas after radiotherapy for breast carcinoma: a large-scale single-institution review. Cancer. 2005;104(4):856–63.PubMedCrossRef
12.
Zurück zum Zitat Kaplan E, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457–81.CrossRef Kaplan E, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457–81.CrossRef
13.
Zurück zum Zitat Cox DR. Regression models and life tables. J R Stat Soc B. 1972;34:187–220. Cox DR. Regression models and life tables. J R Stat Soc B. 1972;34:187–220.
14.
Zurück zum Zitat Billings SD, et al. Cutaneous angiosarcoma following breast-conserving surgery and radiation: an analysis of 27 cases. Am J Surg Pathol. 2004;28(6):781–8.PubMedCrossRef Billings SD, et al. Cutaneous angiosarcoma following breast-conserving surgery and radiation: an analysis of 27 cases. Am J Surg Pathol. 2004;28(6):781–8.PubMedCrossRef
15.
Zurück zum Zitat Brenn T, Fletcher CD. Radiation-associated cutaneous atypical vascular lesions and angiosarcoma: clinicopathologic analysis of 42 cases. Am J Surg Pathol. 2005;29(8):983–96.PubMed Brenn T, Fletcher CD. Radiation-associated cutaneous atypical vascular lesions and angiosarcoma: clinicopathologic analysis of 42 cases. Am J Surg Pathol. 2005;29(8):983–96.PubMed
16.
Zurück zum Zitat Hui A, et al. Angiosarcoma of the breast: a difficult surgical challenge. Breast. 2012;21(4):584–9.PubMedCrossRef Hui A, et al. Angiosarcoma of the breast: a difficult surgical challenge. Breast. 2012;21(4):584–9.PubMedCrossRef
17.
Zurück zum Zitat Scow JS, et al. Primary and secondary angiosarcoma of the breast: the Mayo Clinic experience. J Surg Oncol. 2010;101(5):401–7.PubMed Scow JS, et al. Primary and secondary angiosarcoma of the breast: the Mayo Clinic experience. J Surg Oncol. 2010;101(5):401–7.PubMed
18.
Zurück zum Zitat Brady MS, et al. Post-treatment sarcoma in breast cancer patients. Ann Surg Oncol. 1994;1(1):66–72.PubMedCrossRef Brady MS, et al. Post-treatment sarcoma in breast cancer patients. Ann Surg Oncol. 1994;1(1):66–72.PubMedCrossRef
19.
Zurück zum Zitat Weatherby RP, et al. Postradiation sarcoma of bone: review of 78 Mayo Clinic cases. Mayo Clin Proc. 1981;56(5):294–306.PubMed Weatherby RP, et al. Postradiation sarcoma of bone: review of 78 Mayo Clinic cases. Mayo Clin Proc. 1981;56(5):294–306.PubMed
20.
Zurück zum Zitat Inoue YZ, et al. Clinicopathologic features and treatment of postirradiation sarcoma of bone and soft tissue. J Surg Oncol. 2000;75(1):42–50.PubMedCrossRef Inoue YZ, et al. Clinicopathologic features and treatment of postirradiation sarcoma of bone and soft tissue. J Surg Oncol. 2000;75(1):42–50.PubMedCrossRef
21.
Zurück zum Zitat Manner J, et al. MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedema. Am J Pathol. 2010;176(1):34–9.PubMedCrossRef Manner J, et al. MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedema. Am J Pathol. 2010;176(1):34–9.PubMedCrossRef
22.
Zurück zum Zitat Hadj-Hamou NS, et al. A transcriptome signature distinguished sporadic from postradiotherapy radiation-induced sarcomas. Carcinogenesis. 2011;32(6):929–34.PubMedCrossRef Hadj-Hamou NS, et al. A transcriptome signature distinguished sporadic from postradiotherapy radiation-induced sarcomas. Carcinogenesis. 2011;32(6):929–34.PubMedCrossRef
23.
Zurück zum Zitat de Jong MA, et al. Reirradiation and hyperthermia for radiation-associated sarcoma. Cancer. 2012;118(1):180–7.PubMedCrossRef de Jong MA, et al. Reirradiation and hyperthermia for radiation-associated sarcoma. Cancer. 2012;118(1):180–7.PubMedCrossRef
24.
Zurück zum Zitat Palta M, et al. Angiosarcoma after breast-conserving therapy: long-term outcomes with hyperfractionated radiotherapy. Cancer. 2010;116(8):1872–8.PubMedCrossRef Palta M, et al. Angiosarcoma after breast-conserving therapy: long-term outcomes with hyperfractionated radiotherapy. Cancer. 2010;116(8):1872–8.PubMedCrossRef
25.
Zurück zum Zitat Riad S, et al. The clinical and functional outcome for patients with radiation-induced soft tissue sarcoma. Cancer. 2012;118(10):2682–92.PubMedCrossRef Riad S, et al. The clinical and functional outcome for patients with radiation-induced soft tissue sarcoma. Cancer. 2012;118(10):2682–92.PubMedCrossRef
26.
Zurück zum Zitat Gladdy RA, et al. Do radiation-associated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas? J Clin Oncol. 2010;28(12):2064–9.PubMedCrossRef Gladdy RA, et al. Do radiation-associated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas? J Clin Oncol. 2010;28(12):2064–9.PubMedCrossRef
27.
Zurück zum Zitat Rao J, et al. Cutaneous angiosarcoma as a delayed complication of radiation therapy for carcinoma of the breast. J Am Acad Dermatol. 2003;49(3):532–8.PubMedCrossRef Rao J, et al. Cutaneous angiosarcoma as a delayed complication of radiation therapy for carcinoma of the breast. J Am Acad Dermatol. 2003;49(3):532–8.PubMedCrossRef
28.
Zurück zum Zitat Fury MG, et al. A 14-year retrospective review of angiosarcoma: clinical characteristics, prognostic factors, and treatment outcomes with surgery and chemotherapy. Cancer J. 2005;11(3):241–7.PubMedCrossRef Fury MG, et al. A 14-year retrospective review of angiosarcoma: clinical characteristics, prognostic factors, and treatment outcomes with surgery and chemotherapy. Cancer J. 2005;11(3):241–7.PubMedCrossRef
29.
Zurück zum Zitat Strobbe LJ, et al. Angiosarcoma of the breast after conservation therapy for invasive cancer, the incidence and outcome. An unforseen sequela. Breast Cancer Res Treat. 1998;47(2):101–9.PubMedCrossRef Strobbe LJ, et al. Angiosarcoma of the breast after conservation therapy for invasive cancer, the incidence and outcome. An unforseen sequela. Breast Cancer Res Treat. 1998;47(2):101–9.PubMedCrossRef
30.
Zurück zum Zitat Pisters PW, et al. Analysis of prognostic factors in 1,041 patients with localized soft tissue sarcomas of the extremities. J Clin Oncol. 1996;14(5):1679–89.PubMed Pisters PW, et al. Analysis of prognostic factors in 1,041 patients with localized soft tissue sarcomas of the extremities. J Clin Oncol. 1996;14(5):1679–89.PubMed
31.
Zurück zum Zitat Zagars GK, et al. Prognostic factors for patients with localized soft-tissue sarcoma treated with conservation surgery and radiation therapy: an analysis of 1225 patients. Cancer. 2003;97(10):2530–43.PubMedCrossRef Zagars GK, et al. Prognostic factors for patients with localized soft-tissue sarcoma treated with conservation surgery and radiation therapy: an analysis of 1225 patients. Cancer. 2003;97(10):2530–43.PubMedCrossRef
32.
Zurück zum Zitat Yang JC, et al. Randomized prospective study of the benefit of adjuvant radiation therapy in the treatment of soft tissue sarcomas of the extremity. J Clin Oncol. 1998;16(1):197–203.PubMed Yang JC, et al. Randomized prospective study of the benefit of adjuvant radiation therapy in the treatment of soft tissue sarcomas of the extremity. J Clin Oncol. 1998;16(1):197–203.PubMed
33.
Zurück zum Zitat Cantin J, et al. The problem of local recurrence after treatment of soft tissue sarcoma. Ann Surg. 1968;168(1):47–53.PubMedCrossRef Cantin J, et al. The problem of local recurrence after treatment of soft tissue sarcoma. Ann Surg. 1968;168(1):47–53.PubMedCrossRef
35.
Zurück zum Zitat Abbas JS, et al. The surgical treatment and outcome of soft-tissue sarcoma. Arch Surg. 1981;116(6):765–9.PubMedCrossRef Abbas JS, et al. The surgical treatment and outcome of soft-tissue sarcoma. Arch Surg. 1981;116(6):765–9.PubMedCrossRef
36.
Zurück zum Zitat Georgiannos SN, Sheaff M. Angiosarcoma of the breast: a 30 year perspective with an optimistic outlook. Br J Plast Surg. 2003;56(2):129–34.PubMedCrossRef Georgiannos SN, Sheaff M. Angiosarcoma of the breast: a 30 year perspective with an optimistic outlook. Br J Plast Surg. 2003;56(2):129–34.PubMedCrossRef
37.
Zurück zum Zitat Penel N, et al. Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study. J Clin Oncol. 2008;26(32):5269–74.PubMedCrossRef Penel N, et al. Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study. J Clin Oncol. 2008;26(32):5269–74.PubMedCrossRef
38.
Zurück zum Zitat Casper ES, et al. Phase II trial of paclitaxel in patients with soft-tissue sarcoma. Cancer Invest. 1998;16(7):442–6.PubMedCrossRef Casper ES, et al. Phase II trial of paclitaxel in patients with soft-tissue sarcoma. Cancer Invest. 1998;16(7):442–6.PubMedCrossRef
39.
Zurück zum Zitat Fata F, et al. Paclitaxel in the treatment of patients with angiosarcoma of the scalp or face. Cancer. 1999;86(10):2034–7.PubMedCrossRef Fata F, et al. Paclitaxel in the treatment of patients with angiosarcoma of the scalp or face. Cancer. 1999;86(10):2034–7.PubMedCrossRef
40.
Zurück zum Zitat Mano MS, et al. Radiation-induced angiosarcoma of the breast shows major response to docetaxel after failure of anthracycline-based chemotherapy. Breast. 2006;15(1):117–8.PubMedCrossRef Mano MS, et al. Radiation-induced angiosarcoma of the breast shows major response to docetaxel after failure of anthracycline-based chemotherapy. Breast. 2006;15(1):117–8.PubMedCrossRef
41.
Zurück zum Zitat Perez-Ruiz E, et al. Response to paclitaxel in a radiotherapy-induced breast angiosarcoma. Acta Oncol. 2009;48(7):1078–9.PubMedCrossRef Perez-Ruiz E, et al. Response to paclitaxel in a radiotherapy-induced breast angiosarcoma. Acta Oncol. 2009;48(7):1078–9.PubMedCrossRef
42.
Zurück zum Zitat Nakamura M, et al. Angiosarcoma with sacral origin metastasizing to the lung. Intern Med. 2006;45(15):923–6.PubMedCrossRef Nakamura M, et al. Angiosarcoma with sacral origin metastasizing to the lung. Intern Med. 2006;45(15):923–6.PubMedCrossRef
43.
Zurück zum Zitat Gambini D, et al. Paclitaxel-dependent prolonged and persistent complete remission four years from first recurrence of secondary breast angiosarcoma. Tumori. 2009;95(6):828–31.PubMed Gambini D, et al. Paclitaxel-dependent prolonged and persistent complete remission four years from first recurrence of secondary breast angiosarcoma. Tumori. 2009;95(6):828–31.PubMed
44.
Zurück zum Zitat Lahat G, et al. Angiosarcoma: clinical and molecular insights. Ann Surg. 2010;251(6):1098–106.PubMedCrossRef Lahat G, et al. Angiosarcoma: clinical and molecular insights. Ann Surg. 2010;251(6):1098–106.PubMedCrossRef
45.
Zurück zum Zitat Lahat G, et al. Outcome of locally recurrent and metastatic angiosarcoma. Ann Surg Oncol. 2009;16(9):2502–9.PubMedCrossRef Lahat G, et al. Outcome of locally recurrent and metastatic angiosarcoma. Ann Surg Oncol. 2009;16(9):2502–9.PubMedCrossRef
46.
Zurück zum Zitat Nagano T, et al. Docetaxel: a therapeutic option in the treatment of cutaneous angiosarcoma: report of 9 patients. Cancer. 2007;110(3):648–51.PubMedCrossRef Nagano T, et al. Docetaxel: a therapeutic option in the treatment of cutaneous angiosarcoma: report of 9 patients. Cancer. 2007;110(3):648–51.PubMedCrossRef
47.
Zurück zum Zitat Silverman LR, et al. Chemotherapy for angiosarcoma of the breast: case report of 30-year survival and analysis of the literature. Cancer Invest. 1994;12(2):145–55.PubMedCrossRef Silverman LR, et al. Chemotherapy for angiosarcoma of the breast: case report of 30-year survival and analysis of the literature. Cancer Invest. 1994;12(2):145–55.PubMedCrossRef
Metadaten
Titel
Long-Term Outcomes in Patients with Radiation-Associated Angiosarcomas of the Breast Following Surgery and Radiotherapy for Breast Cancer
verfasst von
Keila E. Torres, MD, PhD
Vinod Ravi, MD
Katherine Kin, BS
Min Yi, MD, PhD
B. Ashleigh Guadagnolo, MD, MPH
Caitlin D. May, BS
Banu K. Arun, MD
Kelly K. Hunt, MD
Ryan Lam, BS
Guy Lahat, MD
Aviad Hoffman, MD
Janice N. Cormier, MD, MPH
Barry W. Feig, MD
Alexander J. Lazar, MD, PhD
Dina Lev, MD
Raphael E. Pollock, MD, PhD
Publikationsdatum
01.04.2013
Verlag
Springer-Verlag
Erschienen in
Annals of Surgical Oncology / Ausgabe 4/2013
Print ISSN: 1068-9265
Elektronische ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-012-2755-y

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