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DOI:10.2214/AJR.06.1281
AJR 2007; 189:140-144
© American Roentgen Ray Society


Original Research

Recurrent Cancer After Breast-Conserving Surgery with Radiation Therapy for Ductal Carcinoma in Situ: Mammographic Features, Method of Detection, and Stage of Recurrence

Renee W. Pinsky1, Murray Rebner2, Lori J. Pierce3, Merav A. Ben-David3,4, Frank Vicini5, Karen A. Hunt1,6 and Mark A. Helvie1

1 Department of Radiology, University of Michigan Health System, 1500 E Medical Center Dr., Ann Arbor, MI 48109-0302.
2 Department of Radiology, William Beaumont Hospital, Royal Oak, MI.
3 Department of Radiation Oncology, University of Michigan Health System, Ann Arbor, MI.
4 Present address: Oncology Department, Radiation Oncology Unit, Sheba Medical Center, Ramat-Gan, Israel.
5 Department of Radiation Oncology, William Beaumont Hospital, Royal Oak, MI.
6 Present address: Department of Radiology, Henry Ford Hospital, West Bloomfield, MI.

Received September 27, 2006; accepted after revision January 26, 2007.

 
Address correspondence to R. W. Pinsky (rpinsky{at}umich.edu).


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The purpose of our study was to determine the mammographic appearance, detection method, and stage of ipsilateral breast tumor recurrence in women treated with breast-conserving surgery and whole-breast radiation therapy for ductal carcinoma in situ (DCIS).

MATERIALS AND METHODS. Following institutional review board approval, records of women treated with breast-conserving surgery and radiation therapy for DCIS who developed an ipsilateral breast tumor recurrence from 1981 to 2003 were reviewed retrospectively. Multiinstitutional database records showed 513 women were treated, of whom 42 (8.2%) developed local recurrence. Study criteria were fulfilled and complete records were available for 32 women. Mean age at initial diagnosis was 49 years (range, 26-73 years).

RESULTS. Of the 32 patients included in our study, 31 (97%) recurrences were mammographically apparent. Twenty-nine (91%) of 32 were diagnosed exclusively by mammography. Mammographic findings at recurrence were calcifications in 24 (75%) of 32, mass in six (19%) of 32, and distortion in one (3%) of 32. The mean time to recurrence was 4.5 years. Twelve (40%) of 30 had the recurrence in a remote quadrant from the original cancer. Recurrences were DCIS in 17 (53%) of 32, DCIS with microinvasion in six (19%) of 32, invasive ductal cancer in three (9%) of 32, invasive lobular cancer in two (6%) of 32, and mixed DCIS and invasive cancer in four (13%) of 32. Six (67%) of nine patients with invasive cancer (excluding microinvasion) had tumors smaller than 1 cm. Ninety-one percent of recurrences were minimal cancers. All recurrences were stage 0 or 1.

CONCLUSION. Mammography successfully detected ipsilateral breast tumor recurrence, predominantly as calcifications or masses, after breast-conserving surgery with radiation therapy for DCIS in 97% of cases. The recurrences were located at variable distances from the lumpectomy site. Ninety-one percent of recurrences were minimal cancers and all were early stage, connoting excellent prognosis.

Keywords: breast • breast cancer • cancer recurrence • DCIS • ductal carcinoma in situ • mammography • women's imaging


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Women newly diagnosed with ductal carcinoma in situ (DCIS) of the breast face a perplexing array of treatment options ranging from mastectomy with hormonal therapy to lumpectomy alone. Although multiple randomized controlled trials have documented the equivalency of lumpectomy and radiation therapy to that of mastectomy in terms of survival for invasive breast cancer, DCIS is less well studied. Hence, clinical decisions regarding "best" treatment are based on nonuniform and nonrandomized trials.

Mastectomy for DCIS has been associated with a long-term local regional disease-free survival of 95% or greater [1-5]. Although breast conservation surgery with whole-breast radiation therapy has proven to be effective, women electing this treatment are faced with the prospect of a local regional recurrence rate of approximately 1% per year [6]. This decreases with the addition of tamoxifen in selected women [7, 8]. Although many consider mastectomy to be curative, a small percentage of patients (1-4%) will eventually develop chest wall recurrence [1-5]. These recurrences are usually invasive carcinomas that are detected once they are palpable. Because the rate of local recurrence with lumpectomy and breast radiation is higher than with mastectomy, it is important for a woman electing this treatment path to understand not only the risk of recurrence but also the implications of a recurrence. We therefore reviewed our data of women experiencing a local recurrence after breast-conserving surgery and radiation therapy. We were particularly interested to observe the radiographic appearance, method of detection, location of recurrence, and, most important, the size and stage of recurrence that would provide information regarding prognosis after recurrence. This information should be helpful in guiding radiologists, oncologists, and patients facing treatment decisions and planning surveillance methods when breast conservation is chosen.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Institutional review board approval was obtained from both study institutions. Written informed consent was not required for this retrospective study.

Study Population
We performed a retrospective review of women treated for DCIS with breast-conserving surgery and whole-breast radiation therapy who subsequently developed an ipsilateral breast tumor recurrence. Breast imaging studies and medical records, including demographic and pathology records, were analyzed. Local recurrence was defined as the presence of cancer anywhere in the treated breast. The study population was gathered from the radiation oncology databases from two hospitals, one a large, academic, National Cancer Institute-designated comprehensive cancer center and the other a large private teaching hospital. The databases were searched for cases in which the initial cancer and recurrence occurred between January 1986 and December 2003 at one institution and between January 1981 and December 2003 at the other. All initial cancers were primary unifocal DCIS, stage 0 according to the American Joint Committee on Cancer (AJCC) staging system, version 5 [9]. No microinvasion was present on histopathology.

A total of 513 women were treated with breast-conserving surgery and radiation therapy for DCIS at the two institutions during the study period. Of these women, 42 developed local recurrence (crude recurrence rate, 8.2%). Complete records, including mammograms (or detailed mammographic reports) and medical records, were available for the 32 patients who constitute our study population. Seven patients were excluded for lack of mammogram data or incomplete medical records. Three were excluded for initial presentation with multicentric DCIS.

In both centers, whole-breast radiation therapy was delivered using two opposed tangential fields. All patients were treated with megavoltage radiation, generally 6 MV, to a dose of 45-50 Gy in 1.8- to 2.0-Gy fractions over 4.5-5 weeks; a supplemental boost to the tumor bed, usually administered using electrons, was delivered in most cases. The median total tumor bed dose was approximately 60 Gy at both institutions. No regional lymphatic radiation was delivered. Specific treatment details for both centers are described elsewhere [10, 11].

Mammography and Imaging Assessment
The routine for imaging included physician-monitored diagnostic mammography for all of the initial DCIS studies, including magnification views for calcifications. For women with tumor-associated calcifications on the diagnostic mammogram, a postlumpectomy mammogram was performed to identify residual calcifications. Mammographic evaluation of the affected breast after lumpectomy and radiation therapy at one of the institutions included craniocaudal, mediolateral oblique, and lateral views and a magnification view of the lumpectomy site at 6 months, a bilateral mammogram with a magnification view of the lumpectomy site at 12 and 24 months, and then bilateral mammograms annually. At the second institution, a similar protocol was followed, omitting the lateral view at 6 months and adding a second magnification view of the lumpectomy site at 12 and 24 months. MRI and whole-breast sonography were not routinely performed at the time of diagnosis or as part of an annual surveillance. Digital mammography was not used. Compliance was not analyzed in this study. All cases of recurrence were presented at a multidisciplinary tumor board conference that included breast radiologists, surgeons, medical oncologists, radiation oncologists, nurses, and other support staff.

The mammograms and clinical information were reviewed by two Mammography Quality Standards Act-certified radiologists with 14 and 22 years of experience in mammographic interpretation. A recurrence was defined as the second occurrence of cancer in the treated breast. Original mammogram films were used when available. Alternatively, detailed mammography reports were used if they contained information regarding method of detection, location, size, and mammographic appearance of the recurrence. Mammographic findings on the initial and recurrence images were classified as calcifications, mass plus calcifications, mass alone, distortion, asymmetry, edema, and negative examination. Calcifications were categorized as amorphous and indistinct, coarse and heterogeneous, pleomorphic, or linear and branching. When it was available, the BI-RADS final assessment category was recorded [12]. The distance from the site of the primary cancer was measured or estimated from the lumpectomy site when original films were not available for review. The quadrant and distance from the nipple were identified for both the initial and recurrent carcinomas. The method of presentation (mammographic, palpable, nipple discharge, or other) of both the original and the recurrent cancers was recorded.

Pathologic Assessment
The pathologic results of the recurrent cancers were recorded from the medical record. These diagnoses were categorized as DCIS, DCIS with microinvasion, invasive ductal cancer, invasive lobular cancer, or other invasive cancer. Microinvasion was defined as DCIS with an invasive component of 0.1 cm or less [9]. Lobular carcinoma in situ was not considered malignant. When available, the type and grade of DCIS and the presence or absence of axillary lymph node metastases and angiolymphatic invasion were recorded. The size of the recurrent cancer was based on pathologic size in the medical record. When this was not available, the mammographic size of the abnormality was used as the size of the recurrence. A tumor recurrence was further characterized as minimal cancer if it was noninvasive or, if invasive, as measuring 1 cm or less [13]. The status of the original surgical margins was described as positive, negative, or close. A close margin was defined as DCIS less than 3 mm from the inked margin.

Clinical Assessment
The time to recurrence was calculated from the date of initial diagnosis to date of recurrence. Time to recurrent DCIS versus invasive recurrence was compared. Time to recurrence in the same quadrant and elsewhere in the breast was analyzed as well. Tamoxifen use was not analyzed.

Statistics
Two-sample Student's t tests were used to determine the significance between the interval to a noninvasive recurrence versus an invasive recurrence and the interval to recurrence in the same quadrant versus recurrence elsewhere in the breast. A difference with a p value of less than 0.05 was considered significant.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Five hundred thirteen women were treated with lumpectomy and radiation therapy for DCIS. Of these women, 42 developed local recurrence, a crude recurrence rate of 8.2%. The mean age at the time of the initial DCIS diagnosis was 49 years (range, 26-73 years).

Thirty-two of the 42 patients with recurrence had adequate medical and radiographic records and unifocal DCIS, and they constitute our study population. Thirty-one (97%) of 32 cancer recurrences were mammographically visible. Twenty-nine (91%) were exclusively diagnosed on mammography. Two (6%) were diagnosed by both palpation and mammography, and one (3%) was diagnosed by visual inspection with a normal mammogram (Paget's disease). The two recurrent cases that were palpable were invasive cancer.

Original mammogram films were available for review in 28 (88%) of 32 patients. The mammographic appearances of the initial and recurrent cancer are detailed in Table 1. Seventy-five percent of recurrences presented mammographically as microcalcifications, and 18% presented as masses on the mammogram. The calcifications of the primary DCIS were all pleomorphic or of the linear branching type. Morphologic analysis of the calcifications was possible for 22 (92%) of 24 calcification-containing recurrences. Twenty-one (95%) were either pleomorphic or of the linear branching type. One (5%) was in the amorphous indistinct category. Eighty percent of the patients who presented initially with microcalcifications had a recurrence manifested by microcalcifications. The appearance of the calcifications in both the initial and recurrent tumors was available in 18 patients. In 17 (94%) of 18 patients, the recurrent tumor calcifications had a morphology similar to the initial DCIS (Figs. 1A, 1B, and 1C).


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TABLE 1: Mammographic Appearance of Initial Ductal Carcinoma in Situ (DCIS) and Recurrent Tumor

 

Figure 1
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Fig. 1A 43-year-old woman developed pleomorphic microcalcifications on follow-up mammography 7 years after breast-conserving surgery and radiation therapy for ductal carcinoma in situ (DCIS). Her recurrence was invasive lobular carcinoma, with lobular carcinoma in situ located 9 cm from original lumpectomy site in same quadrant. Mediolateral oblique mammogram at time of recurrence. Surgical clips indicate lumpectomy bed. Circle indicates site of recurrence.

 

Figure 2
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Fig. 1B 43-year-old woman developed pleomorphic microcalcifications on follow-up mammography 7 years after breast-conserving surgery and radiation therapy for ductal carcinoma in situ (DCIS). Her recurrence was invasive lobular carcinoma, with lobular carcinoma in situ located 9 cm from original lumpectomy site in same quadrant. Spot magnification view of primary DCIS at time of wire localization shows microcalcifications.

 

Figure 3
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Fig. 1C 43-year-old woman developed pleomorphic microcalcifications on follow-up mammography 7 years after breast-conserving surgery and radiation therapy for ductal carcinoma in situ (DCIS). Her recurrence was invasive lobular carcinoma, with lobular carcinoma in situ located 9 cm from original lumpectomy site in same quadrant. Spot magnification view of recurrence also shows microcalcifications.

 

Recurrences were pure DCIS in 17 (53%) of 32 (including one case of Paget's disease with DCIS), DCIS with microinvasion in six (19%) of 32, invasive ductal carcinoma in three (9%) of 32, invasive lobular carcinoma in two (6%) of 32, and DCIS with invasive cancer in four (13%) of 32. Seventeen of the recurrences (53%) were stage 0 and 15 (47%) were stage 1. Of the 15 patients with an invasive recurrence, 12 (80%) measured less than 1 cm. Overall, the recurrences were minimal cancers in 29 (91%) of 32 patients. Excluding cases of microinvasion, the median and mean sizes of the invasive cancers were 0.8 and 1.1 cm, respectively (range, 0.5-2.0 cm). None of 15 invasive carcinomas had angiolymphatic invasion. Seven patients with invasive cancer and two with pure DCIS had lymph node sampling at the time of the recurrence, and all were negative for metastasis.

The mean distance between the initial and the recurrent cancers was 3.8 cm (median, 3.5 cm; range, 0-9 cm) in 30 patients for whom these data were available. Eighteen (60%) of 30 patients had their recurrence in the same quadrant as the original DCIS (Figs. 1A, 1B, 1C, and 2).


Figure 4
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Fig. 2 50-year-old woman with recurrence presenting as microcalcifications 3 years after treatment. Magnification of mediolateral oblique view of lumpectomy site shows clips and scar. Note new pleomorphic microcalcifications nearby. These microcalcifications were ductal carcinoma in situ with microinvasion located 2 cm from lumpectomy site.

 
Of 26 patients with available margin status before radiation therapy, 16 had negative margins, nine had close margins, and one patient had positive margins.

The mean time to recurrence for all patients was 4.5 years. See Figure 3 for distribution of frequency of time to recurrence. No significant difference was seen in time to recurrence between noninvasive and invasive cancers (3.8 and 5.2 years, respectively) (p = 0.14). However, a trend was seen toward longer time to an invasive recurrence. No significant difference was seen in the mean time to recurrence in the same quadrant versus mean time to recurrence elsewhere in the breast (4.9 vs 4.1 years) (p = 0.42).


Figure 5
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Fig. 3 Time interval (in years) from initial diagnosis of ductal carcinoma in situ to recurrence versus percentage of total patients.

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Women treated for DCIS with breast-conserving surgery and radiation therapy can expect a low rate of recurrent disease. In our study, mammography was effective at detecting recurrence, with 97% of cases detected on mammography. When cancer did recur, 91% were minimal cancers and all were stage 0 or 1. This provides inferential support for excellent prognosis even when recurrence does occur. For the radiologist, the appearance of the recurrence and follow-up imaging strategies are paramount.

The crude recurrence rate of 8.2% confirms the low rate of tumor recurrence after breast-conserving surgery with radiation therapy. Several studies have addressed the rate of local recurrence after the various treatment options for DCIS [3, 4, 10, 14-17]. In the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-17 trial, local recurrence rates after breast-conserving surgery and radiation therapy were reported to be 7% at 5 years and 12% at 8 years [14, 17, 18]. The European Organization for Research and Treatment of Cancer (EORTC) trials confirmed reduced recurrence rates with radiation therapy, reporting 10-year local recurrence rates of 14.8% for the group treated with radiation and 26% for the group treated with lumpectomy alone (p < 0.0001) [19]. The United Kingdom Coordinating Committee on Cancer Research (UKCCCR) study showed 5-year ipsilateral recurrence rates of 6% for the radiation therapy group versus 14% for the group with lumpectomy alone (p < 0.0001) [20].

Mastectomy is an alternative treatment option for DCIS; however, it does not completely eliminate the risk of local recurrence. The incidence of locally recurrent cancer after mastectomy for DCIS has been variably reported as 1-4% for follow-up periods of 5-9 years [2-6]. These recurrences occur in the form of chest wall recurrences, and typically are invasive cancers detected by palpation because mammographic evaluation is not performed [1, 4].

As screening mammography has become standard practice, the incidence of DCIS has increased. It is estimated to represent 22% of all breast cancers diagnosed in the United States in 2005 [21]. The American Cancer Society estimates of the annual incidence of DCIS has increased from 30,000 in 1996 to more than 58,000 in 2005. Just as the initial diagnosis of DCIS is primarily made mammographically, recurrences are also primarily detected mammographically. Postsurgical and postirradiation changes may diminish mammographic sensitivity [22, 23]. Postoperative seroma, hematoma, scarring, and edema can alter the density and architecture of the breast. Progressively better mammography, regular use of magnification views of the lumpectomy site before radiation therapy, a baseline study after radiation therapy, routine follow-up mammograms, and better surgical and radiation therapy techniques resulting in less deformity [22] may enhance our ability to detect suspicious changes in the breast.

Most patients who presented with calcifications in the original DCIS had recurrences with calcifications. The finding of new suspicious calcifications on a follow-up mammogram should prompt a biopsy. Similarity in morphology between the primary and recurrent calcifications was seen in 94% of these patients. We consider this an aid for the radiologist in assessing follow-up studies, which underscores the value of having prior films for comparison.

The prognosis of breast cancer is closely tied to its stage at the time of diagnosis. In our study, all recurrences were diagnosed as an AJCC stage 0 or 1. The high percentage of recurrence as DCIS (53%) and as minimal breast cancer (91%) predicts an excellent prognosis [24]. Orel et al. [25] reported a statistically significant association between detection of a tumor recurrence on mammography alone and a lower tumor stage after treatment for earlystage invasive breast cancers. A trend was also noted toward noninvasive histology and longer disease-free survival.

In our study, only 60% of the recurrences occurred in the same quadrant and 40% recurred elsewhere in the breast. Tumor recurrence has previously been reported to occur with greatest frequency at or close to the lumpectomy site [2, 26]. Fisher et al. [17] reported early results of the NSABP B-17 trial, in which 84% of recurrences were in the same quadrant of the breast or at the border of the quadrant. In a study by Liberman et al. [26] of breast-conserving surgery for DCIS, 90% of the recurrences occurred in the same quadrant. We found no significant difference between the time to recurrence in the same quadrant and time to recurrence elsewhere in the breast. The former was 4.9 years and the latter was 4.1 years (p = 0.42).

In our study, all recurrences occurred after 1 year from the date of diagnosis. The mean time between the initial and recurrent cancers was 4.5 years (range, 1-12 years), with a clustering between 1 and 7 years. This time interval is longer than the mean time to recurrence of 2.8 years reported by Weng et al. [3] in a similar treatment group. In a multiinstitutional study reported by Solin et al. [27], mean time to recurrence was 5.7 years. These studies suggest that long-term mammographic surveillance is necessary after breast-conserving surgery and radiation therapy for women diagnosed with DCIS. However, Doubeni et al. [28] showed that the percentage of breast cancer survivors having regular mammograms declines with time after diagnosis.

Our study has several potential limitations. Because all patients had whole-breast radiation therapy, these results may not apply to patients who were treated with lumpectomy alone or with partial breast irradiation. None of the patients had clinical MRI or whole-breast sonography to locate other primary or residual disease. The impact of these tests on detecting future recurrence is unknown. The use of mammography reports when actual films were not available may have introduced a measurement error. It was necessary in some cases to use the mammographic size of a lesion, which is not considered as accurate as a pathologic measurement. Tamoxifen was not in widespread use during a large part of this study period. Studies have shown the expected recurrence rate is lower with the use of tamoxifen as adjuvant treatment after radiation therapy [8]. Postlumpectomy mammography was routinely used in this study to identify residual disease. Institutions that do not perform postlumpectomy mammography may experience different outcomes. Women at both centers were evaluated at comprehensive breast centers using multidisciplinary approaches to diagnosis and treatment, which may influence the course of treatment.

In conclusion, ipsilateral breast tumor recurrence after breast-conserving surgery and radiation therapy for DCIS was an infrequent event. Mammography was highly effective at detecting early tumor recurrence, with 97% presenting with an abnormal mammogram. Ninety-one percent of recurrences were minimal cancers at detection, suggesting an excellent prognosis even when tumors recur.


References
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Silverstein MJ, Barth A, Poller DN, et al. Ten-year results comparing mastectomy to excision and radiation therapy for ductal carcinoma in situ of the breast. Eur J Cancer 1995;31A : 1425-1427[CrossRef]
  2. Burstein HJ, Polyak K, Wong JS, Lester SC, Kaelin CM. Ductal carcinoma in situ of the breast. N Engl J Med2004; 350:1430 -1441[Free Full Text]
  3. Weng EY, Juillard GJ, Parker RG, Chang HR, Gornbein JA. Outcomes and factors impacting local recurrence of ductal carcinoma in situ. Cancer 2000; 88:1643 -1649[CrossRef][Medline]
  4. Vargas C, Kestin L, Go N, et al. Factors associated with local recurrence and cause-specific survival in patients with ductal carcinoma in situ of the breast treated with breast-conserving therapy or mastectomy. Int J Radiat Oncol Biol Phys 2005;63 : 1514-1521[CrossRef][Medline]
  5. Warneke J, Grossklaus D, Davis J, et al. Influence of local treatment on the recurrence rate of ductal carcinoma in situ. J Am Coll Surg 1995; 180:683 -688[Medline]
  6. Harris J, Morrow M, Osborne C, Lippman M. Diseases of the breast, 3rd ed. Philadelphia, PA: Lippincott Williams & Wilkins, 2004: 525
  7. Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for the prevention of breast cancer: current status of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst2005; 97:1652 -1662[Abstract/Free Full Text]
  8. Fisher B, Dignam J, Wolmark N, et al. Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial. Lancet1999; 353:1993 -2000[CrossRef][Medline]
  9. Greene FL, Page DL, Fleming ID, et al., eds. AJCC cancer staging handbook. From the AJCC cancer staging manual, 6th ed. New York, NY: Springer-Verlag, 2002:255 -281
  10. Kestin LL, Goldstein NS, Martinez AA, et al. Mammographically detected ductal carcinoma in situ treated with conservative surgery with or without radiation therapy: patterns of failure and 10-year results. Ann Surg 2000;231 : 235-245[CrossRef][Medline]
  11. Ben-David MA, Griffith KA, Hayman JA, Lichter AS, Pierce LJ. Long-term results of conservative surgery and radiotherapy using lung density correction of ductal carcinoma in situ. (abstr) Proceedings of the American Society of Therapeutic Radiology and Oncology (ASTRO), 2006. Fairfax, VA: ASTRO, 2006
  12. American College of Radiology. Breast Imaging Reporting and Data System, 3rd ed. Reston, VA: ACR,1998
  13. Bassett L, Hendrick R, Bassford T. Quality determinants of mammography. In: Clinical practice guideline, number 13. Rockville, MD: U.S. Department of Health and Human Services,1994
  14. Fisher B, Costantino J, Redmond C, et al. Lumpectomy compared with lumpectomy and radiation therapy for the treatment of intraductal breast cancer. N Engl J Med 1993;328 : 1581-1586[Abstract/Free Full Text]
  15. Solin LJ, Fourquet A, Vicini FA, et al. Salvage treatment for local recurrence after breast-conserving surgery and radiation as initial treatment for mammographically detected ductal carcinoma in situ of the breast. Cancer 2001; 91:1090 -1097[CrossRef][Medline]
  16. Jha MK, Avlonitis VS, Griffith CD, et al. Aggressive local treatment for screen-detected DCIS results in very low rates of recurrence. Eur J Surg Oncol 2001;27 : 454-458[CrossRef][Medline]
  17. Fisher B, Dignam J, Wolmark N, et al. Lumpectomy and radiation therapy for the treatment of intraductal breast cancer: findings from National Surgical Adjuvant Breast and Bowel Project B-17. J Clin Oncol 1998; 16:441 -452[Abstract]
  18. Fisher ER, Dignam J, Tan-Chiu E, et al. Pathologic findings from the National Surgical Adjuvant Breast Project (NSABP) eight-year update of protocol B-17: intraductal carcinoma. Cancer1999; 86:429 -438[CrossRef][Medline]
  19. Bijker N, Meijnen P, Peterse JL, et al. Breast-conserving treatment with or without radiotherapy in ductal carcinoma-in-situ: ten-year results of European Organisation for Research and Treatment of Cancer randomized phase III trial 10853—a study by the EORTC Breast Cancer Cooperative Group and EORTC Radiotherapy Group. J Clin Oncol2006; 24:3381 -3387[Abstract/Free Full Text]
  20. Houghton J, George WD, Cuzick J, Duggan C, Fentiman IS, Spittle M. Radiotherapy and tamoxifen in women with completely excised ductal carcinoma in situ of the breast in the UK, Australia, and New Zealand: randomised controlled trial. Lancet 2003;362 : 95-102[CrossRef][Medline]
  21. Estimated new cancer cases and deaths by sex for all sites, US,2005 . American Cancer Society Website. Available at: www.cancer.org/docroot/MED/content/downloads/MED_1_1x_CFF2005_Estimated_New_Cases_Deaths_by_Sex_US.asp. Accessed June 8, 2006
  22. Giess CS, Keating DM, Osborne MP, Rosenblatt R. Local tumor recurrence following breast-conservation therapy: correlation of histopathologic findings with detection method and mammographic findings. Radiology 1999;212 : 829-835[Abstract/Free Full Text]
  23. Dershaw DD. Mammography in patients with breast cancer treated by breast conservation (lumpectomy with or without radiation). AJR 1995; 164:309 -316[Abstract/Free Full Text]
  24. Wirman JA. The clinical significance of minimal breast cancer: a pathologist's viewpoint. Crit Rev Oncol Hematol1985; 3:35 -74[Medline]
  25. Orel SG, Fowble BL, Solin LJ, Schultz DJ, Conant EF, Troupin RH. Breast cancer recurrence after lumpectomy and radiation therapy for early-stage disease: prognostic significance of detection method. Radiology 1993;188 : 189-194[Abstract/Free Full Text]
  26. Liberman L, Van Zee KJ, Dershaw DD, Morris EA, Abramson AF, Samli B. Mammographic features of local recurrence in women who have undergone breast-conserving therapy for ductal carcinoma in situ. AJR 1997; 168:489 -493[Abstract/Free Full Text]
  27. Solin LJ, Fourquet A, Vicini FA, et al. Mammographically detected ductal carcinoma in situ of the breast treated with breast-conserving surgery and definitive breast irradiation: long-term outcome and prognostic significance of patient age and margin status. Int J Radiat Oncol Biol Phys 2001; 50:991 -1002[CrossRef][Medline]
  28. Doubeni CA, Field TS, Ulcickas Yood M, et al. Patterns and predictors of mammography utilization among breast cancer survivors. Cancer 2006; 106:2482 -2488[CrossRef][Medline]

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