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Role ofBreast Anthropometry
https://t.me/medicina_free
inOncoplasty andReconstruction
PraveenRoyalMokkapati, ManojGowda, andS.V.S.Deo
10
10.1 Introduction
Breast cancer is the leading cancer among women globally and has replaced cancer cervix as the number one cancer in India. Surgical treatment for breast cancer has witnessed a paradigm shift glob­ally from a predominantly mastectomy based approach to an approach based on breast conserva­tion, oncoplasty, and reconstruction. Breast anthro­pometry including size, shape, ptosis, and nipple areola complex (NAC) anatomy plays an important role in surgical decision making and outcomes. Study of anthropometric data of breast cancer patients from different regions of the world helps evolve individualized surgical decision making guidelines in view of anthropometric variations.
10.2 The Magnitude ofBreast Cancer andIts Impact onWomen
In 2012, there have been 1,671,000 recorded cases of breast cancer worldwide with 145,000 being recorded in India. This has led to 522,000
P. R. Mokkapati (*) Surgical Oncologist, Health Care Global, Vijayawada, India
M. Gowda · S. V. S. Deo Department of Surgical Oncology, AIIMS, New Delhi, India
deaths worldwide and 70,000 deaths in India [1]. The management of breast cancer uses different modalities like surgery, chemotherapy, hormonal therapy, and radiotherapy in various permuta­tions and combinations. The surgical part of the management can broadly be divided into breast conservation surgery with or without oncoplasty and mastectomy with or without reconstruction. Although the human breast biologically has no more purpose after lactation, it has immense social and psychological implications which are evident in the major categories of surgical options. Whether a breast conservation or mas­tectomy is done, proper reconstruction and cos­metic results are paramount.
The female body image is very much inu­enced by the breast in the modern era. The psy­chosocial impact caused by its loss following mastectomy is signicant. With the advent of BREAST-Q score and a holistic approach toward breast cancer, many studies such as those that have been done by Eltahir et al., Andrzejczak etal., and Chao etal. demonstrated the difference in perception of body image, psychosocial and sexual well-being after only mastectomy vs mas­tectomy with reconstruction [24].
Yip etal. did a study on how important was the breast volume symmetry to overall patient satisfaction and found that “process of breast reconstruction,” i.e. the amount of information given to the patient about the postoperative out­comes led to more patient satisfaction than the
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2023 S. V. S. Deo (ed.), Breast Oncoplasty and Reconstruction,
https://doi.org/10.1007/978-981-99-5536-7_10
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actual result of the surgery although it did add value to it [5]. Snell etal. observed the result of clarifying the expectation of patients undergoing breast reconstruction and how it affected patient satisfaction [6]. This is what is being called “real­istic expectations.” However, it is difcult to even reach realistic expectations when there is no information on what a normal breast is. To the best of our knowledge, there have been no reported studies on breast anthropometry in Indian women. Most of the available implants are designed based on Western counterparts.
Sinno et al. [7] did a study on postoperative patient satisfaction in patients who received uni­lateral vs bilateral reconstruction. Patients with bilateral reconstruction rated higher in their satis­faction with symmetry and aesthetics without clothes with a signicant P value. Several meth­ods of breast measurements were used to evalu­ate the aesthetics of a breast which can be used for preoperative planning as well as postopera­tive outcome assessment [816].
10.4 Natural Shape Methods
They estimate the breast volume by using the natural breast contour and include 3D model­ing, thermoplastic casting, and water displace­ment techniques. They use different methods to replicate the natural shape of the breast. In 3D modeling and thermoplastic casting, a mold of the breast in its natural form is made. This is followed with the estimation of volume held by these casts. In water displacement technique, the person is made to position her breasts in a prone position in a water container and the amount of water displaced by them is taken to be the volume of breast. The problem with these methods is that they are cumbersome and assume the posterior border of breast to be a at plane. In addition, water displacement is very uncomfortable and is difcult to maintain the posture required and the posterior wall is dened by plane of the opening of water container.
10.3 Breast Anthropometry
Methods
Breast anthropometry includes the description of breast mainly in terms of its
• Dimensions and volume which include vari-
ous radii and relative position of the nipple
with various landmarks.
Apart from these
• Shape
• Ptosis
• Mammographic density are other parameters
that aid in properly describing breast anthro-
pometry to aid in surgical planning.
Breast volume measurement has been done in a number of ways. They have been classied into
1. Natural shape methods
2. Stereological methods
3. Geometrical methods
4. Mathematical modeling methods [8]
10.5 Stereological Methods
They use a 2D imaging technique like CT-scan or MRI images that are taken with equally spaced slices and then summate them to give the breast volume [8, 10, 14]. Even ultrasound of the breast can be used but it carries the problem of breast compression when the procedure is performed. They are one of the most accurate methods of measuring breast volume because of the exact estimation of the posterior wall. The disadvantages are that they have to be done in a supine position and give only the volume of the breast and not much details of shape of breast in its most socially functional position. CT scans carry additional risk of radiation exposure. MRI also takes a great deal of time. They are very expensive equipment and logistically serve bet­ter for other indications. Having said that, CT scans of chest are done as a part of staging of locally advanced breast cancer and MRI breasts for various decision making dilemmas in early breast cancer. The scans obtained might serve the additional purpose of measuring the breast volume.
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10.6 Geometrical Methods
These methods approximate the shape of breast to a cone or hemisphere or a half ellipsoid and use geometric equations to calculate the breast volume [9, 10, 18, 19]. These formulae are very simple and easy to use. The necessary dimen­sions are obtained by simple tape or ruler mea­surements and substituted in these formulae to give the volume based on the shape of breast assumed. However, like natural displacement methods, they also dene the posterior wall as a at plane. And unlike them, they are less cum­bersome and easier to do. Examples of these methods are using the Grossmann Rounder cast which shapes the breast into a cone and volume of the cone can be obtained from a reading on the cast. Linear equations like the Qiao et al. [17] formula also assume the breast to be a cone to give the breast volume. Breast volume calcu­lated using formula given by Qiao etal. is as follows:
Breast volume = 1/3 × 3.14 × MP2 × (MR+LR+IR– MP) in cubic cm
where MP is mammary projection LR is lateral radius MR is medial radius IR is nipple inframammary fold length
10.7 Mathematical Models
They use formulae derived from polynomial regression to calculate the breast volume [8]. The gold standard of measuring breast volume is by water displacement technique using mastectomy specimens so that the problem of posterior wall is eliminated. Studies have been done to measure cadaveric breast volume or invivo breast with carefully performed water displacement meth­ods. Retrospectively, a formula is devised using polynomial regression to estimate breast volume. An example of this is the Sigurdson’s formula [18]. The problem with this method is that very complicated formulae are obtained and they operate only within the constraints of the cohorts
originally used to devise them. Sigurdson’s for­mula is given by
Breast volume (cc) = 35.5(PP) + 37.7(FP) – 1305
where PP refers to the circumference of the base
of breast
and FP refers to the vertical length from the inframammary fold to the projection of its mid­point on the anterior surface of the breast.
This formula was associated with an adjusted R2 of 0.89, suggesting that 89 percent of volume variability was accounted for by this model. The formula can be applied to only breast volume ranging from 500 to 2400 cc (ideally within 1 standard deviation of mean volume observed in the study with a range from 877cc to 1756 cc). The formula would not be suitable for breasts that lack ptosis because key landmarks are based on the inframammary fold. Furthermore, projec­tion of this fold anteriorly onto the breast can be difcult to evaluate accurately, particularly in women with thick breast bases. A 1-cm differ­ence in the location of this point, for example, would result in a 38-cc change in volume.
10.8 3D Surface Imaging
3D surface imaging for breast anthropometry is a relatively uncharted territory. Images are acquired fast, in whatever position desired, can be repeat­edly measured as a virtual breast can been acquired [8, 13, 1921]. Several techniques have been described and the most commonly used among them are stereophotogrammetry and laser scanning. Two images are recorded from slightly different angles and the coordinates are acquired either manually or automatically by projecting a pattern like a grid on the breast. These instru­ments require dedicated rooms and lighting to provide consistent imaging. They also require frequent calibration. Some of them require xed rigs to help the patient maintain a position while the image is being recorded. Newer generation technology overcomes, to some extent, the need for frequent recalibration and xed rigs. The
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images can be post processed to anticipate opera­tive results. They can also be stored and used postoperatively to compare outcomes. This prop­erty of storage of three- dimensional breast has a huge advantage over other methods as innumer­able measurements can be performed on the breast repeatedly with no patient discomfort. Any anthropometric measurement can be done retro­spectively on the images and compare to any sys­tem of measurement. The instruments have a very low risk of radiation and are less expensive compared to CT-scan or MRI.A number of 3D imaging technologies have been explored for this purpose. Dedicated commercial systems are also available like 3DMD torso, Axis three XT 400, Caneld Vectra XT, Crisalix 3D mammo simula­tor [11, 20, 22]. A number of researchers have also tried the Microsoft Xbox Kinect system [23,
24]. The instrument which has potential for being
used in India is the Faro freestyle 3D scanner. It has a range of 0.5–3m with a maximum lateral resolution of 0.2–1mm and depth resolution of
0.2mm [25]. It is a handheld scanner with a gyro­scope that collects point cloud data from the sub­ject from any position desired.
The human breast has a very dynamic shape and so it has to be measured in the most natural position. A number of linear anthropometric measurements have been dened by Hall etal., Qiao et al., and Dilek et al. to characterize the shape and size of the human breast. Qiao etal. reported the results in Chinese women and Dilek etal. reported them in Turkish women [17, 22]. They used simple anthropometric measures like clavicle-nipple length, sternal notch-nipple length, medial mammary radius, lateral mam­mary radius, etc.
Linear anthropometry uses simple, inexpen­sive, reproducible ways to document various aspects of the human breast. The estimation of breast volume using linear equations or formulae developed by polynomial regression using these parameters is also relatively simple and straight­forward. The patient is also not subjected to any kind of radiation exposure. They individually help in noting postoperative changes also.
10.9 Breast Shape
Breast shape classication has conventionally been done based on the one proposed by Martin and Saller. They have classied it into bowl shaped, hemispherical, conical, and dependent shapes based on the radius and anterior projec­tion of the breast.
• Bowl shaped—anterior projection is less than radius
• Hemispherical—anterior projection is equal to radius
• Conical—anterior projection is greater than radius
• Dependent—nipple is pointing downwards
A new measurement system that has been
given by Eric Swanson is a more objective method to measure the breast shape. However, the system cannot be used with linear anthro­pometry. It requires photographs or 3D imaging [16]. It describes the breast in terms of upper pole and lower pole measures and their relative ratios.
10.10 Ptosis
Breast ptosis is also an important determinant of reconstruction decisions. Renault’s classication of ptosis is the most common type of classica­tion used. It classies ptosis into grade 0,1,2,3 and pseudoptosis.
In grade 0, the nipple should be approximately
2 cm above the inframammary fold. In grade 1 (mild) ptosis, the nipple is at the level of the infra­mammary fold (or approximately 1cm below it).
In grade 2 (moderate) ptosis, the nipple is
approximately 1–3cm below the inframammary fold.
In grade 3 (severe) ptosis, the nipple is approxi-
mately 3cm or more below the inframammary fold.
If the nipple is at a level higher than 3 cm
above the inframammary fold or the lower pole of the breast is located much below the fold, the placement is called pseudoptosis [26].
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10.11 Mammographic Density
Apart from the measurement of the breast in vari­ous dimensions, its density is also an important attribute and has been in most cases measured with the help of a mammogram. The most widely used method is using the BI-RADS system into four categories based on amount of broglandu­lar tissue, with the upper limits of each category being 24%,49%,74%, and 100% [27, 28].
• ACR grade I: 0–24% broglandular tissue
• ACR grade II: 25–49% broglandular tissue
• ACR grade III: 50–74% broglandular tissue
• ACR grade IV: greater than 75% broglandu­lar tissue
Dening the breast in terms of these anthropo-
metric measurements, volume and shape along with 3D surface imaging aids will certainly help acquire a baseline data in Indian cancer patients which can help guide post-mastectomy recon­struction options and in improving the quality of their life.
References
1. GLOBOCAN Cancer Fact Sheets: Breast cancer [Internet]. (cited 2015 Sep 28). Available from: http://
globocan.iarc.fr/old/FactSheets/cancers/breast- new. asp
2. Eltahir Y, Werners LLCH, Dreise MM, van Emmichoven IAZ, Jansen L, Werker PMN, et al. Quality-of-life outcomes between mastectomy alone and breast reconstruction: comparison of patient­reported BREAST-Q and other health-related quality-of-life measures. Plast Reconstr Surg. 2013 Aug;132(2):201e–9e.
3. Andrzejczak E, Markocka-Mączka K, Lewandowski A.Partner relationships after mastectomy in women not offered breast reconstruction. Psychooncology. 2013 Jul 1;22(7):1653–7.
4. Chao L-F, Patel KM, Chen S-C, Lam H-B, Lin C-Y, Liu H-E, et al. Monitoring patient-centered outcomes through the progression of breast recon­struction: a multicentered prospective longitudi­nal evaluation. Breast Cancer Res Treat. 2014 Jun 21;146(2):299–308.
5. Yip JM, Watson DI, Tiggemann M, Hsia S, Smallman AE, Dean NR. Determinants of breast reconstruc­tion outcome: how important is volume symme-
try? J Plast Reconstr Aesthetic Surg JPRAS. 2015 May;68(5):679–85.
6. Snell L, McCarthy C, Klassen A, Cano S, Rubin L, Hurley K, et al. Clarifying the expectations of patients undergoing implant breast reconstruc­tion: a qualitative study. Plast Reconstr Surg. 2010 Dec;126(6):1825–30.
7. Sinno S, Salvino MJ, Vandevender D. Comparing patient satisfaction in bilateral and unilateral breast reconstruction. Plast Surg Nurs. 2014 Sep;34(3):141–5.
8. Xi W, Perdanasari AT, Ong Y, Han S, Min P, Su W, et al. Objective breast volume, shape and surface area assessment: a systematic review of breast mea­surement methods. Aesthet Plast Surg. 2014 Oct 23;38(6):1116–30.
9. Kim MS, Sbalchiero JC, Reece GP, Miller MJ, Beahm EK, Markey MK. Assessment of breast aesthetics. Plast Reconstr Surg. 2008 Apr;121(4):186e–94e.
10. Vedantham S, Shi L, Karellas A, O’Connell AM. Dedicated breast CT: broglandular volume measurements in a diagnostic population. Med Phys. 2012 Dec;39(12):7317–28.
11. Hoeffelin H, Jacquemin D, Defaweux V, Nizet JL.A methodological evaluation of volumetric mea­surement techniques including three-dimensional imaging in breast surgery. Biomed Res Int. 2014 Jan;8(2014):e573249.
12. Veitch DE.Measurement of breast volume using body scan technology (computer-aided anthropometry). Work. 2012;41(1):4038–5.
13. Paulo R, Quieregatto BH. Anthropometry of the breast region: how to measure? Aesthet Plast Surg. 2014;38(2):344–9.
14. Noha Mohamed Osman SMB. Contralateral breast volume measurement during chest CT for postmas­tectomy breast reconstruction. Int J Comput Assist Radiol Surg. 2014;10(2):141–7.
15. Katariya RN, Forrest APM, Gravelle IH. Breast volumes in cancer of the breast. Br J Cancer. 1974 Mar;29(3):270–3.
16. Swanson E.A measurement system for evaluation of shape changes and proportions after cosmetic breast surgery. Plast Reconstr Surg. 2012;129(4):982–92.
17. Qiao Q, Zhou G, Ling Y.Breast volume measurement in young Chinese women and clinical applications. Aesthet Plast Surg. 1997 Sep;21(5):362–8.
18. Sigurdson LJ, Kirkland SA.Breast volume determina­tion in breast hypertrophy: an accurate method using two anthropomorphic measurements. Plast Reconstr Surg. 2006 Aug;118(2):313–20.
19. Jessica B, Chang KHS. 3D surface imaging in plastic surgery: foundation, practical appli­cations, and beyond. Plast Reconstr Surg. 2015;135(5):1295–304.
20. Yip JM, Mouratova N, Jeffery RM, Veitch DE, Woodman RJ, Dean NR. Accurate assessment of breast volume: a study comparing the volumetric gold standard (direct water displacement measurement of
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mastectomy specimen) with a 3D laser scanning tech­nique. Ann Plast Surg. 2012 Feb;68(2):135–41.
21. Greg M, Galdino MN.Clinical applications of three­dimensional photography in breast surgery. Plast Reconstr Surg. 2002;110(1):58–70.
22. Henseler H, Smith J, Bowman A, Khambay BS, Ju X, Ayoub A, etal. Investigation into variation and errors of a three-dimensional breast imaging system using multiple stereo cameras. J Plast Reconstr Aesthet Surg. 2012 Dec 1;65(12):e332–7.
23. Henseler H, Kuznetsova A, Vogt P, Rosenhahn B. Validation of the Kinect device as a new por­table imaging system for three-dimensional breast assessment. J Plast Reconstr Aesthet Surg. 2014 Apr 1;67(4):483–8.
24. Wheat JS, Choppin S, Goyal A. Development and assessment of a Microsoft Kinect based system for
imaging the breast in three dimensions. Med Eng Phys. 2014 Jun;36(6):732–8.
25. Versatile design, small size, and light weight | Features | FARO Scanner Freestyle3D | FARO India [Internet]. [cited 2015 Jul 28]. Available from: http://
www.faro.com/en- in/products/3d- documentation/ faro- scanner- freestyle- 3d/features#main
26. Dilek K, Avşar ACA. Anthropometric breast mea­surement: a study of 385 Turkish female students. Aesthetic Surg J Am Soc Aesthetic Plast Surg. 2010;30(1):44–50.
27. Yaffe MJ. Mammographic density. Measurement of mammographic density. Breast Cancer Res BCR. 2008;10(3):209.
28. Schreer I.Dense breast tissue as an important risk fac­tor for breast cancer and implications for early detec­tion. Breast Care. 2009 May;4(2):89–92.
Principles ofRadiotherapy
https://t.me/medicina_free
inBreast Oncoplasty andReconstruction
DayaNandSharma andSupriyaMallick
11
Radiotherapy, by means of double stranded DNA damage (mainly) plays a pivotal role in treatment of most of the solid tumors. Radiation is often employed as denitive treatment option or in sequence with surgery (adjuvant or neo- adjuvant). Modern radiation is delivered either by linear accelerator, which accelerates electrons and pro­duces photon beam and electron beam of varying energies or a brachytherapy machine which uses radioactive sources (Ir tion to a precisely dened lesion. Last two decades witnessed a paradigm shift as breast con­servation surgery (BCS) followed by radiation, coined as breast conservation therapy (BCT), gained popularity and became standard of care in the management if early breast cancer. BCT allowed patients to avoid mastectomy without compromising long term disease control and sur­vival. Initially entire breast used to be irradiated (whole breast irradiation) [1]. Subsequently, it was realized that most of the patients after a con­servation surgery predominantly recur within the same quadrant which introduced the concept of irradiating the quadrant at risk of recurrence and was popularized as partial breast irradiation [2,
3]. Interestingly, after BCS conventional radia-
tion takes nearly 5–7weeks’ time to complete the treatment, which can easily be performed in one
D. N. Sharma (*) · S. Mallick Department of Radiotherapy, All India Institute of Medical Sciences, New Delhi, India
192
or Co60) to deliver radia-
go (intraoperative) or in 1 weeks (interstitial brachytherapy/balloon-based applicators/pho­tons) and hence was termed as accelerated partial breast irradiation (APBI). Professional organiza­tions have laid down suitability criteria for per­forming APBI.All such guidelines come down to the fact that early breast cancer (max size 3cm, N0, no NACT), favorable histology (margin neg­ative, hormone positive, Her2neu- negative) in elderly patients (age 50 or higher) are suitable for APBI and have been established in randomized trials [46]. Over the last two decades, there has been a paradigm shift in surgical management of breast cancer, with increased incorporation of oncoplastic procedures into breast oncologic pro­cedures [7]. Oncoplastic surgery is aimed at excising the tumor with wide surgical margins to deliver better cosmetic outcome. Cosmesis is the most important yard stick to judge a quality of breast cancer surgery after sound oncologic clearance which is mitigated by combining plas­tic surgical approach with oncological surgical approach. This holds immense potential to increase the rate of breast-conserving surgery which is clearly highlighted as American Society of Plastic Surgeons (ASPS) reported a 29% increase in reconstructive surgeries in the year 2018, compared to 2000. Interestingly, nearly 80% of these were implant based, and remaining required both a tissue expander and implant [8]. Radiation technique and understanding of radio­biology have witnessed similar change in the
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2023 S. V. S. Deo (ed.), Breast Oncoplasty and Reconstruction,
https://doi.org/10.1007/978-981-99-5536-7_11
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D. N. Sharma and S. Mallick
mentioned time frame. Modern day radiation delivers precise radiation to the precisely delin­eated target and improves disease control with minimal normal tissue toxicity. In contrast to pre­vious fractionation schedules advent of newer safe protracted treatment course has improved compliance to treatment by several folds. Introduction of motion management during radi­ation has helped to reduce cardiac and lung dose and complications secondary to it. It is obvious that the interplay of oncoplasty and radiation oncology treatment planning and outcomes is complex. Oncoplastic surgeries on the basis of breast size, size, and location of the tumor can be broadly classied as volume displacement and volume- replacement surgery. Transposition of dermo- glandular tissue/ap in the defect is known as volume displacement, whereas in volume- replacement technique autologous tis­sues replace the volume loss.
11.1 Challenges inPatients Undergoing Oncoplasty: Diculty inDelineating Boost Volume
Tumor bed boost was found to reduce local dis­ease recurrence across all age groups [9]. A recent update from the EORTC boost trial high­lighted reduction of local recurrence from 31 to 15% (HR, 0.37; 95% CI, 0.22–0.62; P<0.001) in high-grade tumors in younger than 50 years [10]. It is quite convincing that boost reduces ipsilateral recurrence from 16.4% (no boost) to
12.0% up to 20years without any effect on sur-
vival [10]. Clips placed during surgery, seroma cavity along with the radiological data from mammogram serve as surrogate for delineating the boost volume. Tissue mobilization in onco­plastic surgery poses a challenge in delineating boost volume. In the era of conventional frac­tionation boost was associated with signicant difference inlocal control across all age groups, so patients who opt for conventional fraction­ation are at risk of erroneous boost volume delin­eation. Radiation practice started changing after
Whelan etal. and START group established non­inferior results with 40Gy delivered in 3weeks compared to 50Gy. Recently studies are looking into extreme hypofractionation regimen. However, the hypofractionation trials left the boost to the discretion of the treating physicians and a post-hoc analysis found no signicant impact of boost after hypofractionation radiation [11]. “FAST” trial in UK involving 300 patients tested 30Gy in 5 fractions, 6Gy per fraction over 35 days (5 weeks) Vs 28.5Gy (5.7Gy/Fr) over 35days Vs 50Gy in 25 fractions. Two-year fol­low-up data of the above trial, cosmesis of the breast signicantly affected. The UK-FAST FORWARD and UK IMPORT HIGH are two such trials randomized patients to 40 Gy in 15fractions over 3weeks to 26 and 27 Gy in 5 fractions delivered over a period of 1week. In a recent publication the FAST FORWARD trial published non-inferiority of the 26Gy arm. The importance of boost was further reduced in the FAST-FORWARD trial, but point should be made that the patients included in FAST FORWARD are relatively early risk patients (T3, N0-1). However, this degree of tissue displace­ment in oncoplastic surgery poses a greater chal­lenge to perform accelerated partial breast irradiation (APBI). Efforts are being made to bring homogeneity in practice so that delivery of boost and performing APBI does not compro­mise outcome in the background of oncoplasty. Canadian Locally Advanced Breast Cancer National Consensus Group recently emphasized that surgeon and radiation oncologists should be working in close collaboration and speak “a common language” and there should be homog­enous documentation tumor size, location, defect size, accurate description of the surgical proce­dure. They also emphasized surgical clips should be placed intraoperatively at least one in each of the cavity side walls, which may be helpful in delineating the tumor bed [12]. However, reli­ability of surgical clips to delineate tumor bed is often questioned because of potential chances of clip migration, observer variability [13].
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11.2 Target Denition andDelineation After Oncoplastic Surgery
Accurate target volume delineation is critical for successful implementation of APBI after an oncoplastic surgery. Many guidelines have addressed this issue [14]. According to the Breast Cancer Working Group of the German Society for Radiation Oncology (DEGRO) and GEC ESTRO after a closed cavity surgery, mainstay of target delineation is scar and surgical clips and information from the imaging. The entire area of surgical dissection comes under the term of “whole surgical scar”. Imaging-correlated target volume is delineated with the inputs from preop­erative imaging which typically includes the size, location of tumor. So, the estimated tumor bed comprises the part of whole scar which corrobo­rates with the image correlated target. A safety margin, 20mm minus surgical margin is added to the estimated target volume to create the clinical target volume. In case of brachytherapy based APBI CTV serves as PTV, but in external beam based APBI additional 10mm margin is added to CTV to generate planning target volume. Intraparenchymal placement of clips prior to rotation of glandular tissue is an important pre­requisite for APBI in the setting of oncoplasty.
Additional 10- and 20-mm margin should be added to the clinical target volume for such patients, if being treated with brachytherapy or teletherapy after an oncoplastic surgery (Figs.11.1a, b) [15, 16].
11.2.1 GEC ESTRO Recommendation [15, 16]
1. Perform a CT with marks on the scar.
2. Delineation of clips.
3. Delineation of surgical bed—whole surgical
scar (WS) inside breast.
4. Delineation of ImTV (imaging-correlated tar-
get volume).
5. Delineation of ETB (estimated tumor bed).
6. Delineation of CTV (clinical target volume).
7. Delineation of PTV (planning target
volume).
In case of oncoplastic surgery no recommen­dations can be given but in selected cases of lim­ited rotational aps the CTV can be dened as the sum of the clipped area (CA) and the distance of 20mm minus the smallest surgical free margin (SFM) dened by the pathologist (CTV=CA + (20-SFM)). The PTV is dened as the CTV+10mm.
a b
Fig. 11.1 (a) Representative diagram of target volume delineation in case of APBI. Black dots: Clips, area marked with red-clipped tumor bed, light blue line repre­sents clinical target volume (CTV), which is an expansion by 20mm-surgical free margin, outermost blue line: plan-
ning target volume (PTV) which is an expansion of CTV by 10 mm. (b) Representative image of APBI showing inclusion of clips and other target area covered by pre­scribed dose
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D. N. Sharma and S. Mallick
11.2.2 Optimal Type ofReconstruction intheSetting ofPlanned Adjuvant Radiotherapy
Optimal type of reconstruction is yet to be estab­lished; however, it looks impractical to have a randomized controlled trial to address the issue. Prosthetic based breast implants were in use ini­tially but increasing number of reports high­lighted lesser patents satisfaction and relatively higher complication rate. Autologous reconstruc­tion results in better quality of life as well as fewer complications and failures. Wide range of autologous aps, in particular deep inferior epi­gastric perforator aps are considered superior to transverse rectus abdominal muscle (TRAM) pedicled aps and may be more suitable for PMRT. Other options are latissimus dorsi and muscle-sparing free TRAM aps.
11.2.3 What Is theOptimal Timing ofReconstruction intheSetting ofPlanned Adjuvant Radiotherapy
Adjuvant radiation plays pivotal role in the man­agement of breast cancer after a conservation sur­gery. The early breast cancer trialists’ collaborative group [EBCTCG], in a meta­analysis of 17 randomized trials comprising of 10,801 women treated with or without radiother­apy after a conservative surgery reported that addition of radiation halves the rate at which the disease recurs and reduces the breast cancer death rate by about a sixth [9]. In a subsequently analysis the EBCTCG group highlighted 5.4% reduction in mortality when adjuvant post­mastectomy radiation was added in node positive patients [1]. Earlier small non-randomized trials have evaluated and landed with contradictory results. Huang etal. performed a pooled analysis of 1927 patients and reported that 5-year local recurrence rates in patients treated with RT before chemotherapy (CT) was 6.0% vs. 16.0% in patients treated with CT before RT [17]. Buchholz et al. reported decrease in overall survival and
disease-free survival in patients who received delayed RT (>6months post-surgery) due to a prolonged CT administration [18]. Benchalal et al. reported no increase in local recurrence whether RT was delivered directly after lumpec­tomy, either after the third CT cycle or the sixth CT cycle [19]. However, in multivariate analyses patients with positive margins experienced increased local recurrence rates. In a Cochrane review of published trials Bellon etal. concluded that sequence of administration does not impact on local recurrence or overall survival as soon as RT is administered within 7months after surgery [20]. Most of the above-mentioned studies, reporting impact on local recurrence with late RT delivery in order to administer CT rst, do not provide data on overall survival. In general, no robust evidence suggests any impact on overall survival. RT administration after CT does not result in decreased survival in most of the studies; however, RT should be administered within 7months after surgery.
11.2.4 Managing Margin Positivity
Over the last decade oncological safe margin for breast cancer has evolved, and nowadays if inked margin is free it is considered safe and optimum as any margin positivity leads to higher rate of local recurrence and merits revision. However, in cases of APBI surgical margins should be nega­tive by at least 2mm [21]. A systematic review reported that patients undergoing OPS experi­ence 3–13% close margins and nearly 10% achieve positive margins. The authors concluded that a larger volume of resection does not ensure margin negative surgery always [22]. There are reports of nearly 30% [23] margin positive rate after OPS whereas neither margin positivity rate and local recurrence varied either with conven­tional breast conservation and OPS in other pub­lished data [24, 25]. Amabile et al. reported microcalcications, tumor multifocality, and obesity as predictors of re-excision after OPS.Chen etal. in a metanalysis of all available data found BCS along with OPS safe over BCS alone and the additional OPS decreases re-