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Journal of Contemporary Brachytherapy
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Case report

Complete response in a patient with gynecological hidradenocarcinoma treated with exclusive external beam radiotherapy and brachytherapy: a case report

Flavio Giannelli
,
Ilaria Chiola
,
Liliana Belgioia
,
Stefania Garelli
,
Alice Pastorino
,
Michela Marcenaro
,
Serafina Mammoliti
,
Sergio Costantini
,
Nicolò Bizzarri
,
Valerio Vellone
,
Salvina Barra
,
Renzo Corvò

J Contemp Brachytherapy 2017; 9, 6: 572–578
Online publish date: 2017/12/30
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Purpose

Hidradenocarcinoma (HC) is a rare malignant adnexal tumor, it represents approximately 6% of malignant eccrine cancers and its incidence is about 0.001% of all malignant tumors [1]. Hidradenocarcinoma affects mainly females from the fifth to the seventh decade of life [2]. The head and neck are the most common sites of HC, but occasionally it can occur in other locations [3,4]. Despite the fact that HC has an aggressive behavior, it may remain asymptomatic for some time. The first site of meta­static spread is lymph nodes [5]. Hidradenocarcinoma arising from the vulva is an extremely rare condition and so far, only few cases have been reported [6]. Here, we report the case of a woman with vulvar localization of HC who was referred to our Institution and to be considered for radical radiotherapy after previous unsuccessful chemotherapy.

Case report

In October 2015, a 60-years-old Caucasian woman, with no relevant past medical history except for removal of a benign breast nodule, was referred to our department reporting few episodes of vaginal bleeding, which started 6 months earlier. Gynecological examination revealed the presence of a circumferential vaginal mass arising from the introitus, and involving the lower and mid third of vagina. Rectal examination was suspicious for parametrial infiltration. Magnetic resonance imaging (MRI) revealed abnormal circumferential thickening of the vagina, mainly located on the anterior and left vaginal wall, with signs of infiltration of the left elevator ani-muscle and of the postero-basal bladder wall. In addition, there was a 28 × 25 mm2 solid lesion in the uterine cervix, strongly suspicious for a malignancy with sign of bilateral parametrial infiltration. The lesion extended to the uterine cavity and a 3.5 x 2 cm2 right lymphoadenomegaly was noted (Figure 1A-B). The subsequent 18-fluorodeoxyglucose positron emission tomography (18-FDG PET/CT) confirmed MRI findings with pathologic uptake of uterus-vagina (standardized uptake value [SUV] 7), rectum (SUV 10.3), and right inguinal nodes (SUV 6.1). A colonoscopy with biopsy was performed to evaluate if there was a rectal involvement, and it revealed an adenoma at the level of rectosigmoid junction. Tumor markers were not elevated (squamous cell carcinoma antigen: SCC = 0.80, and cancer antigen 125 [CA-125] = 23.40). Computed tomography (CT) scan of chest and abdomen showed no evidence of distant metastasis. The patient underwent incisional biopsy of the vaginal introitus. Histological examination of the surgical specimen revealed a lobulated infiltrating neoplasm (Figure 2A) constituted by different cell populations. The first constituted by columnar apocrine cells organized in irregular cystic, tubular, and papillary structures diffusely intermingled with squamous and myoepithelial cells. All the populations showed a mild degree of atypia, pleomorphism, and scattered mitotic figures. The neoplastic epithelial-stromal interface showed significant desmoplasia strongly suggesting pushing infiltration (Figure 2B). The multiphasic nature of the observed neoplasm was confirmed by immunohistochemistry testing, showing a strong positivity of citokeratin 7 in the apocrine component (Figure 2C), no staining for citokeratin 20 in all the components (Figure 2D), a strong positivity for p63 and citokeratin 34E12 in the squamous and myoepithelial components (Figure 2E). Interestingly, we observed a strong and diffuse positivity for p16 (Figure 2F) in the squamous component, similar to that observed in human papilloma virus (HPV)-related squamous dysplasia of cervix and vulva, while the apocrine component showed only scattered positivity. No stain for p53 was observed. On the base of morphology and immu­nophenotyping, and according to the clinical staging, a final diagnosis of HC was made.
A further biopsy at cervical level was required, but it was not feasible due to the stenosis induced by the disease. A radical surgery, as a first treatment option was considered not possible due to the disease extension, and after multidisciplinary team discussion, the patient was treated with capecitabine-based chemotherapy (CT) from March to September 2015. After six cycles, stable disease was confirmed by clinical examination and radiological investigations. Revaluation MRI showed solid tissue to the medial rectum 10 cm from anal margin. 18-FDG PET/CT confirmed MRI detection, with pathologic uptake in uterus-vagina (SUV 5.8), rectum (SUV 15), and right inguinal nodes (SUV 6.9). A second colonoscopy was performed and the previously detected adenoma was endoscopically resected. The patient was considered non-respondent to chemotherapy and was referred for exclusive radiation treatment.

Radiotherapy technique

Radiotherapy treatment was divided in two phases: a first phase of external beam radiotherapy (EBRT) delivered by helical tomotherapy with simultaneous integrated boost (SIB), followed by a second brachytherapy phase. A simulation CT scan with 2.5 mm slices was co-registered with post chemotherapy MRI, and 18-FDG PET/CT in order to delineate the target volumes and organs at risk (OAR). The following volumes were identified: gross tumor volume (GTV), clinical target volume (CTV) whole pelvis (CTV1) including uterus, vagina, anus elevator muscle, and external and internal iliac, obturators inguinal nodes, and simultaneous integrated boosts (SIB) considering the area of metabolic uptake at 18-FDG PET/CT. SIB1 included fundus of uterus and right inguinal node, SIB2 lower/middle third of vagina, paraurethral region and right inguinal lymph nodes. The planning target volume (PTV) were defined adding 5 mm margin to CTV. Prescription doses were 50.4 Gy in 28 fractions (5 fractions per week) to PTV1, 60.2 Gy in 28 fractions to SIB1, and 58.8 Gy in 28 fractions to SIB2 (Table 1). This radiotherapy schedule was chosen taking into account subsequent brachytherapy treatment contribution.
Hi-Art Planning Station with Field Width 2.5 cm, Modulation Factor 2.7 and Pitch 0.287 was used for EBRT. Duration of treatment was 8.3 min. Before each treatment fraction, a MegaVoltage CT scan was performed for patient positioning. Image matching was done daily with an automatic bone algorithm supervised by experienced medical staff. The following goals were planned: at least 95% of the volume was covered by 95% of the dose, at least 99% of the volume was covered by 90% of the dose for all PTVs, and maximum dose for PTVSIB1 and for PTVSIB2 was 62.25 Gy and 61.60 Gy, respectively.
The main organs at risk (OAR) were: bladder, urethra, small bowel, large bowel, head and neck bilateral femoral, and pelvic bones. At the end of EBRT, the patient underwent clinical and radiological assessment with partial response. External beam radiotherapy was followed by 3D image-guided brachytherapy (3D IGBT) high-dose-rate (HDR) (MicroSelectron HDR, Elekta, Sweden). Each brachytherapy session was performed under general anesthesia and ultrasound guidance to evaluate the appropriate positioning of the Fletcher CT/MRI applicator in the uterine cavity. After each insertion of the tandem and ovoid, the patient underwent 3T T2-weigthed MRI for the contouring of GTV, high-risk CTV (HR-CTV), and intermediate risk CTV (IR-CTV) [7]. Oncentra Masterplan TCS version 3.1.5 (Elekta, Stockholm, Sweden) was used for dose calculation with advanced collapsed cone engine (ACE) algorithm. This dose calculation algorithm for brachytherapy is based on the TG-186 recommendations, as published by the AAPM workgroup in 2012. The dose volume histograms (DVH) related to HR-CTV, IR-CTV, and organs at risk (OAR) were evaluated, taking into account in particular D90 for the CTV and D2cc, D1cc, D0,1cc for OAR (rectum, sigma, bowel, bladder, and urethral). Restaging MRI following EBRT showed a moderate reduction of vaginal tissue with right paraurethral extension, and relevant reduction of cervical and fundus of uterus disease (Figure 3). Therefore, it was decided to identify two volumes called HR (high risk), which included: HR-CTV1, including cervix, fundus of uterus, and upper third of vagina, HR-CTV2 including middle third of vagina, and paraurethral region. The doses prescribed were 28 Gy in 4 fractions to HR-CTV1 (Figure 4), 22 Gy in 4 fractions to HR-CTV2 (Figure 5). The total dose of EBRT + IGBT was calculated with a dose equivalent of 2 Gy (EQD2), assuming / = 10 for T and / = 3 for the OAR, with the objective of D90 HR-CTV ≥ 84 Gy10, D2cc ≤ 70-75 Gy3, ≤ 90 Gy3, and ≤ 60 Gy3 for rectum, bladder, and bowel, respectively, D0,1cc ≤ 80-85 Gy3 for urethra. D90 was 91.9 Gy in the HR-CTV1 and 86.0 Gy in the HR-CTV2, D2cc = 67.4 Gy, D1cc = 71.2 Gy, D0,1cc = 79.3 Gy for rectum, D2cc = 75.5 Gy, D1cc = 80 Gy, D0,1cc = 91.1 Gy for bladder, D2cc = 59.8 Gy, D1cc = 62.8 Gy, D0,1cc = 69.5 Gy for sigmoid, D2cc = 59.8 Gy, D1cc = 62.8 Gy, D0,1cc = 69.5 Gy for bowels, and D0,1cc = 75.4 Gy for urethra. Patient reported a grade 2 radiation-correlated cystitis (according to CTCAE v. 4.0) and an episode of urinary retention grade 2 (CTCAE v. 4.0), which resolved completely with clinical treatment [8].

Follow-up

The first radiological follow-up was performed 3 months after the end of treatment with a gynecological examination, MRI, and CT scans, and tumor markers evaluation with significant dimensional reduction but persistent tumor (Figure 6). One month later the subsequent PET/CT showed a complete metabolic response, and the subsequent MRI performed at 6 months from the end of therapy confirmed this datum (Figure 7). At date, there were no relevant late side effects. The patient did not present any recurrence until February 2017. One year after the end of radiotherapy, a CT scan revealed a right lung nodule with avid 18-FDG uptake at PET/CT. The patient underwent stereotactic body irradiation (SBRT) (48 Gy in 4 fractions). The subsequent PET/CT performed at 3 months showed a reduced 18-FDG uptake of the treated nodule and the appearance of a contralateral lung nodule. At date, the patient was planned for another SBRT, and then she will be re-evaluated by medical oncologist for systemic therapy.

Discussion

Hidradenocarcinoma of the vulva is a rare tumor with aggressive development and high-risk of distant metastases with five-year post-surgical survival rate smaller than 30% [9]. It arises from ano-genital mammary gland-like tissue, mainly de novo, and in rare cases, it may stem from a pre-existing hidradenoma [9]. The main location is the head and neck region, rarely on the trunk, abdomen, fingers, or scalp. Our patient presented a vulvar origin, which is exceptionally rare site; a review of the current literature reveals only 7 cases of HC arising from a vulva site. The diagnosis is based on histological and immunohistochemical analysis to differentiated HC from several benign (like hemangiomas, lipomas) and malignant tumors [5]. As HC is a rare disease, to date, there is no clear consensus about its treatment. However, surgery remains the cornerstone of treatment and negative margins of resection are extremely important with some data suggesting that at least a 3 cm margin is required [10,11]. Obviously, surgery depends on the stage of the tumor. In our case, the disease was locally advanced with positive inguinal node and adjacent organs involvement, thus these features did not allow radical surgery even with an extremely radical operation. We started chemotherapy as a treatment to our patients with neoadjuvant intent, but with no benefit. Data regarding chemotherapy in HC are not clear and benefits have not been demonstrated, however normally, the first line treatment is based on 5-fluorouracil and capecitabine, as the molecular pattern of HC is similar to colon and breast cancers [4,12,13]. Radiotherapy is not the first choice of treatment, usually being proposed when surgery is not indicated [12,14]. Radiotherapy has been used in several cases of HC with conflicting results. If the aim of radiation therapy is to achieve a complete response, it is important to weight the balance of administering the highest dose possible with an acceptable morbidity; for this reason, some data recommend doses between 50-70 Gy [12,14]. As our patient was deemed not operable and demonstrated poor response to chemotherapy, we decided to approach her with a high-dose radiation treatment with intensity modulated-RT and subsequent brachytherapy.
Brachytherapy is an optimal treatment option for primary and recurrent carcinomas of the vagina and of vulva; numerous brachytherapy techniques have been developed (as single channel cylinder, interstitial brachytherapy or multichannel cylinder), the decision of which brachytherapy technique to employ is influenced by multiple factors (tumor location, extent of disease, response to EBRT).
In our case, probably a better coverage of paraurethral disease could be obtained with interstitial brachytherapy, but in our institute we did not implement this technique, and the patient refused to move far away from her residence [15,16].
Our patient underwent a tailored treatment that allowed us to obtain a complete response, although the wide extension of the disease at diagnosis, with acceptable short term toxicity and, at date, also long term toxicity. Despite this excellent outcome, HC remains an aggressive disease with poor prognosis (our patient developed lung metastasis).

Conclusions

The present case report shows that EBRT and bra­chy­therapy are feasible options in the treatment of HC, with possibility to obtain local control and acceptable tolerance. Despite this, a longer follow-up is necessary to evaluate the risk of late toxicity that could appear also after a long time from RT.

Disclosure

Authors report no conflict of interest.

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Copyright: © 2017 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
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