Micropapillary bladder cancer: a review of Léon Bérard Cancer Center experience

Micropapillary bladder carcinoma is a rare variant of urothelial bladder cancer recently described by Amin et al [1], and accounting for 0,7 to 2,2% of all urothelial tumors. It is associated with a rapid growth rate and an advanced stage at presentation [1, 2]. We retrospectively analyzed 11 consecutive cases of muscle-invasive or metastatic micropapillary bladder cancer treated at the Léon Bérard cancer center between 1994 and 2007 in order to better define the behaviour of this aggressive disease.

We retrospectively searched the files of all patients with muscle-invasive or metastatic micropapillary bladder carcinoma treated at the Léon Bérard cancer center between 1994 and 2007. Patients were considered to have micropapillary disease if the pathology report revealed any micropapillary component (MPC) in their tumor. Patient medical records were analyzed for demographic characteristics, clinical stage and outcome. Radiology, pathology and surgical reports were reviewed to determine the pathological staging at the time of cystectomy using the 1997 TNM classification for genitourinary tumors [3]. Chemotherapy regimens, radiotherapy doses and surgical modality were also recorded. Overall survival was calculated from the date of diagnosis to the date of death or the date of last follow-up. Estimation of survival curves was performed using the Kaplan-Meier technique.

Carcinoma with MPC was first described in 1982 as a variant of endometrial carcinoma initially designed as papillary serous carcinoma of the uterus [4]. Later, this subtype was depicted in thyroid [5], breast [6], urinary tract [1] and lung cancers [7].

Amin et al were the first to describe this entity in urothelial carcinoma, in 1994. They identified two distinct morphologic appearances. On the surface MPC are characterized by small papillary tufts and slender, delicate processes, often with a central fibrovascular core while in the invasive part, the cells form small tight nests or balls often seen within retracted connective tissue spaces [1]. Associated typical urothelial carcinoma is usually high grade as was shown in our series. Immunohistochemical profile typically shows CK7+/CK20+(CA125+/-) suggesting that it is a form of glandular differentiation in urothelial carcinoma [8, 9].

Described less than 15 years ago, micropapillary bladder cancer is likely underreported. In our institution, only 1 patient was diagnosed before year 2000 while the other 10 patients were identified between 2001 and 2007 mainly after 2004 (8 cases). This suggests that the reported frequency of micropapillary bladder cancer might increase in the future as pathologists and oncologists become more aware of its description and particular clinical behavior.

To date, there are no prospective trials in micropapillary bladder cancer. Our retrospective study is the third largest clinical series of muscle invasive and metastatic bladder cancer reported in the literature after Kamat et al who described 56 consecutive cases [10] and Johansson et a l who reported 17 consecutive cases [2]. The other relatively large series are clinicopathological studies with no correlation between treatment and outcome [1, 8, 11].

The presence of MPC in urothelial carcinoma was found to be associated with an advanced stage of disease at the time of presentation and an aggressive clinical course [8, 9, 11, 12]. In 2004, Samaratunga et al. [8] reported 20 cases of micropapillary bladder cancer and correlated the pathological stage and prognosis with the extent and extension of the micropapillary component on the pathology specimen. In patients with superficial bladder cancer, intravesical BCG was shown to be ineffective and the authors concluded that the optimal treatment strategy for non-invasive bladder cancer with micropapillary components should be a radical cystectomy [13]. The same authors stated in another study that in muscle invasive surgically resectable disease, radical cystectomy should be performed precociously. In this paper, the incidence of pathologic upstaging was 52.7% and the incidence of occult lymph node disease detected at the time of cystectomy was 27.3%. Moreover patients undergoing neoadjuvant chemotherapy were found to have a non-organ-confined disease (≥ T3) in 68% of cases compared to patients treated with upfront surgery (34%) (p = 0,0157). There was no survival benefit from the addition of neoadjuvant chemotherapy and the authors recommended no such approach especially in the absence of lymphovascular invasion [10]. Moreover, in this study, of the 15 patients with lymph node positive disease, 11 received adjuvant chemotherapy after radical cystectomy, and only 5 were alive at the time of last follow-up (follow-up time ranging from 29 to 42 months). This tends to show the chemoresistant characters of micropapillary bladder cancer. In fact, in other organ sites, micropapillary carcinoma appears to be less responsive to chemotherapy. For example, a retrospective study evaluated the pattern of chemoresistance in invasive micropapillary/low grade serous ovarian carcinoma and high grade serous ovarian carcinoma. Authors concluded that patients with recurrent invasive micropapillary/low grade serous ovarian carcinoma were more likely to manifest drug resistance to standart chemotherapy agents (platinum and paclitaxel) [14].

The present study showed occurrence of the disease in relatively young patients (median age was 60 years) and an associated poor prognosis. Patients who received multimodal treatment had a median disease free survival of 11 months and an overall survival of 21 months. All 5 patients with node positive disease who received surgery followed by adjuvant MVAC regimen relapsed within a median follow up of 20,2 months. This is in sharp contrast with other studies that used same treatment modalities for node positive resected urothelial carcinoma [15–18]. In the study by Stokle et al, only 3 among 11 patients relapsed after a median follow-up period of 13.5 months [15]. In the study by Freiha et al, 10 patients out of 18 relapsed after a median follow-up of 62 months [16]. This further emphasizes on the aggressive character and chemoresistance of this variant of urothelial carcinoma.

Micropapillary bladder cancer is very likely an underreported variant of urothelial carcinoma. It is associated with a poor prognosis. The low incidence of this variant renders the conduct of randomized trials rather impossible and drawing clear guidelines for its management is subsequently difficult. Nevertheless, our series suggests that adjuvant chemotherapy might have a questionable efficacy especially in node positive disease, and the optimal treatment modality remains to define.