Primary pulmonary choriocarcinoma

A 35 year old woman complaining of severe right sided chest pain was admitted to our hospital. The patient had three normal term deliveries in the past 15 years and three spontaneous abortions in the past year. The chest radiograph showed a round opacity in the right lungs. A computed tomographic scan (CT) of the chest revealed the presence of 6.4 × 5.4 × 5.9 cm pulmonary mass in the right lower lobe (Figure 1A). Transthoracic needle biopsy was performed and diagnosis of poorly differentiated giant cell carcinoma (GCC) was made. To exclude additional masses FDG-PET study was performed (Figure 1B). FDG accumulation in the pulmonary mass was low, maximum standardized uptake value (SUVmax) was 2.7, and only in the periphery of the mass. No other abnormal accumulation was detected in whole body including pelvic cavity. During hospitalization the patient’s condition progresively worsened with depleting levels of hematocrit, hemoglobin and platelets. Urgent right sided bilobectomy with pericard excision was performed. Histopathologic workup of excised tumour showed poorly differentiated carcinoma with trophoblast differentiation, most consistent with choriocarcinoma. Excised nodes showed no tumour infiltration.

Four weeks after surgery the patient was admitted to our hospital to start chemotherapeutical treatment. In these four weeks the patient had two episodes of epileptical seizures. CT and MRI of the head showed 1 cm intracerebral metastasis with surrounding edema (Figure 1C).

The patient began EMA-CO regimen chemotherapy with high dosage methotrexate. At the start of the chemotherapy plasma hCG levels were 169396 IU/L, on eighth day fell to 20883 IU/L and after three months (4 cycles of chemotherapy) the plasma hCG levels fell within normal range. Patient underwent stereotactic radiotherapy of cerebral metastasis with dose 1 × 25 Gy after the fourth cycle and afterwards received two additional cycles of EMA-CO regimen with standard dose of metotrexate. To completely rule out the origin of the tumour in reproductive tract the vaginal total hysterectomy with bilateral salpingoectomy was performed after 6 cycles of chemotherapy and histopathological examination was negative.

According to FIGO clinical and prognostic staging patient had stage IV disease with high-risk score.¹² Brain MRI was performed 7 months after stereotactic radiotherapy and showed 3 mm residual mass with no surrounding edema. Patient is on regular follow-up and is still on therapy with levetiracetam and dalteparin without evidence of relapse at 12 months following surgery.

The patient was treated according to the Helsinki Declaration. She gave a written informed consent before treatment to use her clinical data for research.

We searched the literature with a PubMed search to establish characteristics of PPC using criteria described in Patients and methods. A review of the literature in English revealed 54 cases with previous report of primary choriocarcinoma originating in the lung.^{1-10,13-15,17-44} The patient described in the present paper was analysed with other 54 reported cases. The profiles of the patients are summarized in Table 1; 17 men and 38 women were included with a median age of 34 years (range 0.3 to 77). At the time of discovery 47 patients (85%) produced symptoms, including persistent cough (40%), dyspnea (31%), hemoptysis (25%) and chest pain (20%). At presentation 8 tumours were asymptomatic. A few of the women have presented with hormonal problems such as amenorrhea or vaginal bleeding. In men, signs of feminisation such as gynecomastia have been observed but are uncommon.

We analysed the relationship between gender and other clinicopathological features in patients with PPC (Table 2). Men were older than women (p = 0.000). Men had the history of smoking more often than women (p = 0.000). No statistically significant difference between genders was observed for location, size, presence of metastases, history of haemoptysis or treatment.

Only 47 cases (16 men and 31 women) reported treatment outcome. The median survival time was 8 months. The review of these 47 cases showed 1-, 2-, and 5- year survival rates of 61%, 57% and 49%, respectively. Important difference (p = 0.004) in survival time between genders was observed with women showing 1-, 2-, and 5- year survival rates of 77%, 77% and 64% while men showed 1-, 2-, and 5- year survival rates of 31%, 21% and 21%, respectively (Figure 2A).

In Table 3 univariate analysis is shown. Younger patients (< 40 years) survived longer than older patients (≥40 years), (p = 0.009). Patients with smaller tumours (< 5cm) survived longer than patients with larger tumours (≥ 5cm), (p = 0.000). Survival of patients without metastases at presentation was longer than for patients with metastases (p = 0.000). Patients without the history of smoking survived longer than patients with the history of smoking (p = 0.001). The women were further divided into two groups according to the history of gestational events (such as abortion, pregnancy or hydatiform mole) within the time period of less than 7 years prior the admission. Women with the history of gestational event (n = 14) had better survival outcome than women without the history of gestational event (n = 17), the difference was statistically significant (p = 0.040), (Figure 2B). Patients treated with combination of surgery plus chemotherapy survived longer than those treated with optimal supportive care or either chemotherapy or surgery alone (p = 0.001). Patients treated with chemotherapy only survived less than the patients treated with surgery only or combination of chemotherapy and surgery (p = 0.016). Patients treated with combination of surgery and chemotherapy survived longer than patients without combination of surgery and chemotherapy (p = 0.010). Treatment with surgery demonstrated no significant prognostic influence.

As shown in Table 4, multivariate analysis of prognostic factors using the Cox proportional hazards model showed that the treatment combining surgery with chemotherapy had independent prognostic significance (p = 0.007). Furthermore, the size of the lesion showed an independent prognostic significance (p = 0.008).

PPC occurs in women in younger ages than in men (33 vs. 60 median age), an observation already described by Umemori et al.⁸ Therefore, it can be derived that PPC in women is more likely to occur in the reproductive period. Furthermore, there are more reported cases with women than men. Statistically significant difference in survival time between genders was observed with women showing better outcome. We further divided women in two groups due to the history of the gestational event within the time period of less than 7 years prior the admission. We chose the cut off of 7 years conservatively on the basis of three published cases with genetical examination.^6,7 In the paper by Maesta et al. they present two patients with gestational event within 4 years prior to PPC diagnosis and in both cases they proved it to be of gestational origin.⁶ In the paper by Vegh et al. the patient had the last gestational event 7 years prior to admission and with fluorescence in situ hybridization they excluded gestational origin, no paternal chromosome was found in tissue examinated.⁷ Based on this assumption we considered that women with the history of gestational event less than 7 years had better survival outcome than women without such history of gestational event.

Looking at aforementioned gender differencies, PPC seems to be of different etiology in men. Furthermore, we showed that men have a history of smoking more often than women. To support the theory of dedifferentiation four cases of PPC have been reported with co-existent pulmonary carcinoma.^5,10,13,14 All were male patients, in three cases PPC was sinchronous and found at autopsy, in one case the PPC was metachronous arising 6 years after diagnosis of squamous carcinoma. Problematically primary pulmonary carcinomas can produce hCG. Ikura et al. reported more intense expression of hCG in PPC than in hCG producing GCC.¹⁴ Although this finding seemed to reflect the level of serum hCG the cut off point seemed to be ambigous.¹⁵ Because of the rarity and clinicopathological similarity of PPC and hCG producing GCC the criteria for distinguishing them are unclear and the diagnosis is very difficult.¹⁴

The survival data should be handled cautiously because of the possibility that mostly patients with good survival were reported in the literature and the rest were neglected. Nevertheless PPC is notorious for having a poor prognosis, however, the present review shows 1-, 2-, and 5- year survival rates of 61%, 57% and 49%, which is reasonably good. Furthermore, if only female patients are observed the survival rates are even higher. Patients having smaller size tumour and being without metastases at diagnosis have higher survival rate, thus early diagnosis with optimal management is important. The outcome is still worrying but in comparison with the review article from the year 2004 by Umemori et al. where they reported 1-, 2-, and 5- year survival rates of 41%, 34%, 34% the outcome results are more promising. We noticed that the early reports of PPC had poorer outcome than the ones nowadays and that chemotherapeutical treatment was rarely used in the cases prior to year 1994 but if chemotherapy was used it was single modality therapy. The evolvement of chemotherapeutical treatment and better supportive therapy could influence the better outcomes seen in the present review, but we could not attribute the difference in survival rates to the specific factor due to the rarity and nonexistence of therapeutic guidelines.

In order of finding out any relationship between treatment and survival the univariate and multivariate analysis of prognostic factors was carried out. Univariate analysis showed that treatment with chemotherapy only is not good choice of treatment however significant prognostic influence for combined treatment with surgery and chemotherapy was found. Furthermore, multivariate analysis of prognostic factors revealed that combined treatment with surgery and chemotherapy had independent prognostic significance. These findings are in concordance with already known facts that PPC is very aggressive disease, not just locally, but also by early spread to other organs.⁴ Therefore, combined modality treatment (surgery and chemotherapy) represents best possible way to improve survival. Of course patients have to be fit enough for such aggressive treatment. No reports of extended survival were found in patients who underwent complete resection without chemotherapy.