AJR Join ARRS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sella, T.
Right arrow Articles by Libson, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sella, T.
Right arrow Articles by Libson, E.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
AJR 2001; 177:857-859
© American Roentgen Ray Society


Value of Chest CT Scans in Routine Ovarian Carcinoma Follow-Up

T. Sella1, E. Rosenbaum2, D. Z. Edelmann2, R. Agid1, A. I. Bloom1 and E. Libson1

1 Department of Radiology, Hadassah University Hospital, P. O. Box 12227, Jerusalem, Israel, 91121.
2 Department of Oncology, Hadassah University Hospital, Jerusalem, Israel, 91121.

Received July 19, 2000; accepted after revision April 11, 2001.

 
Address correspondence to T. Sella.


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The purpose of our study was to examine the role of chest CT scans in routine follow-up of patients who had been treated for ovarian carcinoma.

MATERIALS AND METHODS. The radiologic follow-up of 127 women with metatastic ovarian carcinoma who had undergone surgery and chemotherapy between 1985 and 1996 was reviewed. In reviewing each patient's medical record, we determined whether a chest CT scan had been obtained, and if so, how many had been obtained during the patient's follow-up period. For patients with a chest CT scan, an analysis of the presence of disease in the thorax and its relation to disease in the abdomen and pelvis, as revealed on CT images, was performed.

RESULTS. Of the patients whose cases were examined, 82 (65%) had had at least one chest CT scan obtained, with more than 50% having had three or more scans. Thirty-two (39%) patients had no radiologic evidence of disease. Twenty-eight (34%) showed disease in the abdomen or pelvis but no disease in the chest. Eighteen (22%) had both chest and abdominal or pelvic CT scans that indicated disease. In all of these patients, abdominal or pelvic disease had appeared on scans before spreading to the chest. Four (5%) of the patients had isolated chest disease. The rate of lung metastases from ovarian carcinoma in our series was 6%. In all of these patients, pulmonary metastases were preceded either by abdominal or pelvic disease or by a rise in tumor markers.

CONCLUSION. Pulmonary metastases in ovarian carcinoma are rare and usually preceded by recurrence of carcinoma in the abdomen or pelvis. We suggest that chest CT scanning could be eliminated in the routine follow-up of patients who have been treated for ovarian carcinoma; yet it should be performed for those patients with elevated serum tumor markers but without evidence of abdominal or pelvic disease.


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Ovarian carcinoma is the third most common gynecologic malignancy, affecting approximately one in 70 women [1, 2]. Pleural effusions are reported in 20-25% of patients, whereas parenchymal pulmonary metastases are seen in 7-12% [1, 3]. Review of the English-language literature reveals a consensus regarding the need for routine abdominal and pelvic CT scanning with various protocols as part of the follow-up of this disease [4,5,6,7,8]. However, there are no clear guidelines as to when CT scanning of the chest should be performed.

We undertook a retrospective study to examine the frequency with which chest CT scanning was used as part of the routine follow-up of patients with metastatic ovarian carcinoma. In addition, we assessed the value of chest CT scans by measuring the incidence of thoracic metastasis and its temporal relationship to the appearance of metastatic disease in the abdomen or pelvis.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
A retrospective review was performed of the radiologic and clinical data of 127 women who had been treated for metastatic ovarian carcinoma between 1985 and 1996. Patient age at the time of presentation ranged from 38 to 78 years, with a median age of 54 years. All patients had stage III or IV cancer at the time they were examined. They had been treated by a combination of surgery and chemotherapy at a single institution. Patients were treated and followed up by a single medical team at one oncology day care center. All patients received a similar therapeutic protocol. All were referred for CT as part of their routine follow-up. Patients with clinical symptoms or with previous imaging examinations suggestive of pulmonary disease were excluded from the study. Radiologic and clinical follow-up periods of the patients ranged between 2 and 10 years, with a median period of 3 years.

Data of patients who had at least one chest CT scan, as well as abdominal and pelvic CT scans, available for review were further analyzed to assess the following parameters: the stage of disease during the review period; the number of CT scans obtained of the chest and of the abdomen and pelvis; the presence of metastatic disease and its characterization at each anatomic site; the temporal relationship between the appearance of metastatic disease at different sites; and chronologic correlation of the serum tumor marker (CA-125 and carcinoembryonic antigen) measurements with the presence of metastatic disease visible on CT images. Patients who did not have at least one chest CT scan were excluded from this analysis.

The most recent CT examination in which a chest CT scan had been included was reviewed for each patient, and the status of disease in the chest, abdomen, and pelvis on the date of that examination was assessed. Two independent radiologists reviewed the CT examinations of each patient. Clinical charts relating to the relevant dates were also reviewed.

Thoracic disease was reported as pleural effusion, parenchymal nodules, or both. Abdominal or pelvic disease was defined as the presence of ascites, local recurrence, lymphadenopathy, or omental or hepatic metastases, and was recorded as present or absent. Each patient's data were reviewed and scored as positive or negative for disease at each site according to these criteria. Abdominal and pelvic diseases were grouped together.

After reviewing all data, we categorized the patients into one of four groups: no radiologic evidence of disease in the chest, abdomen, or pelvis (group 1); no radiologic evidence of thoracic disease but evidence of disease in the abdomen or pelvis (group 2); radiologic evidence of both thoracic and abdominal or pelvic disease (group 3); or radiologic evidence of thoracic disease but no evidence of abdominal or pelvic disease (group 4). In a patient with pulmonary metastases present, we reviewed all the chest CT scans dating back to the time before the nodules appeared. We assessed abdominal and pelvic disease and serum tumor markers present in the patient at that time.

Results were calculated as proportions with a 95% confidence interval (CI).


Results
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Of 127 women whose cases we reviewed, 45 (35%) had undergone abdominal and pelvic CT alone, whereas 82 (65%) had had at least one thoracic CT scan as part of their follow-up. In total, more than 300 chest CT scans had been obtained for the patients in our study group. The average number of chest CT examinations per patient was 3.5. Fifty-seven percent of these patients had had three or more chest CT scans obtained, and 44% had had at least four. These data are summarized in Table 1.


View this table:
[in this window]
[in a new window]
 
TABLE 1 Use of Chest CT in Follow-Up of 82 Patients Treated for Ovarian Carcinoma

 

Of the 82 women for whom at least one chest CT scan had been obtained, there were 32 (39%) in group 1, 28 (34%) in group 2, 18 (22%) in group 3, and four (5%) in group 4. Interobserver agreement in assigning a group to a patient was 100% ({kappa} = 1). The incidence of thoracic involvement was 27% (groups 3 and 4). Of these, 16 women had pleural disease (effusion or nodules) alone, two had pulmonary nodules with effusion, and four had pulmonary nodules alone. Only six patients had evidence of lung metastases. One of these was a patient with concomitant ovarian and breast carcinoma whose chest CT scan showed an isolated metastasis. The results of a needle biopsy showed the metastasis to be adenocarcinoma of the breast. Therefore, only five of the 82 patients in our series had pulmonary metastases from ovarian carcinoma. These five patients represent 6% of our patient population (95% CI, 2-13%). These results are summarized in Tables 2 and 3.


View this table:
[in this window]
[in a new window]
 
TABLE 2 Distribution of Disease Arising During CT Follow-Up of 82 Patients Treated for Ovarian Carcinoma

 

View this table:
[in this window]
[in a new window]
 
TABLE 3 Thoracic Involvement Found in Follow-Up CT Scans of 82 Patients Treated for Ovarian Carcinoma

 

All five patients with pulmonary metastases had previous chest CT scans available for review along with the abdominal and pelvic scans obtained on correlating dates. In three of these patients, abdominal or pelvic recurrence had appeared before thoracic disease and had been documented at a previous time when findings of the chest CT scan had been normal. In the two additional patients, pulmonary metastasis was an isolated finding. In both, a rise in serum tumor markers had been noted weeks earlier, at a time when findings of the chest CT scan had been normal. Hence, all cases of pulmonary metastases in our study were preceded either by abdominal or pelvic disease or by a rise in tumor markers.


Discussion
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Ovarian carcinoma is the fourth most common cause of death from cancer in women [1, 2, 9]. The pathways for metastasis of this malignancy have been extensively documented, with the most common site of metastasis reported as being the adjacent pelvic organs [9, 10]. Metastases through lymphatic channels, specifically to paraaortic, external iliac, hypogastric, and inguinal groups of lymph nodes, are well recognized. The peritoneal cavity is another common site of metastasis. Ascites is a frequent feature of the disease in this site. Tumor cells may be transported from the peritoneal cavity via the diaphragmatic lymph channels to the subpleural space and from there to diaphragmatic and paracardiac lymph nodes [2, 10]. Pleural effusions are found in 20-45% of women with ovarian carcinoma [3, 11, 12]. Hematogenic spread is a more rare route of metastasis in ovarian carcinoma. In a review of 255 patients, Dauplat et al. [3] reported hepatic metastases in 9%, parenchymal pulmonary metastases in 7%, subcutaneous nodules in 3.5%, and central neural system metastases in only 2% of patients.

Standard procedure is to follow up patients who have had ovarian carcinoma with periodic CT examinations using one of various protocols. The protocol used at our institution includes an initial abdominal and pelvic CT examination at diagnosis; a baseline CT examination after surgery but before chemotherapy; a CT examination after 3 months if any residual disease was present after surgery; and a CT examination at the end of routine treatment (usually six courses of chemotherapy). If the patient's disease was initially assessed as stage IV, these examinations are followed by a CT examination at 3 months; otherwise, 6-month, 1-year, and 2-year follow-up CT scans are obtained. This protocol, however, does not state when to include chest CT scanning as part of the follow-up. To our knowledge, the literature provides no clear guidelines on when to perform chest CT in patients who have had ovarian carcinoma. A recent study by Dachman et al. [12] is the first attempt to address this issue; the researchers state that the contribution of chest CT to the follow-up of these patients is small.

Our study shows that in our institution, despite the use of a standard protocol, the frequency with which chest CT scanning was performed varied greatly. Thirty-five percent of patients did not have a chest CT scan obtained at any time, whereas 5% of the patients each had eight or more scans obtained. Twenty-three patients had undergone only one chest CT scanning during their follow-up, possibly performed because of clinical concern about the appearance of suspicious symptoms. Of those patients who had been examined using chest CT, most (55%) had had between two and five scans obtained. This wide variation in practice likely reflects a degree of confusion among the referring physicians concerning when to request chest CT scanning for these patients. Therefore, clear guidelines are warranted.

By the end of the follow-up period (average follow-up period, 3.5 years), only 39% of the women in the study group had remained free of disease. Of the 50 patients (61%) with recurrent or metastatic disease, 27% had diseases involving the chest. The majority of these women (82%) had a pleural effusion. Only four patients had isolated pulmonary metastases, just 8% of all those with recurring disease, with an upper 95% confidence value of 19%. The remaining 46 patients had experienced either coinciding abdominal or pelvic disease or pleural disease, all of which could have been detected on a standard abdominal CT examination. A recent study of thoracic involvement in patients with metastatic ovarian carcinoma found that 77.8% of such disease was located in the lower thorax [12].

Because of the retrospective nature of our study, some bias toward patients with pulmonary disease may exist. Even so, only five patients in our study group had pulmonary metastases from ovarian carcinoma. This finding, together with that cited from the literature, suggests that parenchymal pulmonary metastases are rare in patients who have been treated for ovarian carcinoma. Furthermore, in the patients in our study, all cases of pulmonary metastases were preceded either by recurrent abdominal or pelvic disease that was detectable on CT images or by a rise in serum tumor markers. This finding correlates with those of Dachman et al. [12] who found progression of chest disease without previous progression of abdominal or pelvic disease in the findings of only 2.7% of CT scans of 40 patients with metastatic ovarian carcinoma. The coexistence of pulmonary metastases with recurrent or metastatic abdominal or pelvic disease does not necessitate a change in therapeutic strategy.

On the basis of our results, we suggest that routine chest CT scanning may be eliminated in the follow-up of patients who have been treated for ovarian carcinoma. This practice adds significant cost and exposes the patient to unnecessary discomfort and radiation. Thoracic CT scanning is definitely indicated in the patients with an elevation in serum tumor markers but without evidence of recurrent or metastatic abdominal or pelvic disease. A patient who experiences onset of new respiratory symptoms may also need a chest CT scan so that any pulmonary metastases or other possible thoracic diseases may be diagnosed.

In conclusion, the most common thoracic involvement in patients who have been treated for ovarian carcinoma is pleural effusion, which can easily be revealed on abdominal CT images performed according to standard protocols. Pulmonary metastases are rare and usually are preceded by recurrence of disease in the abdomen or pelvis. Therefore, we suggest that chest CT scanning may be eliminated from the routine follow-up protocol of patients who have had ovarian carcinoma and should be reserved for those patients with elevated serum tumor markers but without evidence of abdominal or pelvic disease. To establish the efficacy of our proposed change, a prospective study using a standardized protocol is warranted.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Kerr VE, Cadman E. Pulmonary metastases in ovarian cancer. Cancer 1985;56:1209 -1213[Medline]
  2. Holloway BJ, Gore ME, A'Hern RP, et al. The significance of paracardiac lymph node enlargement in ovarian cancer. Clin Radiol 1997;52:692 -697[Medline]
  3. Dauplat J, Hacker NF, Nieberg RK, et al. Distant metastases in epithelial ovarian carcinoma. Cancer 1987;60:1561 -1566[Medline]
  4. Kalovidouris A, Gouliamos A, Pontifex G, et al. Computed tomography of ovarian carcinoma. Acta Radiol Diagn (Stockh) 1984;25:203 -208[Medline]
  5. Ferrozzi F, Bova D, De Chiara F, et al. Thin-section CT follow-up of metastatic ovarian carcinoma correlation with levels of CA-125 marker and clinical history. Clin Imag 1998;22:364 -370
  6. Ahmed FY, Wiltshaw E, A'Hern RP, et al. Natural history and prognosis of untreated stage I epithelial ovarian carcinoma. J Clin Oncol 1996;14:2968 -2975[Abstract]
  7. Prayer L, Kainz C, Kramer J, et al. CT and MR accuracy in the detection of tumor recurrence in patients treated for ovarian cancer. J Comp Assist Tomogr 1993;17:626 -632[Medline]
  8. Whitley N, Brenner D, Francis A, et al. Use of the computed tomographic whole body scanner to stage and follow patients with advanced ovarian carcinoma. Invest Radiol 1981;16:479 -486[Medline]
  9. Young RC, Fuks Z, Hoskins WJ. Cancer of the ovary. In: DeVita VT Jr, Hellman S, Rosenberg SA, eds. Cancer principles and practice of oncology, 3rd ed. Philadelphia: Lippincott, 1989: 1162-1191
  10. Fuks Z, Bagshaw MA. The rationale for curative radiotherapy for ovarian carcinoma. Int J Radiat Oncol Biol Phys 1975;1:21 -32[Medline]
  11. Johnston WW. The malignant pleural effusion. Cancer 1985;56:905 -909[Medline]
  12. Dachman AH, Visweswaran A, Battula R, Jameel S, Waggoner SE. Role of chest CT in the follow-up of ovarian adenocarcinoma. AJR 2001;176:701 -705[Abstract/Free Full Text]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?



This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sella, T.
Right arrow Articles by Libson, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sella, T.
Right arrow Articles by Libson, E.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS