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MULTIPLE CANCERS: ORIGINAL ARTICLE
Year : 2016  |  Volume : 5  |  Issue : 1  |  Page : 29-32

Multiple primary cancers: An enigma


1 Department of Surgical Oncology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India
2 Department of Pathology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India
3 Department of Radiology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India

Date of Web Publication5-Apr-2016

Correspondence Address:
Amitabh Jena
Department of Surgical Oncology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2278-330X.179698

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  Abstract 

Background: Incidence of multiple primary cancers though uncommon, is being frequently reported now-a-days owing to better diagnostic techniques, the prolonged life span and the increased incidence of long-term survival of cancer patients. Materials and Methods: This is a retrospective study. Cases of multiple malignancies diagnosed histopathologically were retrieved from the archives of department of surgical oncology. Clinical data were obtained from the medical records. They were categorized as synchronous malignancies if the interval between them was less or equal to 6 months and metachronous, if the interval was more than 6 months. Results: A total of 13 cases were encountered in the 5 year study period. Out of them two were in the metachronous category and the rest were synchronous as the 2nd malignancy was detected mostly during clinical evaluation of the patients for the primary malignancy. There was female predominance with age range being 43-68 years. Majority of the cases were in the 7th decade. The most common organ involved was breast, followed by cervix. Apart from bilateral breast malignancies, there were combinations like breast with uterine endometrial carcinoma, cervical carcinoma and even papillary thyroid carcinoma. Conclusion: Detection of multiple primary malignancies is becoming increasingly common in day-to-day practice. Greater awareness of this is required among both cancer patients and their treating clinicians.

Keywords: Dual malignancies, metachronous malignancy, multiple primary cancers, synchronous malignancy


How to cite this article:
Jena A, Patnayak R, Lakshmi AY, Manilal B, Reddy MK. Multiple primary cancers: An enigma. South Asian J Cancer 2016;5:29-32

How to cite this URL:
Jena A, Patnayak R, Lakshmi AY, Manilal B, Reddy MK. Multiple primary cancers: An enigma. South Asian J Cancer [serial online] 2016 [cited 2019 Sep 20];5:29-32. Available from: http://journal.sajc.org/text.asp?2016/5/1/29/179698


  Introduction Top


Multiple primary cancers are usually defined as primary malignant tumors of different histological origins in one person. Recently, there has been an increase in the number of patients diagnosed with multiple primary cancers. This trend can be attributed to improved diagnostic techniques, prolonged life span and the increased incidence of long-term survival of patients with malignancy. Most multiple primary cancers are double primary cancers.[1],[2]

Definitions and classifications for multiple primary cancers and multi-centric cancers, proposed by Moertel way back in 1977 hold true even today.[2],[3] Accordingly, group I includes, multiple primary cancers occurring in organs with the same histology, group II includes multiple primary cancers that originate from different tissues and group III consists of cancers from different tissues and organs that concurrently exist with group I cancers, and they form multiple primary cancer of three or more cancers. Group I is further subdivided into group A, which includes cancers that occur in the same tissue and organ, group B, which includes cancers that are from the same tissue and different organs, and group C, which includes cancers that occur in bilateral organs. Multiple primary cancers are again classified as synchronous and metachronous. Those malignancies that are observed at the same time or within 6 months are termed as synchronous multiple primary cancers, and those cancers that develop at more than a 6-month interval are termed as metachronous multiple primary cancers.[4] On the other hand, many studies have defined 1 year as the dividing time of these two types of multiple cancers.[5]

In Indian literature, scant data is available regarding multiple primaries, most of them being case reports, including two from our institute.[6],[7],[8],[9],[10],[11],[12],[13] In this retrospective study, we have analyzed the multiple cancers encountered in the department of surgical oncology of a single institute over a 5 year study period.


  Materials and Methods Top


In this retrospective study, from May 2007 to May 2012, total thirteen cases of multiple malignancies diagnosed histopathologically were retrieved from the archives of department of surgical oncology. Clinical data were obtained from the medical records. We did not include leukemia as 2nd malignancy. Furthermore, autopsy data was not included. We have not included those cases where the possibility of the 2nd malignancy being a metastatic deposit was not completely excluded. We have categorized the malignancies as synchronous if the interval between development of them was less or equal to 6 months and if it was more than 6 months we have termed it as metachronous Positron Emission Tomography- Computed Tomography (PET-CT) was not done in any of these cases due to financial constraints.

In this retrospective study, the patients and their relatives have given consent to utilize the information for publication purpose as noted from the standard case sheet record obtained from the medical records department. As the study had no intervention other than standard care, we have not obtained permission from the institutional review board.


  Results Top


We retrieved a total of thirteen cases in the 5 year study period. Out of them, two were in the metachronous category owing to interval between detection of primary and 2nd malignancy being more than 6 months. The synchronous ones were detected simultaneously either at the time of clinical examination or reported in histopathological examination of the surgical specimen.

There was female predominance with age range being 43-68 years. Majority of the cases were in 7th decade. The most common organ involved was breast, followed by cervix.

In the metachronous category, there were two cases. In thefirst case, thefirst primary was (IDCC (nos)) Infiltrating duct cell carcinoma (not otherwise specified) of breast and the 2nd malignancy was endometrial adenocarcinoma. This patient was diagnosed as a case of IDCC (nos) after lumpectomy which was carried out in an outside center. After that the patient did not receive any chemo or radiotherapy. She presented to our institute after a gap of 39 months with fine needle aspiration (FNA) findings suggestive of recurrence of IDCC (nos). At that time she complained of bleeding per vaginum for which she was evaluated and ultrasonography showed thickened endometrium. The patient underwent right modified radical mastectomy (MRM) for recurrence of IDCC and was advised chemotherapy and hormonal therapy. She also underwent radical hysterectomy and the final histopathological impression was endometrial adenocarcinoma.

The 2nd metachronous case was a 37-year-old male patient in whom thefirst primary was detected as squamous cell carcinoma of penis. This patient was treated with emasculation, bilateral ilioinguinal block dissection and was referred to radiotherapy. However, the patient was lost to follow-up and presented again after a gap of 22 months. At that time, the routine chest X-ray showed a cavitary lesion in the left upper zone of lung. FNA of the lesion in the lung was proved to be adenocarcinoma of lung.

In the synchronous category, there were eleven cases. Out of them, four were bilateral carcinomas of breast. One bilateral carcinoma of breast revealed a histology of infiltrating lobular carcinoma and the rest that of IDCC (nos). These patients underwent bilateral MRM and received chemotherapy and hormonal therapy (Adriamycin + Cyclophosphamide for 6 cycles and Tamoxifen).

One case of bilateral carcinoma breast was detected simultaneously with endometrial adenocarcinoma of uterus.

In one case of IDCC breast, at the time of routine examination, cervical growth was detected. This patient underwent right MRM and radical hysterectomy. She also received chemo and hormonal therapy.

A breast lump was detected on the routine examination of a case of papillary carcinoma of thyroid, which later on proved to be IDCC (nos). She underwent total thyroidectomy and right MRM followed by chemotherapy.

In another case, the cervical biopsy distinctly showed adenocarcinoma of endocervix and cervical intraepithelial neoplasia (CIN-III) of ectocervix. This patient was advised radical hysterectomy but subsequently she was lost to follow-up.

Again in another case of squamous cell carcinoma of buccal mucosa, cervical growth (stage III B) was detected. This patient was referred for chemoradiotherapy.

Other cases, which were included in the synchronous variant from the department of surgical oncology were cervix showing changes of CIN-III and sertoli and leydig cell tumor of ovary and another case of squamous cell carcinoma of esophagus and mixed epithelial tumor of ovary, previously reported from our institute.[7],[8]

Follow-up data was available for various patients ranging from 6 to 42 months [Table 1].
Table 1: Patient characteristics

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  Discussion Top


Though, multiple primary cancers are not common, yet it is believed that the incidence is increasing. Since in patients with multiple cancers, the focus is mainly on the primary disease, there is a higher likelihood of missing incidental co-existence of another primary malignant lesion. Therefore, it is important to make an early diagnosis and administer prompt therapy in case of multiple cancers.[2]

The theory regarding the origin of majority of multiple primary cancers is that they arise as a result of random chance, but different mechanisms have been suggested to be involved in multiple primary cancers, such as the family history, immunologic and genetic defects, prolonged exposure to carcinogens, radiation and chemotherapy for the primary cancer, and field cancerization.[1],[6],[14],[15] Previously reported cases of multiple primary cancers are mainly described in the respiratory, gastrointestinal, and genitourinary systems.[16] One autopsy series has reported prostate cancer as one of the most common malignancies in patients with multiple primary cancers and also as a frequent incidental autopsy finding in elderly men.[17]

In our study, we have encountered two cases of malignancies in the metachronous category, where the primary was carcinoma breast in one case followed by endometrial carcinoma and the other one was carcinoma penis followed by adenocarcinoma of lung.

Breast cancer patients often develop a 2nd primary malignant tumor; common sites being opposite breast, endometrium and ovary with rare primary cancer of cervix.[9]

We have noted eight cases of carcinoma breast, out of them four being bilateral. According to the classification by Moertel, they fall under the Group IC category.[3] However, Tan et al. did not include bilateral carcinoma breast in their study stating that they are fairly common.[18]

In our study, there was one case of synchronous bilateral breast carcinoma and endometrial adenocarcinoma.

There were also three cases of carcinoma breast and endometrial adenocarcinoma. One of the cases was metachronous and the other two were was synchronous in nature. One of the synchronous cases had bilateral IDCC (nos) breast and endometrial adenocarcinoma. However, in one case, the patient did not give any history of treatment after excision of breast lump and subsequently had endometrial carcinoma. We could not find an association between tamoxifen use for breast carcinoma and subsequent development of endometrial adenocarcinoma, though in literature it is described that tamoxifen use of at least 60 months is associated with high risk uterine histological subtypes when compared to no tamoxifen use.[19]

We also had a synchronous case of breast carcinoma and cervical carcinoma.

Goto, et al. in their article have described a case of synchronous invasive squamous cell carcinoma and clear cell adenocarcinoma of endocervix. They also detected Human papillomavirus (HPV) 18 in the squamous cell carcinoma; but not in the clear cell adenocarcinoma.[20] In our case the cervical biopsy showed adenocarcinoma of endocervix and CIN-III of ectocervix, but the patient was lost to follow-up prior to complete evaluation.

There was also an unusual case of synchronous papillary carcinoma of thyroid and breast IDCC.

The numbers of patients with multiple cancers have recently been increasing. In the present scenario, the possibility of a 2nd or 3rd malignant lesion should be considered for patients with primary cancer. Furthermore, the importance of screening procedures should be emphasized for the early detection of malignancy before the appearance of clinical symptoms.

In our study though, we have encountered a good number of multiple cancers in a relatively short period, most of them being synchronous, still a larger multi-institutional study with longer follow-up is required to arrive at a definite conclusion regarding the true incidence of multiple primaries.


  Acknowledgment Top


We thank the Department of Medical Oncology, Radiology, Pathology, and Medical Records Department for their cooperation.

 
  References Top

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Noh SK, Yoon JY, Ryoo UN, Choi CH, Sung CO, Kim TJ, et al. A case report of quadruple cancer in a single patient including the breast, rectum, ovary, and endometrium. J Gynecol Oncol 2008;19:265-9.  Back to cited text no. 1
    
2.
Lee JS, Moon W, Park SJ, Park MI, Kim KJ, Jang LL, et al. Triple synchronous primary cancers of rectum, thyroid, and uterine cervix detected during the workup for hematochezia. Intern Med 2010;49:1745-7.  Back to cited text no. 2
    
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Moertel CG. Multiple primary malignant neoplasms: Historical perspectives. Cancer 1977;40:1786-92.  Back to cited text no. 3
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Moertel CG, Dockerty MB, Baggenstoss AH. Multiple primary malignant neoplasms. I. Introduction and presentation of data. Cancer 1961;14:221-30.  Back to cited text no. 4
    
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Iioka Y, Tsuchida A, Okubo K, Ogiso M, Ichimiya H, Saito K, et al. Metachronous triple cancers of the sigmoid colon, stomach, and esophagus: Report of a case. Surg Today 2000;30:368-71.  Back to cited text no. 5
    
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Kim SH, Kim HJ, Lee JI, Lee YS, Kang WK, Park JK, et al. Multiple primary cancers including colorectal cancer. J Korean Soc Coloproctol 2008;24:467-72.  Back to cited text no. 6
    
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Chowhan AK, Jena A, Kinnera SB, Patnayak R, Reddy OM, Reddy KM. Dual malignancy: An interesting concurrent mixed epithelial ovarian tumor with esophageal carcinoma. Indian J Cancer 2011;48:361-2.  Back to cited text no. 7
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Reddy PA, Harinarayan CV, Suresh V, Jena A, Chandrasekhar SL, Rashmi P, et al. An unusual case of virilizing ovarian tumor associated with carcinoma in situ of cervix. Int J Endocrinol Metab 2009;4:255-8.  Back to cited text no. 8
    
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Mohanti D, Pohare YH, Kumar S, Biswal BM, Kumar L. Breast cancer followed by cervix cancer: A rare form of double malignancy. Indian J Med Paediatr Oncol 1998;19:90-3.  Back to cited text no. 9
    
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Bishen KA, Singh A. A case of dual malignancy: Presenting the necessity for extensive sampling for pathologic examination. J Oral Maxillofac Pathol 2011;15:306-10.  Back to cited text no. 10
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Rajalingam R, Javed A, Gondal R, Arora A, Nag HH, Agarwal AK. Non-familial double malignancy of the colon and ampulla of Vater: A case report and review of literature. Saudi J Gastroenterol 2012;18:143-5.  Back to cited text no. 11
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Angurana SL, Kapoor R, Kumar P, Khosla D, Kumar N, Sharma SC, et al. Quadruple malignancy in a single patient: A case report and comprehensive review of literature. J Cancer Res Ther 2010;6:230-2.  Back to cited text no. 12
    
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Kumar V, Singh K, Tatke M, Rathi AK, Shekhar S, Bahadur AK. Synchronous anaplastic oligodendroglioma and carcinoma tongue: A rare association. J Cancer Res Ther 2010;6:227-9.  Back to cited text no. 13
    
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Slaughter DP, Southwick HW, Smejkal W. Field cancerization in oral stratified squamous epithelium; clinical implications of multicentric origin. Cancer 1953;6:963-8.  Back to cited text no. 14
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Li FP. Second malignant tumors after cancer in childhood. Cancer 1977;40:1899-902.  Back to cited text no. 15
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Cercato MC, Colella E, Ferraresi V, Diodoro MG, Tonachella R. Report of two cases of quintuple primary malignancies and review of the literature. Anticancer Res 2008;28:2953-8.  Back to cited text no. 16
    
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Lee TK, Myers RT, Scharyj M, Marshall RB. Multiple primary malignant tumors (MPMT): Study of 68 autopsy cases (1963-1980). J Am GeriatrSoc1982;30:744-53.  Back to cited text no. 17
    
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Tan BC. Double primary malignant neoplasms. Singapore Med J 1974;15:212-7.  Back to cited text no. 18
    
19.
Bland AE, Calingaert B, Secord AA, Lee PS, Valea FA, Berchuck A, et al. Relationship between tamoxifen use and high risk endometrial cancer histologic types. Gynecol Oncol 2009;112:150-4.  Back to cited text no. 19
    
20.
Goto K, Takeuchi Y, Yakihara A, Kotsuji F. Synchronous invasive squamous cell carcinoma and clear cell adenocarcinoma of the uterine cervix: A different human papillomavirus status. Gynecol Oncol 2005;97:976-9.  Back to cited text no. 20
    



 
 
    Tables

  [Table 1]


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