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Clinicopathological characteristics of resected adenosquamous cell carcinoma of the lung: Risk of coexistent double cancer
Journal of Cardiothoracic Surgery volume 5, Article number: 92 (2010)
adenosquamous carcinoma (ADSQ) of non-small cell lung cancer (NSCLC) is a rare disease and the biological behavior and clinicopathological characteristics have not yet been thoroughly described.
This study reviewed the patient charts of 11 (1.6%) ADSQ cases among 779 patients with primary lung cancer who underwent a lung resection. The characteristics and clinicopathological factors were evaluated retrospectively.
Six of the 11 patients with ADSQ were male and five were female. The mean age was 67.3 years' olds. Three patients had pathological stage IA, one patient each had stage IB and IIA, five patients had stage IIIA, and one patient stage IIIB. Five patients had coexistent double cancer including 2 gastric, 1 rectal, 1 prostate and 1 bladder cancer. ADSQ was found less frequently in males than squamous cell carcinoma (SQ). ADSQ was found more frequently in older patients, with advanced stage, advanced T status, and lymph node metastases than adenocarcinoma (AD). The proportion with coexistent double cancer of AD, SQ, and ADSQ were 21.1, 17.6, and 45.5%, respectively. ADSQ had a significantly correlation with double cancer (ADSQ vs. non- ADSQ p = 0.03). A multivariate analysis showed no significant prognostic difference between the patients with ADSQ and non- ADSQ.
In this study, cases with ADSQ showed no significantly prognostic difference in comparison to AD and SQ. However, surgeons must be cautious of any coexistent double cancer because approximately half of all patients with ADSQ of the lung have double cancer.
Lung cancer remains the most common cause of cancer death worldwide . Despite recent improvements in diagnostic technologies, more than 50% of patients present locally advanced or distant metastatic disease, and the prognosis still remains unsatisfactory [2, 3]. One reason for this is that the specific characterization of phenotype according to the pathological diagnosis has not been clarified, especially with regard to minor phenotypes, such as ADSQ  and large cell neuroendocrine carcinoma . There are few reports of the clinical significance of ADSQ [6–9]. The effectiveness of surgical resection of ADSQ of the lung remains poorly defined because of the relatively low frequency of this type of tumor [6, 7]. Shimizu. et al. reported that the survival rates for patients with ADSQ were statistically worse than for patients with SQ and AD, due to the highly aggressive pathological stage of ADSQ . On the other hand, Hsia et al. reported that the prognostic behavior of ADSQ had no influence on survival in comparison to the survival curves with those for SQ and AD  consistent with previous reports [8, 9]. Therefore, the prognostic impact of ADSQ in lung cancer still remains controversial. Furthermore, no series has addressed the correlation between the ADSQ and coexistent double cancer. This study retrospectively reviewed cases a 13-year period to clarify the correlation between the ADSQ and clinicopathological factors including coexistent double cancer and to elucidate the prognostic significance of ADSQ of the lung in comparison to the AD and SQ.
Materials and methods
Patients and methods
The characteristics and clinicopathological factors were evaluated retrospectively. Seven hundred and seventy-nine patients with primary lung cancer underwent a surgical resection between April 1994 to March 2006 at the Second Department of Surgery at University of Occupational and Environmental Health, Kitakyushu, Japan. Of these, 403, 187, 39, 24, 11, 125, and 10 patients were diagnosed as AD, SQ, large cell carcinoma, small cell carcinoma, ADSQ, multiple primary lung cancer (MPLC), and others, respectively. According to the established criteria, on routine microscopic examination using hematoxylin and eosin staining, a sample from a tumor containing at least 20% each of AD and SQ is classified as ADSQ . Specimens from each of these patients were reviewed critically by one (S.Y.) pathologist. This study evaluated 11 cases (1.6%) with ADSQ among 779 resected primary lung cancers. The characteristics of the patients with ADSQ are shown in Table 1. They included 6 males and 5 females with a mean age of 67.3 years, ranging in age from 48 to 79 years. Of these eleven patients, all had undergone complete resections, and six were N0 cases. The pathological stages of the cancer were stage IA in 3 patients, IB in 1, IIA in 1, IIIA in 5, IIIB in 1, according to the TNM classification revised by the International union Against Cancer . Patients were followed up with clinical assessments, chest X-rays, and tumor marker every month during the first year and every 3 months thereafter after operation. Computed tomography, bone scintigram and brain magnetic resonance imaging were all performed every 6 months. The mean observation period was 46.1 months.
Statistical analyses were performed using the Stat view 5.0 software program for Windows (Abacus Concepts, Inc., California). The chi-square test was used to assess the relationship between ADSQ and each of the clinicopathological features. In the prognostic analysis, the Kaplan-Meier method was used to estimate the probability of survival, and survival differences were analyzed by the log-rank test. A multivariate analysis was performed according to Cox's proportional hazards model. A p-value less than 0.05 was considered to be significant.
The clinical features of ADSQ patients
The clinical features of the patients with ADSQ are summarized in Table 1. The most frequent symptoms were cough. They included 8 smokers and 3 never smokers. Bronchoscopic examination indicated that the tumor was centrally located in two cases and was peripherally located in nine cases. All patients underwent bronchoscopy, and the results of biopsy or cytology revealed a malignancy in 7 (63.6%). The preoperative pathological diagnosis was SQ in three patients, non-small cell lung carcinoma in two patients and AD in one patient. The preoperative cytological diagnosis without definite pathological diagnosis was AD in one patient. All patients underwent a lobectomy except for one pneumonectomy. Five of 11 patients received postoperative adjuvant therapy including chemotherapy in 4 patients and radiation in one patient. Six patients had recurrent disease after surgery and the mean disease free interval was 56.5 months. Three of the 6 patients received chemotherapy treatment. Five of 11 (45.5%) patients had coexistent double cancer. Two patients had gastric cancer, and one patient each had prostate, bladder, and rectal cancer, respectively. Five patients died due to a recurrence of lung cancer. Complete follow-up data were available on all patients.
Histological type between the primary lesion and lymph node metastasis
The prevalent histological differentiation of AD was moderately differentiated (45%, 5/11), while the prevalent SQ was moderately differentiated in 82% (9/11; Table 2). The two elements identified were either in contiguous fields or intermingling, and the ratios between the two yielded three groups. In 3 tumors, the AD component exceeded the SQ component. In 7 tumors, the reverse was true. Only one case showed both components present in roughly equal quantities. Lymph node metastases were found in 6 cases (55%) and were more frequent in cases with a larger SQ component in the primary lesion (Table 3).
Relationship between ADSQ and clinicopathological factors
When the clinicopathological factors were compared by AD, the status of ADSQ did not significantly affect the sex and coexistent double cancer. However, an ADSQ was found more frequently in old age, advanced stage, advanced T status, and N status. When the clinicopathological factors were compared by SQ, the status of ADSQ did not significantly affect the age, pathological stage, T status or N status. However, an ADSQ was found more frequently in females and coexistent double cancers (Table 4). ADSQ also showed a significant correlation with coexistent double cancers (ADSQ vs. non- ADSQ p = 0.03).
Influence of ADSQ on overall survival
A univariate analysis showed no significant prognostic difference between the patients with old age, histological type divided into ADSQ, coexistent double cancer, and MPLC. Meanwhile males, advanced T, and N status were associated with an unfavorable prognosis (Table 5). The five-year survival of AD, SQ, and ADSQ was 71.4, 55.8, and 50.6%, respectively. A multivariate analysis included such factors as sex, age, T status, N status, histological type, coexistent double cancer, and MPLC. Though, no significant prognostic difference was identified between the patients with regard to histological type, coexistent double cancer, and MPLC, the prognosis for patients with male sex, old age, advanced T, and N status was significantly worse, compared with the patients for counter features (Table 6).
The classification of lung carcinoma into a small cell lung carcinoma (SCLC) and NSCLC is highly reproducible. However, there are few studies about ADSQ with anecdotal reports on the subtype of ADSQ. ADSQ of the lung is a subset of pulmonary carcinomas, and comprises less than 4% of lung carcinomas [4, 6–8]. It is quite difficult to diagnose ADSQ preoperatively . In fact, only seven of 11 patients were diagnosed NSCLC as either AD and SQ. Interestingly, the preoperative pathological diagnosis was judged to the AD in case 1, nevertheless the preoperative cytological diagnosis was SQ by washing and brushing cytology under bronchoscopy. Physicians should therefore suspect ADSQ in cases where there is this type of preoperative mixed diagnosis.
This study identified no significant prognostic difference was identified between the patients with ADSQ and non-ADSQ. These findings are consistent with Hsia's data . However, other researchers report the highly aggressive behavior of ADSQ [6, 7, 12–14]. This discrepancy might be attributed to three main factors. The first is that the current study observed very few patients with ADSQ. Due to the infrequent occurrence of this disease, no series reported to date has been of adequate size for a definitive statistical analysis. The second possibility is a previous international discrepancy in the pathological recording. At the present, Japanese lung cancer society defines ADSQ as tumor composed of SQ and AD components of at least 20% each . However, previous World Health Organization histological classifications did not refer to the ratio of these two components and recent classification has required a minimum of 10% of each component. The third possibility may be the discrepancy among the pathological diagnosis .
This is the first report to address the problem of coexistent double cancer with ADSQ. In general, the prevalence of coexistent double cancer for the patients with lung cancer is about 10% of lung carcinomas . Surprisingly, almost half of all patients with ADSQ of the lung were observed to have coexistent double cancer. Some clinical experiences have been reported  based on the concept of filed carcinogenesis in specific organ system such as respiratory or gastrointestinal tract, which are consistent with the current. Thus, behavior of tumor with ADSQ might be amore aggressive than the tumor with AD or SQ. It is necessary to suspect the presence of double cancer not only in the medical examination for the patients before treatment of ADSQ, but also during the follow-up after a complete resection.
Carcinogenesis is a multi-step gene abnormality and requires a certain amount of time to progress. ADSQ was found more frequently in old age than AD in this study suggesting that age is the one of the main risk factors for this type of cancer. Heterogeneity is frequent in cancer and ADSQ is an atypical heterogeneous tumor containing two distinct components of AD and SQ. Therefore, the current findings, which show a high prevalence of coexistent double cancer, suggest the cancer cells not only consist of mixture of AD and SQ, but also show progression of carcinogenesis with specific mechanisms in separate organs. The original histogenesis remains unclear. However, the biological impact is very interesting because the squamous cell component does not exist in the peripheral lung. Lymph node metastases were more frequent in cases with a larger SQ component in the primary lesion in this study. Therefore characterization of ADSQ may be a first step based on carcinogenesis to resolve the mystery of the heterogeneity. The histogenesis of ADSQ includes some possibilities including AD with squamous metaplasia, collision tumor, high-grade mucoepidermoid carcinoma, and bi-potential undifferentiated cell origin . Niho et al. showed that SQ and AD components showed identical monoclonal patterns, suggesting that the SQ and AD components originate from the same cell . Kanazawa et al. also reported the clonal expansion in the carcinogenic process by the monoclonal transition from SQ to AD in ADSQ . Therefore, the histogenesis of ADSQ might represent a phase in ongoing differentiation from a common cancer stem cell.
In conclusion, this current study demonstrated that ADSQ is an unusual histological subtype of NSCLC and approximately half of the patients with ADSQ had coexistent double cancer, thus suggesting that cancer cells in ADSQ demonstrate progressive carcinogenesis with specific mechanisms.
squamous cell carcinoma
non small cell lung cancer
small cell lung carcinoma
multiple primary lung cancer
- 95% CI:
95% confidence interval.
Pirozynski M: 100 yars of lung cancer. Respir Med. 2006, 100: 2073-84. 10.1016/j.rmed.2006.09.002.
Mountain CF: Revisions in the International System for Staging Lung Cancer. Chest. 1997, 111: 1710-7. 10.1378/chest.111.6.1710.
van Rens MT, de la Rivière AB, Elbers HR, van Den Bosch JM: Prognostic assessment of 2,361 patients who underwent pulmonary resection for non-small cell lung cancer, stage I, II, and IIIA. Chest. 2000, 117: 374-9. 10.1378/chest.117.2.374.
Hsia JY, Chen CY, Hsu CP, Shai SE, Wang PY: Adenosquamous carcinoma of the lung. Surgical results compared with squamous cell and adenocarcinoma. Scand Cardiovasc J. 1999, 33: 29-32. 10.1080/14017439950142000.
Iyoda A, Hiroshima K, Nakatani Y, Fujisawa T: Pulmonary large cell neuroendocrine carcinoma: its place in the spectrum of pulmonary carcinoma. Ann Thorac Surg. 2007, 84: 702-7. 10.1016/j.athoracsur.2007.03.093.
Nakagawa K, Yasumitu T, Fukuhara K, Shiono H, Kikui M: Poor prognosis after lung resection for patients with adenosquamous carcinoma of the lung. Ann Thorac Surg. 2003, 75: 1740-4. 10.1016/S0003-4975(03)00022-5.
Shimizu J, Oda M, Hayashi Y, Nonomura A, Watanabe Y: A clinicopathologic study of resected cases of adenosquamous carcinoma of the lung. Chest. 1996, 109: 989-94. 10.1378/chest.109.4.989.
Sridhar KS, Bounassi MJ, Raub W, Richman SP: Clinical features of adenosquamous lung carcinoma in 127 patients. Am Rev Respir Dis. 1990, 142: 19-23.
Ishida T, Kaneko S, Yokoyama H, Inoue T, Sugio K, Sugimachi K: Adenosquamous carcinoma of the lung. Clinicopathologic and immunohistochemical features. Am J Clin Pathol. 1992, 97: 678-85.
Japan Lung Cancer Society: general a rule for clinical and pathological record dog lung cancer. 2003, Tokyo: Kanehara publishing, 6th edition.
Sobin LH, Wittekind C: TNM classification of malignant tumors. 2002, New York: Wiley, 6
Naunheim KS, Taylor JR, Skosey C, Hoffman PC, Ferguson MK, Golomb HM, Little AG: Adenosquamous lung carcinoma: clinical characteristics, treatment, and prognosis. Ann Thorac Surg. 1987, 44: 462-6. 10.1016/S0003-4975(10)62102-9.
Kamiyoshihara M, Hirai T, Kawashima O, Ishikawa S, Morishita Y, Maeshima A: A clinicopathologic study of the resected cases of adenosquamous carcinoma of the lung. Oncol Rep. 1998, 5: 861-5.
Takamori S, Noguchi M, Morinaga S, Goya T, Tsugane S, Kakegawa T, Shimosato Y: Clinicopathologic characteristics of adenosquamous carcinoma of the lung. Cancer. 1991, 67: 649-54. 10.1002/1097-0142(19910201)67:3<649::AID-CNCR2820670321>3.0.CO;2-B.
Ghandur-Mnaymneh L, Raub WA, Sridhar KS, Albores-Saavedra J, Gould E, Duncan RC: The accuracy of the histological classification of lung carcinoma and its reproducibility: a study of 75 archival cases of adenosquamous carcinoma. Cancer Invest. 1993, 11: 641-51. 10.3109/07357909309046936.
Luciani A, Ascione G, Marussi D, Oldani S, Caldiera S, Bozzoni S, Codecà C, Zonato S, Ferrari D, Foa P: Clinical analysis of multiple primary malignancies in the elderly. Med Oncol. 2009, 26: 27-31. 10.1007/s12032-008-9075-x.
Curtis RE, Boice JD, Kleinerman RA, Flannery JT, Fraumeni JF: Summary: multiple primary cancers in Connecticut, 1935-82. Natl Cancer Inst Monogr. 1985, 68: 219-42.
Ichinose Y, Hara N, Takamori S, Maeda K, Yano T, Ohta M: DNA ploidy pattern of each carcinomatous component in adenosquamous lung carcinoma. Ann Thorac Surg. 1993, 55: 593-6. 10.1016/0003-4975(93)90257-I.
Niho S, Yokose T, Kodama T, Nishiwaki Y, Mukai K: Clonal analysis of adenosquamous carcinoma of the lung. Jpn J Cancer Res. 1999, 90: 1244-7.
Kanazawa H, Ebina M, Ino-Oka N, Shimizukawa M, Takahashi T, Fujimura S, Imai T, Nukiwa T: Transition from squamous cell carcinoma to adenocarcinoma in adenosquamous carcinoma of the lung. Am J Pathol. 2000, 156: 1289-98.
This work was supported by a Grand-in Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
The authors declare that they have no competing interests.
This report reflects the opinion of the authors and does not represent the official position of any institution or sponsor. The contributions of each of the authors were as follows:
HU were responsible for reviewing previous research, journal handsearching, drafting report. SY was responsible for pathological data. TH was responsible for quality checking and data processing. HU was responsible for project coordination. All authors have read and approved the final manuscript.
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Uramoto, H., Yamada, S. & Hanagiri, T. Clinicopathological characteristics of resected adenosquamous cell carcinoma of the lung: Risk of coexistent double cancer. J Cardiothorac Surg 5, 92 (2010). https://doi.org/10.1186/1749-8090-5-92
- Clinicopathological Factor
- Small Cell Carcinoma
- Neuroendocrine Carcinoma
- Primary Lung Cancer
- Large Cell Carcinoma