Skip to main content
Thoracic Cancer logoLink to Thoracic Cancer
. 2021 Mar 9;12(9):1445–1448. doi: 10.1111/1759-7714.13922

Stereotactic body radiation therapy for an octogenarian with pulmonary carcinosarcoma

Wei‐Lun Huang 1, Yu‐Ling Huang 2, Chieh‐Ni Kao 3, Yu‐Wei Liu 3,
PMCID: PMC8088919  PMID: 33687154

Abstract

Pulmonary carcinosarcoma is a rare lung tumor accounting for <1% of primary lung cancers, characterized by biphasic components with both carcinomatous and sarcomatous mesenchymal features. This report describes a case of pulmonary carcinosarcoma in an octogenarian who was treated with stereotactic body radiation therapy (SBRT) and whose therapeutic response was sustained for 2 years. Along with other treatment modalities, SBRT might be considered for the treatment of medically inoperable localized stage pulmonary carcinosarcoma.

Keywords: Octogenarian, pulmonary carcinosarcoma, SBRT, stereotactic body radiation therapy


Isodose distribution of the patient receiving total dose of 60 Gy of SBRT in three dimensions of computed tomography.

graphic file with name TCA-12-1445-g001.jpg

INTRODUCTION

Pulmonary carcinosarcoma (PC) is a rare lung tumor making up <1% of primary lung cancer cases and characterized by biphasic components of both carcinomatous and sarcomatous mesenchymal features. 1 , 2 Few cases have been reported in the literature, and even fewer large cohort studies have been published, most focusing on pathology. 3 , 4 , 5 Because of its rarity, the clinicopathological features and factors affecting survival of PC are not thoroughly understood. Although surgery remains the mainstay treatment for potentially operable disease and physically fit lung cancer patients, we demonstrate how we used stereotactic body radiation therapy (SBRT) to successfully treat a male octogenarian patient with advanced chronic obstructive pulmonary disease (COPD) diagnosed as having localized PC.

CASE REPORT

An 85‐year‐old male heavy‐smoker presented with chronic cough and shortness of breath that had lasted over 2 months. Chest radiography revealed suspicious right lung mass and chest computed tomography (CT) showed a 5.5 cm mass over right lower lobe (Figure 1(a)). CT‐guided tumor biopsy was performed in December 2018. Pathology report and immunohistochemistry suggested high probability of carcinosarcoma with squamous and osteogenic differentiations (Figure 2). After a complete staging investigation of positron emission tomography scan (Figure 3) and brain magnetic resonance imaging, we finally diagnosed the patient as having clinical T3N0M0 stage IIB pulmonary carcinosarcoma. Because the patient had poor lung function (FEV1 = 0.4 L; FEV1/FVC = 55%) resulting from advanced COPD and medically inoperable condition, we treated him using SBRT. Standard four‐dimensional CT simulation was performed. The maximum intensity projection of gross lesion was defined as internal target volume (ITV). The planning target volume (PTV) was determined based on the ITV with a margin of 5 mm. Treatment was delivered using volumetric modulated arc therapy (VMAT). Prescribed SBRT dose was 60 Gy in eight fractions (7.5 Gy per fraction) (Figure 4). SBRT plan was optimized to achieve D95 PTV (dose received by 95% volume) of 100%. Mean bilateral lung dose was 6.129 Gy. The volume of lung receiving a dose of 5 Gy (V5) was 24.2%, 10 Gy (V10) was 19.2%, and 20 Gy (V20) was 10%. Maximum dose to spinal cord was 18.319 Gy. The patient tolerated the therapy well without grade 2–5 toxicities throughout the treatment period. Thereafter, he received regular outpatient clinical follow‐ups and chest CT scan every 6 months for 2 years, demonstrating sustained good local control of the tumor (Figure 1(b)–(e)). At present, the patient has been physically well and free from any clinical suspicion of recurrence for 24 months since SBRT.

FIGURE 1.

FIGURE 1

Chest computed tomography (CT) of the pulmonary carcinosarcoma. (a) Chest CT showed a 5.5 cm right lower lung mass. (b) Follow‐up CT 6 months after SBRT revealed a notable shrinkage in the lung tumor. (c) Follow‐up CT 12 months after SBRT revealed sustained therapeutic response. (d) Follow‐up CT 18 months after SBRT still showed sustained therapeutic response. (e) Follow‐up CT 24 months after SBRT revealed sustained therapeutic response of the lung tumor without evidence of recurrence

FIGURE 2.

FIGURE 2

Microscopic features of the tumor. (a) Squamous cell carcinoma component of the tumor positive for the p40 (×100). (b) Epithelial component of the tumor positive for cytokeratin AE1/AE3 (×100). (c) Sarcoma component showing spindle tumor cells positive for vimentin (×200). (d) Focally positive for SATB2 (×100)

FIGURE 3.

FIGURE 3

Positron emission tomography scan of the patient. (a) and (b) The scan revealed an increased F‐18 fluorodeoxyglucose (FDG) uptake mass lesion (SUVmax = 31.8) over right lower lung without evidence of hilar/mediastinal lymph node metastasis

FIGURE 4.

FIGURE 4

The prescription isodose level in SBRT plan. Isodose distribution of the patient receiving total dose of 60 Gy of radiation in eight fractions in the axial plane (a), coronal plane (b), and sagittal plane (c)

DISCUSSION

The results of our staging work‐ups showed localized disease that is usually treated surgically. However, after weighing the risks and benefits of surgery on an elderly person with extremely poor lung function, we believed that nonsurgical therapy would be safer and opted to use SBRT. To the best of our knowledge, this is the first report of the successful use of SBRT to treat localized PC.

Recently, Ersek et al. 6 reporting an analysis of the surveillance, epidemiology, and end results (SEER) for PC, found that surgical resection alone had better survival than other treatment modalities or combination therapies for this disease. Furthermore, another study, also using SEER database, sought to identify the prognostic factors and determine optimal treatment for PC. 7 That study found the factors male gender, age, T4 stage, M1 stage, surgery, and chemotherapy to be independently associated with PC survival. If we considered the two SEER analyses together without more investigation, the standard treatment for managing pulmonary carcinosarcoma with localized disease would undoubtedly be surgical resection. However, chemotherapy or radiotherapy is preferred over surgical resection for the treatment of advanced stage PC, making survival outcome inherently poor and possibly explaining their reported differences in survival outcome in those studies. In addition, the authors of the former SEER analysis 6 suggested that because radiotherapy may be performed less in the localized stage PC patients who potentially prefer operative therapy. It is not known what the precise dosage of delivered radiotherapy was to the patients across the long timespan of the survey (1973–2012).

SBRT has become an effective treatment modality for medically or surgically inoperable lung cancer, and in one study, it has proven to provide superior survival benefit to the conventional fractionated radiotherapy. 8 Over the past decade, more clinicians have become aware of SBRT and have begun using it more often to treat early‐stage lung cancer in both medically inoperable and operable patients. 9 , 10 It has also been used to treat much older patients (>80 years old) with high efficacy and tolerable toxicities. 11 , 12 Therefore, the potential benefit of SBRT in medically inoperable patients with PC should not be underestimated.

According to the literature to date, for medically inoperable or advanced PC patients, in addition to radiotherapy, chemotherapy has demonstrated some therapeutic efficacy. 13 , 14 Targeted therapy with pazopanib has also been found to have a favorable treatment response in metastatic PC. 15 Therefore, our report of this case may bring welcome news to those seeking more therapeutic options for inoperable or advanced PC.

In conclusion, we reported the first use of SBRT to treat pulmonary carcinosarcoma to have an evident beneficial therapeutic response. SBRT might be considered an additional therapeutic option along with other treatment modalities when determining optimal care for pulmonary carcinosarcoma in some patients.

DISCLOSURE

The authors have nothing to disclose.

ACKNOWLEDGMENT

The authors thank James Steed for his help with language revision.

Huang W‐L, Huang Y‐L, Kao C‐N, Liu Y‐W. Stereotactic body radiation therapy for an octogenarian with pulmonary carcinosarcoma. Thorac Cancer. 2021;12:1445–1448. 10.1111/1759-7714.13922

REFERENCES

  • 1. Yang H, Lin Y, Liang Y. Treatment of lung carcinosarcoma and other rare histologic subtypes of none‐small cell lung cancer. Curr Treat Options Oncol. 2017;18:54. [DOI] [PubMed] [Google Scholar]
  • 2. Travis WD, Brambilla E, Nicholson AG, Yatabe Y, Austin JHM, Beasley MB, et al. The 2015 World Health Organization classification of lung tumors: impact of genetic, clinical and radiologic advances since the 2004 classification. J Thorac Oncol. 2015;10:1243–60. [DOI] [PubMed] [Google Scholar]
  • 3. Braham E, Ben Rejeb H, Aouadi S, et al. Pulmonary carcinosarcoma with heterologous component: report of two cases with literature review. Ann Transl Med. 2014;2:41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Olobatoke AO, David D, Hafeez W, van T, Saleh HA. Pulmonary carcinosarcoma initially presenting as invasive aspergillosis: a case report of previously unreported combination. Diagn Pathol. 2010;5:11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Kim KI, Flint JD, Muller NL. Pulmonary carcinosarcoma: radiologic and pathologic findings in three patients. AJR Am J Roentgenol. 1997;169:691–4. [DOI] [PubMed] [Google Scholar]
  • 6. Ersek JL, Symanowski JT, Han Y, Howard A, Dumas K, Ahrens W, et al. Pulmonary Carcinosarcoma: a surveillance, epidemiology, and end results (SEER) analysis. Clin Lung Cancer. 2020;21(2):160–70. [DOI] [PubMed] [Google Scholar]
  • 7. Sun L, Dai J, Wang X, Jiang G, Gonzalez‐Rivas D, Song J, et al. Pulmonary carcinosarcoma: analysis from the surveillance, epidemiology and end results database. Interact Cardiovasc Thorac Surg. 2020;30(1):4–10. [DOI] [PubMed] [Google Scholar]
  • 8. Newman NB, Sherry AD, Byrne DW, Osmundson EC. Stereotactic body radiotherapy versus conventional radiotherapy for early‐stage small cell lung cancer. J Radiat Oncol. 2019;8(2):239–48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Khorfan R, Kruser TJ, Coughlin JM, Bharat A, Bilimoria KY, Odell DD. Survival of primary stereotactic body radiation therapy compared with surgery for operable stage I/II non‐small cell lung cancer. Ann Thorac Surg. 2020;110(1):228–34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Ostheimer C, Evers C, Palm F, Mikolajczyk R, Vordermark D, Medenwald D. Mortality after radiotherapy or surgery in the treatment of early stage non‐small‐cell lung cancer: a population‐based study on recent developments. J Cancer Res Clin Oncol. 2019;145:2813–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Bei Y, Murakami N, Nakayama Y, Okuma K, Kashihara T, Raturi VP, et al. Stereotactic body radiation therapy for early‐stage non‐small‐cell lung cancer in octogenarian and older: an alternative treatment. J Radiat Res. 2020;61(4):586–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Kreinbrink P, Blumenfeld P, Tolekidis G, Sen N, Sher D, Marwaha G. Lung stereotactic body radiation therapy (SBRT) for early‐stage non‐small cell lung cancer in the very elderly (≥80years old): extremely safe and effective. J Geriatr Oncol. 2017;8(5):351–5. [DOI] [PubMed] [Google Scholar]
  • 13. Saint‐Georges F, Terrier P, Sabourin JC, Bonvalot S, De Montpreville V, Ruffie P. Pulmonary carcinosarcoma with jejunal metastasis: complete response to chemotherapy. Rev Pneumol Clin. 2002;58(4 Pt 1):249–52. [PubMed] [Google Scholar]
  • 14. Langer F, Wintzer HO, Werner M, Weber C, Brümmendorf TH, Bokemeyer C. A case of pulmonary carcinosarcoma (squamous cell carcinoma and osteosarcoma) treated with cisplatin and doxorubicin. Anticancer Res. 2006;26:3893–7. [PubMed] [Google Scholar]
  • 15. Tanimoto A, Takeuchi S, Kotani H, Yamashita K, Yamada T, Ohtsubo K, et al. Pulmonary carcinosarcoma showing an obvious response to pazopanib: a case report. BMC Pulm Med. 2018;18(1):193. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Thoracic Cancer are provided here courtesy of Wiley

RESOURCES