Skip to main content
Kardiochirurgia i Torakochirurgia Polska = Polish Journal of Cardio-Thoracic Surgery logoLink to Kardiochirurgia i Torakochirurgia Polska = Polish Journal of Cardio-Thoracic Surgery
. 2015 Mar 31;12(1):14–17. doi: 10.5114/kitp.2015.50562

Results of surgical treatment of primary lung cancer with synchronous brain metastases

Mariusz Jan Bella 1,2,, Janusz Kowalewski 1,2, Maciej Dancewicz 2, Przemysław Bławat 2, Tomasz Jarosław Szczęsny 2, Aleksandra Chrząstek 1,2, Paweł Wnuk 1,2
PMCID: PMC4520501  PMID: 26336472

Abstract

Introduction

The surgical treatment of non-small cell lung cancer (NSCLC) with synchronous brain matastases is more effective than other therapeutic options, but this management is still controversial.

The aim of the study

The aim of the study was to evaluate the survival of patients after pulmonary resection NSCLC preceded by resection of brain metastases.

Material and methods

From 2007 to 2012, 645 patients underwent pulmonary resection for NSCLC at our department. In 25 of them (3.87%) thoracic surgery was preceded by resection of a single brain metastasis of NSCLC and a PET CT scan. No signs of nodal involvement or distant metastases were detected.

Results

The group consisted of 18 men (72%) and 7 women (28%). Average age was 57.62 years (46-70). In all cases, whole brain radiotherapy (5 × 4 Gy) was performed. The average interval between excision of brain metastasis and lung resection was 31.4 days (27-41). Pneumonectomy was performed in 1, lobectomy/bilobectomy in 17 and wedge resection in 7 cases. Pathological stage N0 was diagnosed in 17, N1 in 5 and N2 in 3 patients. Average survival was 18.68 months (4-74). Survival at 1, 2 and 5 years was 64%, 28% and 28% respectively. Average disease-free survival was 17.52 months. Histological type (p = 0.57) and G (p = 0.82) have no influence on survival. All the patients with hilar lymph node involvement died within 26 months and with mediastinal one within 12 months.

Conclusions

Surgical treatment of patients with NSCLC with synchronous brain metastases may prove beneficial in selected patients after excluding other distant metastases and lymph node involvement.

Keywords: lung cancer, brain metastases

Introduction

Lung cancer is the leading cause of cancer death in both men and women in Poland [1]. Brain metastasis is diagnosed clinically in up to 30% of patients with non-small cell lung cancer (NSCLC) during the course of the disease [2, 3], and in autopsy series the incidence is up to approximately 60% [4]. Surgical resection of these metastatic lesions is considered in only 25% of patients [5]. Long-term survival after surgical treatment of metachronous brain metastases in patients with primary NSCLC has been reported in several studies and is promising [6, 7]. However, the results of surgical treatment of synchronous brain metastases along with the primary tumours is controversial [8, 9]. In this retrospective analysis we present our results of resection of synchronous brain metastases and of the primary NSCLC. In addition, we present prognostic factors affecting survival.

Material and methods

From January 2007 to December 2012, 645 patients underwent pulmonary resection for non-small cell lung cancer at our department. In 25 of them (3.87%) surgical treatment for single brain metastases from lung cancer was performed before thoracic surgery. Preoperative workup included positron emission tomography (PET) scan and magnetic resonance imaging or computed tomography (CT) scan of the brain. No signs of residual tumour of the brain, nodal involvement or distant metastases were detected. The medical records of these patients were reviewed. This record was examined for age, sex, histological type and grade, postoperative tumour and nodal stage, surgical procedure, adjuvant therapy and survival. Cerebral and pulmonary resection was considered radical if all macroscopic evidence of disease was removed. Postoperative staging was done according to the International Staging System for Non-Small Cell Lung Cancer (2008). Survival was estimated by the Kaplan-Meier method with the date of pulmonary resection used as the starting point and the date of death or last follow-up as the end point. The influence of variables on survival was analysed by the log-rank test for multivariate analyses.

Results

The group consisted of 18 men (72%) and 7 women (28%). Average age was 57.62 years (range 46-70). The average interval between excision of brain metastases and lung resection was 31.4 days (range from 27 to 41 days). Pneumonectomy was performed in 1 patient, lobectomy/bilobectomy in 17 and wedge resection in 7 patients (due to compromised cardio-pulmonary function). No patient had preoperative endobronchial ultrasound (EBUS) or mediastinoscopy. Adenocarcinoma was found in 13 cases, squamous-cell carcinoma in 8, large-cell carcinoma in 2 and others in 2 patients. Pathological stage N0 was diagnosed in 17 patients, N1 in 5 and N2 in 3 patients.

Whole brain radiotherapy (WBR) (5 x 4 Gy) was applied in every patient after the neurosurgical procedure, before lung resection. Postoperative adjuvant chemotherapy was given in 12 patients (48%). Patients were selected to receive adjuvant therapy at the discretion of the surgeon and consulting oncologist. Inclusion criteria for chemotherapy were mediastinal or hilar nodal involvement, grade G3 carcinoma (2 cases) and large-cell carcinoma (2 cases).

There were neither perioperative deaths nor serious perioperative complications after pulmonary resection. Follow-up was complete in all patients for a median of 19 months (range 4-74). Recurrence developed in 15 patients (60%). It was only local in 7 cases (47%) – 4 in the lung and 3 in the brain – and distant in 3 cases (12%): bone, adrenal, liver. In 5 cases (20%) both local and distant recurrence developed. No patient underwent late reoperation for recurrent brain metastases. Average survival time was 18.7 months (range from 4 to 74 months). Survival at 1, 2 and 5 years was 64%, 28% and 28% respectively. Average disease-free survival was 17.5 months. Currently, 10 patients are alive without evidence of recurrent disease (7 of them 60 months or more after pulmonary resection).

Cell type (p = 0.57) and G (p = 0.82) have no influence on survival. All the patients who had hilar metastases died within 26 months and those with mediastinal lymph node involvement within 12 months. No statistical significance was calculated because of the small number of cases. Multivariate analysis found that neither age (0.59), sex (0.61), tumour histological type (p = 0.57), grade (p = 0.82), type of pulmonary resection (p = 0.64), nor adjuvant chemotherapy (p = 0.71) affected long-term survival.

Discussion

Cisplatin-based chemotherapy is the gold standard of treatment of disseminated NSCLC [10]. However, solitary metastases to the brain, other lung and adrenal gland, especially metachronous, detected a long time after primary pulmonary resection, are believed resectable, with an acceptable cure rate [11]. The prognosis worsens when the time between treatment of primary tumour and diagnosis of metastasis is shorter, and is believed to be significantly worse for synchronous metastases [12], although some authors observed a better prognosis with synchronous metastases than metachronous brain metastases [9]. When the first symptoms of lung cancer are those caused by distant metastases, usually the only treatment is palliative chemotherapy. However, in recent years a growing role of local treatment (radiation or surgery) of solitary distant metastases has been stressed. An example is solitary metastases to the brain, which can be radically removed by the surgeon, treated with stereotactic radiosurgery (SRS) or gamma-knife radiosurgery (GKRS), often with adjuvant whole brain radiotherapy (WBRT) or systemic cytostatic chemotherapy, followed by radical resection of the primary pulmonary tumour, if no other local or distant metastases are present. This is quite a rare situation, in our series found only in 3.87% of resected patients, but, because lung cancer is the most common neoplasm, this accounts for a meaningful group of patients. Most authors agree that SRS or GKRS gives similarly good local control of brain metastases as surgical resection [1315], while WBRT is believed to provide shorter median survival [16] (15.4 months vs. 11.5 months, p = 0.002) [14]. Some data show a slightly better prognosis after surgical resection of brain metastases than after SRS [17].

It is widely accepted that after radical treatment of solitary brain metastasis, only patients without other distant metastases and without nodal metastases can be considered candidates for radical surgical treatment. Therefore in our study PET-CT screening was always performed before thoracic surgery. Positron emission tomography–computed tomography is also considered mandatory by other authors, to exclude mediastinal nodal metastases [18]. In our series preoperative staging was based on PET screening, and only patients without suspected metastases to lymph nodes were subsequently operated on. Some authors routinely performed mediastinoscopy in such patients, to exclude N2 disease [15]. However, numerous studies have proved that in patients after radical treatment of synchronous brain metastases, surgery allows better local control and longer median survival than thoracic radiation combined with chemotherapy [19, 20], although others have stressed that not the type of local thoracic treatment but response to preoperative chemotherapy was the main prognostic factor [10]. In the preoperative treatment, the MVP regimen (mitomycin, vinblastine, cisplatin) was, however, poorly tolerated in a phase II trial in NSCLC patients with solitary metastases [21], while newer chemotherapeutic agents seemed to be better tolerated [22]. However, many authors did not report any chemotherapy prior to thoracic surgery.

Similarly as in our study, many authors stress that the absence of nodal metastases is the main factor influencing long-term survival. In many series and case reports, data about cure achieved in stage I disease patients (N0) are provided [18, 23, 24], while lower T-stage was the main factor influencing survival in only one paper [25].

Conclusions

Surgical treatment of patients with NSCLC with synchronous brain metastases may prove beneficial in selected patients after excluding other distant metastases and lymph node involvement. Survival after resection of the primary tumour in patients with lymph node metastases is very poor; therefore EBUS-TBNA (transbronchial needle aspiration) or mediastinoscopy should be performed routinely in this group of patients.

Biography

graphic file with name KITP-12-24925-ig001.gif

Disclosure

Authors report no conflict of interest.

References

  • 1.Didkowska J. Epidemiologia i etiopatogeneza nowotworów płuca. In: Nowotwory płuca i opłucnej. In: Jassem J, Krzakowski M, editors. Gdańsk: Via Medica; 2009. pp. 1–14. [Google Scholar]
  • 2.Knights EM., Jr Metastatic tumors of the brain and their relation to primary and secondary pulmonary cancer. Cancer. 1954;7:259–265. doi: 10.1002/1097-0142(195403)7:2<259::aid-cncr2820070208>3.0.co;2-c. [DOI] [PubMed] [Google Scholar]
  • 3.Sørensen JB, Hansen HH, Hansen M, Dombernowsky P. Brain metastases in adenocarcinoma of the lung: frequency, risk groups, and prognosis. J Clin Oncol. 1988;6:1474–1480. doi: 10.1200/JCO.1988.6.9.1474. [DOI] [PubMed] [Google Scholar]
  • 4.Billing PS, Miller DL, Allen MS, Deschamps C, Trastek VF, Pairolero PC. Surgical treatment of primary lung cancer with synchronous brain metastases. J Thorac Cardiovasc Surg. 2001;122:548–553. doi: 10.1067/mtc.2001.116201. [DOI] [PubMed] [Google Scholar]
  • 5.Kaal EC, Niël CG, Vecht CJ. Therapeutic management of brain metastasis. Lancet Neurol. 2005;4:289–298. doi: 10.1016/S1474-4422(05)70072-7. [DOI] [PubMed] [Google Scholar]
  • 6.Macchiarini P, Buonaguidi R, Hardin M, Mussi A, Angeletti CA. Results and prognostic factors of surgery in the management of non-small cell lung cancer with solitary brain metastasis. Cancer. 1991;68:300–304. doi: 10.1002/1097-0142(19910715)68:2<300::aid-cncr2820680215>3.0.co;2-s. [DOI] [PubMed] [Google Scholar]
  • 7.Mussi A, Pistolesi M, Lucchi M, Janni A, Chella A, Parenti G, Rossi G, Angeletti CA. Resection of single brain metastasis in non-small-cell lung cancer: prognostic factors. J Thorac Cardiovasc Surg. 1996;112:146–153. doi: 10.1016/s0022-5223(96)70190-3. [DOI] [PubMed] [Google Scholar]
  • 8.Martini N. Rationale for surgical treatment of brain metastasis in non-small cell lung cancer. Ann Thorac Surg. 1986;42:357–358. doi: 10.1016/s0003-4975(10)60534-6. [DOI] [PubMed] [Google Scholar]
  • 9.Getman V, Devyatko E, Dunkler D, Eckersberger F, End A, Klepetko W, Marta G, Mueller MR. Progmosis of patients with non-small cell lung cancer with isolated brain metastases undergoing combined surgical treatment. Eur J Cardiothorac Surg. 2004;25:1107–1113. doi: 10.1016/j.ejcts.2004.02.021. [DOI] [PubMed] [Google Scholar]
  • 10.Girard N, Cottin V, Tronc F, Etienne-Mastroianni B, Thivolet-Bejui F, Honnorat J, Guyotat J, Souquet PJ, Cordier JF. Chemotherapy is the cornerstone of the combined surgical treatment of lung cancer: with synchronous brain metastases. Lung Cancer. 2006;53:51–58. doi: 10.1016/j.lungcan.2006.01.014. [DOI] [PubMed] [Google Scholar]
  • 11.Kozower BD, Lamer JM, Detterbeck FC, Jones DR. Special treatment issues in non-small cell lung cancer: Diagnosis and management of lung cancer. Chest. (3rd ed) 2013;143(5 Suppl):e369S–99S. doi: 10.1378/chest.12-2362. American College of Chest Physicians evidence-based clinical practice guidelines. [DOI] [PubMed] [Google Scholar]
  • 12.Flannery TW, Suntharalingam M, Kwok Y, Koffman BH, Amin PP, Chin LS, Nicol B, Fowler Z, Young AB, Regine WF. Gamma knife stereotactic radiosurgery for synchronous versus metachronous solitary brain metastases from non-small cell lung cancer. Lung Cancer. 2003;42:327–333. doi: 10.1016/s0169-5002(03)00357-x. [DOI] [PubMed] [Google Scholar]
  • 13.Griffioen GR, Toguri D, Dahele M, Warner A, de Haan PF, Rodrigues GB, Slotman BJ, Yaremko BP, Senan S, Palma DA. Radical treatment of synchronous oligometastatic non- small cell lung carcinoma (NSCLC): patient outcomes and prognostic factors. Lung Cancer. 2013;82:95–102. doi: 10.1016/j.lungcan.2013.07.023. [DOI] [PubMed] [Google Scholar]
  • 14.Xu Q, Wang Y, Liu H, Meng S, Zhou S, Xu J, Schmid-Bindert G, Zhou C. Treatment outcome for patients with primary NSCLC and synchronous solitary metastasis. Clin Transl Oncol. 2013;15:802–809. doi: 10.1007/s12094-013-1008-2. [DOI] [PubMed] [Google Scholar]
  • 15.Mordant P, Arame A, De Dominicis F, Pricopi C, Foucault C, Dujon A, Le Pimpec-Barthes F, Riquet M. Which metastasis management allows long-term survival of synchronous solitary M1b non-small cell lung cancer? Eur J Cardiothorac Surg. 2012;41:617–622. doi: 10.1093/ejcts/ezr042. [DOI] [PubMed] [Google Scholar]
  • 16.Kim KH, Lee J, Lee JI, Nam do H, Kong DS, Ahn YC, Park HC, Kwon OJ, Kim H, Chang MH, Yi SY, Ji SH, Park YH, Ahn IS, Park K, Ahn MI. Can up front systemic chemotherapy replace stereotactic radiosurgery or whole brain radiotherapy in the treatment of non-small cell lung cancer patients with asymptomatic brain metastases? Lung Cancer. 2010;68:258–263. doi: 10.1016/j.lungcan.2009.06.008. [DOI] [PubMed] [Google Scholar]
  • 17.Bai H, Han B. Surgical treatment for non-small cell lung cancer patients with synchronous solitary brain metastasis. Zhongguo Fei Ai Za Zhi. 2013;16:646–650. doi: 10.3779/j.issn.1009-3419.2013.12.05. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Melloni G, Bandiera A, Gregorc V, Carretta A, Ciriaco P, Vigano M, Franzin A, Bolognesi A, Picozzi P, Zannini P. Combined treatment of non-small cell lung cancer with synchronous brain metastases: a single center experience. J Cardiovasc Surg (Torino) 2011;52:613–619. [PubMed] [Google Scholar]
  • 19.Parlak C, Mertsoylu R, GUIer OC, Onal C, Topkan E. Definitive chemoradiation therapy following surgical resection or radiosurgery plus whole-brain radiation therapy in non-small cell lung cancer patients with synchronous solitary brain metastasis: a curative approach. lnt J Radiat Oneal Biol Phys. 2014;88:885–891. doi: 10.1016/j.ijrobp.2013.12.017. [DOI] [PubMed] [Google Scholar]
  • 20.Lind JS, Lagerwaard FJ, Smit EF, Postmus PE, slotman B, Senan S. Time for reappraisal of extracranial treatment options? Synchronous brain metastases from nonsmall cell lung cancer. Cancer. 2011;117:597–605. doi: 10.1002/cncr.25416. [DOI] [PubMed] [Google Scholar]
  • 21.Downey RJ, Ng KK, Kris MG, Bains MS, Miller VA, Heelan R, Bilsky M, Ginsberg R, Rusch VW. A phase II trial of chemotherapy and surgery for non-small cell lung cancer patients with a synchronous solitary metastasis. Lung Cancer. 2002;38:193–197. doi: 10.1016/s0169-5002(02)00183-6. [DOI] [PubMed] [Google Scholar]
  • 22.De Ruysscher D, Wanders R, van Baardwijk A, Dingemans AM, Reymen B, Rouben R, Bootsma G, Pitz C, van Eijsden L, Geraedts W, Baumert BG, Lambin P. Radical treatment of non-small-cell lung cancer patients with synchronous oligometastases: long-term results of a prospective phase II trial (Nct01282450) J Thorac Oncol. 2012;7:1547–1555. doi: 10.1097/JTO.0b013e318262caf6. [DOI] [PubMed] [Google Scholar]
  • 23.Funai K, Suzuki K, Sekihara K, Shimizu K, Shiiya N. Five-year tumor-free survival after aggressive trimodality therapy for T3NOMlb non-small cell lung cancer with synchronous solitary brain metastasis. Gen Thorac Cardiovasc Surg. 2012;60:370–372. doi: 10.1007/s11748-012-0007-5. [DOI] [PubMed] [Google Scholar]
  • 24.Gray PJ, Mak RH, Yeap BY, Cryer SK, Pinnell NE, Christianson LW, Sher DJ, Arvold ND, Baldini EH, Chen AB, Kozono DE, Swanson SJ, Jackman DM, Alexander BM. Aggressive therapy for patients with non-small cell lung carcinoma and synchronous brain- only oligometastatic disease is associated with long-term survival. Lung Cancer. 2014;85:239–244. doi: 10.1016/j.lungcan.2014.06.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Collaud S, Stahel R, Inci I, Hillinger S, Schneiter D, Kestenholz P, Weder W. Survival of patients treated surgically for synchronous single-organ metastatic NSCLC and advanced pathologic TN stage. Lung Cancer. 2012;78:234–238. doi: 10.1016/j.lungcan.2012.09.011. [DOI] [PubMed] [Google Scholar]

Articles from Kardiochirurgia i Torakochirurgia Polska = Polish Journal of Cardio-Thoracic Surgery are provided here courtesy of Termedia Publishing

RESOURCES