Research Article | Vol. 5, Issue 3 | Journal of Neuro and Oncology Research | Open Access

Clinical and Demographic Outcomes of Brain Metastases Receiving Whole Brain Radiation: A Retrospective Study from a Tertiary Care Institute in Eastern India

 

Bijayalaxmi Sahoo1, Sandip Kumar Barik2*, Pragateshnu Das3, Deepak Das2, Anupam Muraleedharan2, Soel Ahmed2, Priyanka Mukherjee2, Saroj Kumar Das Majumdar2, Dillip Kumar Parida2

1Department of Radiation Oncology, Kalinga Institute of Medical Science, Bhubaneswar, India
2Department of Radiation Oncology, All India Institute of Medical Sciences, Bhubaneswar, India
3Department of Neurology, Kalinga Institute of Medical Sciences, Bhubaneswar, India

*Correspondence author: Sandip Kumar Barik, MD, Associate Professor, Department of Radiation Oncology, All India Institute of Medical Sciences, Sijua PO Patrapada, Bhubaneswar, Odisha, India; Email: [email protected]

Citation: Sahoo B, et al. Clinical and Demographic Outcomes of Brain Metastases Receiving Whole Brain Radiation: A Retrospective Study from a Tertiary Care Institute in Eastern India. J Neuro Onco Res. 2025;5(3):1-10.

Copyright© 2025 by Sahoo B, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Received
01 September, 2025
Accepted
29 September, 2025
Published
06 October, 2025

Abstract

Background: Brain Metastasis (BM) is associated with poor prognosis. It affects the Quality of Life (QOL) and causes significant morbidity. BMs are the most common intracranial neoplasm, with a total number that outnumber primary neoplasms by a ratio of 10:1. In the present study, we aim to analyze the clinicodemographic profile and treatment outcomes of brain metastasis. Also, try to identify factors associated with survival in patients with brain metastasis.

Methods: A retrospective, single-institutional study of 151 patients with brain metastases was conducted from January 2018 to May 2019. Medical records were reviewed to collect demographic and clinical information. The aim was to analyze the demographic and clinical profiles of patients with brain metastasis. Additionally, it analyzes patient factors, tumor characteristics and treatment plans that may impact overall survival in patients with brain metastases.

Results: The median age for diagnosis of brain metastasis was 50 years. 82 patients were male. The common primary metastasizing to the brain was lung carcinoma (61%), followed by breast carcinoma (16%). 58% had adenocarcinoma histology and 14% of patients had infiltrating ductal carcinoma. (54%) showed multiple metastases, which is more common than a single metastasis (39%). 7% of patients showed two sites of metastases. 60% of patients have Supratentorial lesions. 29% of patients showed both supra and infratentorial lesions. Among them, the frontal lobe was the most commonly involved site. Out of 151 patients, 90 patients showed frontal lobe metastasis. Parietal and cerebellar metastasis is the next common site for metastasis 60% of patients are diagnosed upfront for brain metastasis. 3% of patients developed brain metastasis after five years of primary diagnosis. The most commonly used dose prescription for Whole Brain Radiation (WBRT) is 30Gy/10 fractions or 20Gy/5 fractions. 54% patients treated with 30Gy/10fx dose prescription. Median survival for patients with brain metastasis was eight months (ranging from 1 month to 32 months). Younger age (40-50 years), breast primary with a single metastasis and developed brain metastasis after 1-2 years of primary diagnosis were associated with better survival.

Conclusion: The study highlights that in patients with brain metastasis, the overall prognosis remains poor; however, younger patients (40-50 years) and those with a single brain lesion demonstrate relatively better survival outcomes. Other factors, such as gender, WBRT dose and site of lesion, did not significantly affect survival.

Keywords: Brain Metastasis; Carcinoma Lung; Clinicodemographic Profile; Median Survival; Multiple Lesions

Abbreviations

BM: Brain Metastasis; WBRT: Whole Brain Radiotherapy; CE-MRI: Contrast Enhanced Magnetic Resonance Imaging

Introduction

Brain Metastasis (BM) is the most common intracranial neoplasm in adults and occurs in 10-30% of adults with disseminated tumors [1,2]. Brain metastasis is usually diagnosed between the 5th and 7th decades of life [3]. An estimated 20% of all cancer patients develop brain metastasis. Most brain metastases originate from the Lungs, Breast, Colorectal carcinoma and Melanoma [4]. Hematological neoplasm constitutes only 10% of all brain metastases and primarily affects the leptomeninges [5,6]. Adenocarcinoma and small cell carcinoma of the lungs are the most common histologies associated with brain metastasis. 80% of cases of BMs are located in the cerebral hemisphere, followed by 15% in the cerebellum and 5% in the brainstem [7]. The frontal lobe has been reported to be the most frequent site of metastasis within the brain [8]. However, primary cancer type and specific biological features strongly influence the site preferences of central nervous system spread.

In recent years, brain metastasis has increased due to improved diagnosis by advanced imaging techniques, prolonged survival due to advanced anti-cancer treatment and the brain being a pharmacological sanctuary site due to the blood-brain barrier [9-11].

The clinical presentation of brain metastasis is similar to other intracranial neoplasms, like headache (30-60%), cognitive impairment (30%), seizure, focal neurological deficit, ataxia, nausea and vomiting [12,13]. At diagnosis, 60-70% of patients can be asymptomatic [14]. Contrast-Enhanced Magnetic Resonance Imaging (CE-MRI) is the cornerstone for diagnosing brain metastasis. The radiological features of cerebral metastasis are multiple and typically present at the grey-white matter junction or in arterial watershed areas.

Brain metastasis itself added an adverse factor in the primary disease due to its impact on Survival and Quality of Life. The prognosis of the patients with BMs has been inferior, with a median overall Survival of 1-2 months if any treatment for brain metastasis [15].  Considering the above, this study was designed to retrospectively analyze the demographic and clinical profiles of patients with brain metastasis and evaluate their survival. This study also analyzed the correlation between various clinicodemographic factors and survival.

Methods

A total of 151 patients were retrospectively analyzed who were treated with radiation therapy for brain metastasis between January 2018 and May 2019. Patients with a histologically proven primary site with brain metastasis were included and all data about these patients were entered in a standardized case record form.

Study Variables: The parameters documented included age, gender, primary site, stage, histology of the primary tumor, site of metastasis, number of brain metastases, any other site of metastasis (excluding the brain) and survival in months.

Statistics

Data were entered into a Microsoft Excel spreadsheet for statistical analysis and then analyzed by SPSS 29.0. Data were summarized as means, medians and standard deviations for numerical variables and counts and percentages for categorical variables. Kaplan-Meier curves were plotted to evaluate survival and the log-rank test was used for univariate analysis. P-value ≤ 0.05 was considered for statistical significance.

Results

In the study, out of 151 patients, 47 patients (31%) were between 40 and 50 years of age and 45 patients (29%) were between 50 and 60 years of age. So, the maximum number of patients (60%) are between the 40-60 age group. The age range was from 20 to 75 years. There were no significant differences in the distribution of brain metastases by gender. Male patients (n=82) are slightly more 54% than female patients (n=69). Lung cancer was the most common primary (61%) for metastasis to the brain, followed by Ca Breast (16%) (Fig. 1).

Figure 1: Bar diagram depicting the primary site giving rise to brain metastasis.

When analyzing different histologies of the primary site, 58% of the patients have adenocarcinoma histology, followed by 14% of patients with infiltrating duct carcinoma. Few cases have squamous and Adenocarcinoma (Fig 2).

Figure 2: Bar diagram showing histology of primary.

Of 151 patients, 54% (n = 82) showed multiple metastases and 39% (n = 58) had a single metastasis. 7% of patients (n = 11) have only two metastases (Fig. 3).

Figure 3: Pie diagram showing the distribution of patients according to the number of brain metastases.

Most metastases (60%) were located in the supratentorial region, while 11% were located in the infratentorial region. 29% of patients showed lesions in both supra-tentorial and infratentorial locations (Fig. 4).

Figure 4: Pie diagram showing different locations of brain metastasis (supratentorial, infratentorial or both).

Among them, the frontal lobe is the most common site of brain metastasis. Of 151 patients, 90 (59%) had frontal lobe metastasis. 58 patients (38%) had parietal and cerebellar metastasis. Two patients also showed meningeal metastasis and both had primary hematological malignancy. 82 Patients (54%) showed bilateral involvement. Of the remaining patients, 27% had left-sided brain involvement and 19% had right-sided involvement, with no statistically significant result (Fig. 5).

Figure 5: Bar diagram depicting distributions of patients according to different lobes of brain involvement.

In this study, out of 151 patients, 105 patients (70%) had uncontrolled primary tumors and 46 patients (30%) had controlled primary tumors during the diagnosis of brain metastasis.

Headache is the most common presenting symptom, followed by vomiting and Focal Neurological Disease (FND). 78 patients presented with headaches and 44 patients with vomiting. 35 patients don’t have any symptoms. They were all diagnosed through an evaluation, which included a CE-MRI scan of the brain. 26 patients presented with other symptoms like head reeling, dizziness, vision problems and scalp pain.

In this study, 35% of patients exhibited only brain metastasis, while 65% had metastasis at another site in addition to the brain. Out of these, 65% of patients have bone metastasis as the most common site (28%), followed by lung and liver metastasis. 16% of patients showed another site of metastasis, like the adrenal gland, kidney, skin nodules or retroperitoneal lymph node.

Most patients with brain metastasis (60%) are diagnosed upfront during primary evaluation. Only five patients (3%) developed brain metastasis five years after diagnosis of the primary. 20 patients (13%) developed brain metastasis within 1-2 years of diagnosing the primary disease. The most common dose prescriptions for Whole Brain Radiation Therapy (WBRT) are 30Gy/10 fractions and 20Gy/5 fractions. In our study, 54% of patients received 30Gy in 10 fractions and 43% received 20Gy in 5 fractions. Only 3% of patients were treated with other dose prescriptions, such as 25Gy/10 fractions, 30Gy/15 fractions and 25Gy/5 fractions, depending on the patient’s performance status. All the clinicodemographic parameters are summarized in Table 1.

SL No

Variables

Group

No of Patients (Percentage)

1

Age Group in Years

<20

20-30

30-40

40-50

50-60

60-70

>70

0 (0%)

4 (2.64%)

18 (11.9%)

47 (31.12%)

45 (29.8%)

29 (19.2%)

8 (5.29%)

2

Gender

Male

Female

82 (54.3%)

69 (45.69%)

3

Primary

Lung

Breast

Esophagus

Gastrointestinal

Genito-Urinary

Gynaecological

Head And Neck

Lymphoma

Melanoma

Pancreato-Biliary

Other

93 (61.5%)

25 (16.5%)

1 (0.66%)

8 (5.29%)

4 (2.64%)

3 (1.98%)

7 (4.63%)

2 (1.32%)

1 (0.66%)

5 (3.31%)

2 (1.32%)

4

Histology

Adenocarcinoma

Idc

Small Cell Carcinoma

Squamous Cell Carcinoma

Other

89 (58.9%)

22 (14.5%)

6 (3.97%)

14 (9.27%)

20 (13.2%)

5

No. of Mets

Single

Two

Multiple

58 (38.4%)

11 (7.28%)

82 (54.3%)

6

Tentorial Site

Supratentorial

Infratentorial

Both

89 (58.9%)

17 (11.2%)

44 (29.1%)

7

Lobe of Brain

Frontal

Parietal

Temporal

Occipital

Cerebellar

Deep Gray Matter

Brainstem

Meningeal

90 (59.6%)

58 (38.4%)

28 (18.5%)

25 (16.5%)

58 (38.4%)

24 (15.8%)

5 (3.31)

2 (1.32%)

8

Site of Involvement

Right

Left

Bilateral

28 (18.5%)

41 (27.1%)

82 (54.3%)

9

Primary Disease Status

Controlled

Uncontrolled

46 (30.4%)

105 (69.5%)

10

Symptoms

Headache

Vomiting

Seizure

Fnd

Ataxia

Other

No Symptoms

78 (51.6%)

44 (29.1%)

8 (5.29%)

33 (21.8%)

10 (6.62%)

26 (17.2%)

35 (23.1%)

11

Other Sites of Metastasis

No

Lung

Liver

Bone

Other

67 (44.3%)

22 (14.5%)

19 (12.5%)

55 (36.4%)

30 (19.8%)

12

Duration for Bm Diagnosis

Upfronts

0-1

1-2

2-3

3-4

4-5

>5

91 (60.2%)

18 (11.9%)

20 (13.2%)

10 (6.62%)

3 (1.98%)

4 (2.64%)

5 (3.31%)

13

Dose Prescription

20gy

30gy

Other

65 (43.0%)

81 (53.6%)

5 (3.31%)

Table 1: Clinicodemographic parameters.

Table 1: Clinicodemographic parameters.

SL No

Parameter

Value

1.

Mean (In Months)

9.07

2.

Standard Error of Mean

0.446

3.

Median (In Months)

8

4.

Mode (In Months)

7

5.

Standard Deviation

5.487

6.

Variance

30.102

7.

Minimum

1 Month

8.

Maximum

32 Months

Table 2: Survival factors.

Univariate Analysis (Table 3).

SL No

Parameter

Group

Survival In Months

Chi-Square

P Value

1.

Age

20-30

30-40

40-50

50-60

60-70

>70

8

8

9

8

7

7

142

0.041

2.

Gender

Male

Female

8

8

22.23

0.506

3.

Primary

Breast

Lung

Other

9

8

8

242.479

0.273

4.

Histology

Adenocarcinoma

Idc

Other

8

8.5

8

100.41

0.832

5.

Number of Mets

Single

Two

Multiple

8.5

8

8

122.61

0.001

6.

Tentorial

Supratentorial

Infratentorial

Both

8

8

8.5

83.89

0.715

7.

Primary Disease Status

Controlled

Uncontrolled

8

8

50.238

0.309

8.

Duration Of Brain Mets Diagnosis (In Years)

Upfront

0-2

2-5

>5

8

9

8

8

114.37

0.93

9.

Dose In Gray

20

30

OTHER

8

8

9

25.95

0.303

Table 3: Survival according to analyzed parameters.

Survival With Age

The median survival for a patient with brain metastasis is nine months for the age group of 40-50 years and for the age group of > 60 years, it is only seven months. This result is statistically significant (p < 0.041) (Fig. 6).

Figure 6: Showing the Kaplan Meier Survival Curve.

Survival With Gender

The median survival was eight months for both male and female genders without a statistically significant result (p=0.506).

Survival With Primary Cancer Site

Median survival after diagnosis of brain metastasis is nine months in patients with breast cancer (n=25) and eight months for lung cancer primary (n=93) and other malignancies (n=33). However, this result was not statistically significant (p = 0.273).

Survival With Histology of Primary

The median survival for patients with infiltrating ductal carcinoma was 8.5 months and for all other histologies, eight months, without any statistically significant result (p=0.832).

Survival With the Number of Brain Metastasis

The median survival times were eight months for patients with multiple lesions and 8.5 months for those with a single lesion. This difference is the statistical significance (p=0.001).

Survival With Lesion Site

The median survival was eight months for both supratentorial and infratentorial lesions, with a survival rate of 8.5 months for both groups. However, this result was not statistically significant (p = 0.715).

Survival With Primary Tumour Status

The median survival was eight months for both patients with controlled and uncontrolled primary disease (p = 0.309).

Survival With Duration of Metastasis

The survival was only eight months for patients with an upfront diagnosis of brain metastasis. The patients were diagnosed within 0-2 years; the survival rate was nine months. Again, the survival was only eight months for patients diagnosed with brain metastasis after two years (p=0.93).

Survival With Treatment

The survival rate was eight months for patients treated with either dose prescriptions of 30Gy/10 fractions or 20Gy/5 fractions (p = 0.303).

Discussion

Brain metastasis is the most common intracranial neoplasm in adults. It occurs in 10-30% of adults with disseminated tumors (1). 1,00,000-1,70,000 new brain metastasis cases are diagnosed annually in the United States [12]. A study by Victor showed that about 60% of patients with brain metastasis are aged between 50 and 70 years [16]. Similarly, in our study, the median age was 50 years (ranging from 20 to 75 years), with 60% of patients falling within the 40- to 60-year age range. In this study, the age of diagnosis significantly affects survival, with better outcomes in the 40-50 years age group (p < 0.041). 

Brain metastasis is most commonly associated with lung primary (40-50%), followed by Breast and melanoma [4]. In our study, lung carcinoma constituted 61%, followed by breast cancer at 16%. Out of all lung primaries, 58% were adenocarcinoma histology, followed by 3% small cell carcinoma. 14% of patients showed infiltrating duct carcinoma histology. Brain metastasis is primarily diagnosed synchronously in 60% of cases and less commonly metachronous in 40%. The study by Nussbausm and Delattre, et al., showed that approximately 80% of Brain metastatic lesions are in the cerebrum, 15% in the cerebellum and 5% in the brainstem [17]. In our study, 60% of the cases showed a supratentorial location. According to the location in different lobes, the frontal lobe is the most common site of BMs (n = 90), followed by the parietal lobe (n = 58). Only 0.5% of patients showed meningeal metastasis, which is more common in hematological malignancies.

The most common symptoms of BMs included headache, vomiting, seizure, focal neurological deficit and ataxia. Victor, et al., study showed headache (42%) and seizure (21%) are the two most common presenting symptoms [16]. In the present study, 78 patients presented with headaches, followed by 44 patients with vomiting and 35 patients were asymptomatic. A study by Victor opined that brain secondaries are most common in patients with uncontrolled primary tumors [16]. 70% of our patients had an uncontrolled primary, which indicates that brain metastasis mainly develops in patients with an uncontrolled primary.

The decision regarding treatment for brain metastasis depends on the patient’s performance status, the number of brain metastases, the status of the primary disease and the presence of metastases in other organs. Management strategies for brain metastasis include surgery, Whole-Brain Radiotherapy (WBRT), Stereotactic Radiosurgery (SRS) and Stereotactic Radiotherapy (SRT) [18]. Doses for WBRT are typically 30Gy in 10 fractions or 20Gy in 5 fractions. This two-fractionation schedule does not differ in terms of symptom control or overall survival.[19] In this study, 54% of patients were treated with WBRT at 30Gy/10 fractions and 43% with 20Gy/5 fractions. Only 3% of patients received prescriptions for any other dose. Similar to the Borgelt, et al., study, our study showed a comparable overall survival of 8 months for patients treated with either dose prescription. Popper, et al., showed that lung cancer has a greater propensity to spread to the bone, adrenal glands and brain [20]. 65% of patients exhibited metastasis to sites other than the brain. Out of this, the bone is the most common site of metastasis (28%). Other common sites of metastasis are the liver and adrenal glands.

Out of 151 patients, 43 patients survived up to 6 months. In our study, the Median Survival was eight months (range, 1 to 32 months). Our analysis yielded similar survival rates to those reported by Ekici, et al., with a median survival of 6.7 months [21]. They also identified a patient with a single brain metastasis from a controlled primary tumor who had better survival. The younger age group (40-50 years old) with single brain lesions had better survival, with a statistically significant result (p < 0.05) in our study. Rostagi, et al., identified that female gender, performance status, breast primary, metachronous brain metastasis, solitary outcome and controlled primary were associated with better survival in brain metastasis [22].

Limitations

It employs a retrospective and non-randomized design. So, a larger sample size and disease-specific graded factors for each disease site could reveal more factors affecting survival. SRS or SBRT treatment may improve survival in patients with limited lesions and a controlled primary tumor.

Conclusion

This study highlights that brain metastasis is most common in elderly males with lung adenocarcinoma, with the frontal lobe being the predominant site. Most lesions were multiple and the most common WBRT prescription was 30Gy in 10 fractions. While the overall prognosis remains poor, younger patients (40-50 years) and those with a single brain lesion demonstrated relatively better survival outcomes. Other factors, such as gender, WBRT dose and site of lesion, did not significantly affect survival. These findings should be consolidated with a larger prospective study.

Conflict of Interests

The authors have no conflict of interest to declare related to this article.

Funding

No source of funding for this study.

References

  1. Muacevic A, Wowra B, Siefert A, Tonn JC, Steiger HJ, Kreth FW. Microsurgery plus whole brain irradiation versus Gamma Knife surgery alone for treatment of single metastases to the brain: A randomized controlled multicentre phase III trial. J Neurooncol. 2008;87(3):299-307.
  2. Arita H, Narita Y, Miyakita Y, Ohno M, Sumi M, Shibui S. Risk factors for early death after surgery in patients with brain metastases: Reevaluation of the indications for and role of surgery. J Neurooncol. 2014;116(1):145-52.
  3. Johnson JD, Young B. Demographics of brain metastasis. Neurosurg Clin N Am. 1996;7(2):337-44.
  4. Achrol AS, Rennert RC, Anders C. Brain metastases. Nat Rev Dis Primers. 2019;5:5.
  5. Barnholtz-Sloan JS, Sloan AE, Davis FG, Vigneau FD, Lai P, Sawaya RE. Incidence proportions of brain metastases in patients diagnosed (1973 to 2001) in the Metropolitan Detroit Cancer Surveillance System. J Clin Oncol. 2004;22(14):2865-72.
  6. Schouten LJ, Rutten J, Huveneers HAM, Twijnstra A. Incidence of brain metastases in a cohort of patients with carcinoma of the breast, colon, kidney and lung and melanoma. Cancer. 2002;94(10):2698-705.
  7. Patchell RA. Metastatic brain tumors. Neurol Clin. 1995;13(4):915-25.
  8. Cacho-Díaz B, Lorenzana-Mendoza NA, Chávez-Hernandez JD, González-Aguilar A, Reyes-Soto G, Herrera-Gómez Á. Clinical manifestations and location of brain metastases as prognostic markers. Curr Probl Cancer. 2019;43(4):312-23.
  9. Cherryman G, Golfieri R. Comparison of spin echo T1-weighted and FLASH 90° gadolinium-enhanced magnetic resonance imaging in the detection of cerebral metastases. Br J Radiol. 1990;63(752):712-5.
  10. Mintz AH, Kestle J, Rathbone MP, Gaspar L, Hugenholtz H, Fisher B, et al. A randomized trial to assess the efficacy of surgery in addition to radiotherapy in patients with a single cerebral metastasis. Cancer. 1996;78(7):1470-6.
  11. Nolan C, Deangelis LM. Overview of metastatic disease of the central nervous system. Handb Clin Neurol. 2018;149:3-23.
  12. Sawaya R, Wildrick DM. Metastatic brain tumors: Surgery perspective. In: Chin LS, Regine WF, editors. Principles and practice of stereotactic radiosurgery. New York: Springer. 2008;193-9.
  13. Posner JB. Brain metastases: 1995. A brief review. J Neurooncol. 1996;27(3):287-93.
  14. Soffietti R, Cornu P, Delattre JY. EFNS Guidelines on diagnosis and treatment of brain metastases: Report of an EFNS Task Force. Eur J Neurol. 2006;13(7):674-81.
  15. Zimm S, Wampler GL, Stablein D, Hazra T, Young HF. Intracerebral metastases in solid-tumor patients: Natural history and results of treatment. Cancer. 1981;48(2):384-94.
  16. Saha A, Ghosh SK, Roy C, Choudhury KB, Chakrabarty B, Sarkar R. Demographic and clinical profile of patients with brain metastases: A retrospective study. Asian J Neurosurg. 2013;8(3):157-61.
  17. Nussbaum ES, Djalilian HR, Cho KH, Hall WA. Brain metastases. Histology, multiplicity, surgery and survival. Cancer. 1996;78(8):1781-8.
  18. Tsao MN, Rades D, Wirth A. Radiotherapeutic and surgical management for newly diagnosed brain metastasis(es): An American Society for Radiation Oncology evidence-based guideline. Pract Radiat Oncol. 2012;2(3):210-25.
  19. Borgelt B, Gelber R, Kramer S, Brady LW, Chang CH, Davis LW, et al. The palliation of brain metastases: Final results of the first two studies by the radiation therapy oncology group. Int J Radiat Oncol Biol Phys. 1980;6(1):1-9.
  20. Popper HH. Progression and metastasis of lung cancer. Cancer Metastasis Rev. 2016;35(1):75-91.
  21. Ekici K, Temelli O, Dikilitas M, Dursun IH, Bozdag Kaplan N, Kekilli E. Survival and prognostic factors in patients with brain metastasis: Single center experience. J BUON. 2016;21(4):958-63.
  22. Rastogi K, Bhaskar S, Gupta S, Jain S, Singh D, Kumar P. Palliation of brain metastases: analysis of prognostic factors affecting overall survival. Indian J Palliat Care. 2018;24(3):308-12.

Bijayalaxmi Sahoo1, Sandip Kumar Barik2*, Pragateshnu Das3, Deepak Das2, Anupam Muraleedharan2, Soel Ahmed2, Priyanka Mukherjee2, Saroj Kumar Das Majumdar2, Dillip Kumar Parida2

1Department of Radiation Oncology, Kalinga Institute of Medical Science, Bhubaneswar, India
2Department of Radiation Oncology, All India Institute of Medical Sciences, Bhubaneswar, India
3Department of Neurology, Kalinga Institute of Medical Sciences, Bhubaneswar, India

*Correspondence author: Sandip Kumar Barik, MD, Associate Professor, Department of Radiation Oncology, All India Institute of Medical Sciences, Sijua PO Patrapada, Bhubaneswar, Odisha, India; Email: [email protected]

Bijayalaxmi Sahoo1, Sandip Kumar Barik2*, Pragateshnu Das3, Deepak Das2, Anupam Muraleedharan2, Soel Ahmed2, Priyanka Mukherjee2, Saroj Kumar Das Majumdar2, Dillip Kumar Parida2

1Department of Radiation Oncology, Kalinga Institute of Medical Science, Bhubaneswar, India
2Department of Radiation Oncology, All India Institute of Medical Sciences, Bhubaneswar, India
3Department of Neurology, Kalinga Institute of Medical Sciences, Bhubaneswar, India

*Correspondence author: Sandip Kumar Barik, MD, Associate Professor, Department of Radiation Oncology, All India Institute of Medical Sciences, Sijua PO Patrapada, Bhubaneswar, Odisha, India; Email: [email protected]

Copyright© 2025 by Sahoo B, et al. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation: Sahoo B, et al. Clinical and Demographic Outcomes of Brain Metastases Receiving Whole Brain Radiation: A Retrospective Study from a Tertiary Care Institute in Eastern India. J Neuro Onco Res. 2025;5(3):1-10.