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MP 8.01.45 Intracavitary Balloon Catheter Brain Brachytherapy for Malignant Gliomas or Metastasis to the Brain

 

Medical Policy    
Section
Therapy
Original Policy Date
02/2007
Last Review Status/Date
Reviewed with literature search/4:2013
Issue
4:2013
  Return to Medical Policy Index

Disclaimer

Our medical policies are designed for informational purposes only and are not an authorization, or an explanation of benefits, or a contract.  Receipt of benefits is subject to satisfaction of all terms and conditions of the coverage.  Medical technology is constantly changing, and we reserve the right to review and update our policies periodically.

 


 

Description

Intracavitary balloon catheter brain brachytherapy is an approach to localized radiation therapy delivered with an inflatable balloon catheter in the treatment of malignant brain lesions.

Background

Intracavitary Balloon Catheter Brain Brachytherapy

Intracavitary balloon catheter brain brachytherapy is localized radiation therapy in the brain that requires placement of an inflatable balloon catheter in the surgical cavity, before closing the craniotomy of a resection, to remove or debulk a malignant brain mass. A radiation source is then placed in the balloon to expose surrounding brain tissue to radiation, either continuously or in a series of brief treatments. After the patient completes therapy, the radiation source is permanently removed and the balloon catheter is surgically explanted.

At present, the GliaSite® Radiation Therapy System (GliaSite® RTS; IsoRay Medical, Inc,) is the only device marketed in the U.S. for intracavitary balloon catheter brachytherapy in the brain. It includes a catheter tray with a double balloon catheter and accessories used for implantation of an aqueous saline solution of molecularly bound radioactive iodine (sodium 3 [I-125] iodo-4-hydroxybenzenesulfonate; Iotrex™) as the radiation source; and an access tray with items used for afterloading and retrieving the radioactive material. One to 3 weeks after resection and balloon implantation, the Iotrex™ solution is loaded through a subcutaneous port and left in for 3 to 6 days. Prescribed radiation doses are usually 40–60 Gy measured at 0.5–1.0 cm from the balloon surface. This procedure has been performed on an inpatient basis; however, feasibility of outpatient GliaSite® RTS implantation has been explored. (1) The GliaSite® RTS received 510(k) marketing clearance from the U.S. Food and Drug Administration (FDA) in 2001, as substantially equivalent to separately marketed ventricular reservoirs and catheters, manual radionuclide applicator systems, and radionuclide sources. In 2011, the modified GliaSite® RTS received 510(k) marketing clearance.

Malignant Gliomas

Diffuse fibrillary astrocytoma is the most common glial brain tumor in adults. It is classified histologically into 3 grades: grade II astrocytoma, grade III anaplastic astrocytoma, and grade IV glioblastoma multiforme (GBM). Oligodendrogliomas (ODGs) are diffuse neoplasms closely related to diffuse fibrillary astrocytomas clinically and biologically. However, these tumors generally have better prognoses than diffuse astrocytomas, with mean survival times of 10 years versus 2 to 3 years. Also, ODGs apparently are more chemosensitive than astrocytomas. GBM, the most aggressive and chemoresistant astrocytoma, has survival times of less than 2 years for most patients.

Treatment of primary brain tumors begins with surgery with curative intent or optimal tumor debulking, usually followed by radiation therapy and/or chemotherapy. Survival after chemoradiotherapy largely depends on the extent of residual tumor after surgery. Therefore, tumors arising in the midline, basal ganglia, or corpus callosum or those arising in the eloquent speech or motor areas of the cortex have a particularly poor outcome, since they typically cannot be extensively resected. Recurrence is common after surgery for malignant gliomas, even if followed by chemoradiotherapy, because the tumors are usually diffusely infiltrating and develop resistance to chemotherapy; also, neurotoxicity limits cumulative doses of whole-brain radiation. Chemotherapy regimens for gliomas usually rely on nitrosourea alkylating agents (carmustine or lomustine), temozolomide, procarbazine, vincristine, and platinum-based agents. The most common regimen combines procarbazine, lomustine (also known as CCNU), vincristine (PCV) and single or multi-agent therapy with temozolomide. A biodegradable polymer wafer impregnated with carmustine (Gliadel®; Guilford Pharmaceuticals, Inc.) also can be implanted into the surgical cavity as an adjunct to surgery and radiation. It is indicated for newly diagnosed high-grade malignant glioma and for recurrent GBM.

Brain Metastasis from Other Primary Malignancies

Intracranial metastases are a frequent occurrence seen at autopsy in 10–30% of deaths from cancer. Lung cancer is the most common source of brain metastasis (relative prevalence, 48%), followed by breast cancer (15%), unknown primary (12%), melanoma (9%), and colon cancer (5%).

Treatment goals in these patients include local control of existing metastases, regional control to prevent growth of undetected metastases, extending the duration of overall survival (OS), and maintaining quality of life. Surgical resection followed by whole-brain radiation therapy (WBRT) is the mainstay of treatment for patients with 1 to 3 operable brain metastases and with adequate performance status and control of extracranial disease. Resection plus WBRT extends the duration of survival, when compared with biopsy plus WBRT. Although adding WBRT to resection does not increase OS duration, it reduces local and distant recurrence of brain metastases. Thus, WBRT decreases the incidence of death from neurological causes and may help maintain adequate quality of life, if the cumulative dose does not cause unacceptable neurotoxicity.


Policy

Intracavitary balloon catheter brain brachytherapy is considered investigational, alone or as part of a multimodality treatment regimen, for primary or recurrent malignant brain tumors.

Intracavitary balloon catheter brain brachytherapy also is considered investigational, alone or as part of a multimodality treatment regimen, for metastasis to the brain from primary solid tumors outside the brain.


Policy Guidelines

There are no CPT codes specific to implantation of this type of balloon catheter. It is possible that the provider may use CPT code 64999 (unlisted procedure, nervous system).

The administration of the radiation source would likely be coded using one of the CPT codes for radiation source application (77761–77763) or remote afterloading of high dose brachytherapy (77785–77787).

There is a HCPCS code specific to the radiation solution used in this procedure:

A9527: Iodine I-125 sodium iodide solution, therapeutic, per mci.


 Benefit Application

BlueCard/National Account Issues

State or federal mandates (e.g., FEP) may dictate that all FDA-approved devices may not be considered investigational, and thus these devices may be assessed only on the basis of their medical necessity.

 


 

Rationale

This policy was originally created in 2007 and was updated regularly with searches of the MEDLINE database. The most recent literature search was performed for the period of February 2012 through February 2013. For newly diagnosed glioblastoma multiforme (GBM) patients treated after surgery, one prospective (2) and one retrospective (3) study were identified. Several studies have focused on patients treated after surgery for recurrent glioma. (4-8) Additionally, there has been one study published on patients treated for newly diagnosed and resected single brain metastasis. (9) An additional study on 8 patients with glioma or brain metastasis focused on computed tomography (CT) scan and magnetic resonance imaging (MRI) after balloon placement but did not report patient outcomes. (10)

Malignant gliomas and astrocytoma

In 2003, Tatter et al. reported on a multicenter safety and feasibility trial of the GliaSite® Radiation Therapy System (RTS) device for recurrent high-grade gliomas (n=21; 15 with GBM; 5 with anaplastic astrocytoma, and one with anaplastic oligodendrogliomas [ODG]). (4) All patients (n=11) received first-line therapy with resection and radiation, with or without systemic chemotherapy. Time from end of first-line therapy to repeated resection for recurrent disease was not reported. Although not a primary endpoint, median overall survival (OS) was 12.7 months (95% confidence interval [CI]: 6.9–15.3), and a Kaplan-Meier curve showed estimated OS at 1 year as just over 50%. Investigators reported no serious device-related adverse events during brachytherapy and no symptomatic radiation necrosis during follow-up.

Gabayan and colleagues reported on a retrospective multi-institutional analysis of the GliaSite® RTS device for recurrent high-grade gliomas in 2006 (n=95; 80 with GBM, 9 with anaplastic astrocytoma, 4 with anaplastic ODG, and one each with a mixed anaplastic tumor or gliosarcoma). (7) All patients received external-beam radiation after initial resection, and 55 (58%) also received systemic chemotherapy. Time from end of front-line therapy to repeated resection for recurrent disease was not reported. Fifteen patients (16%) who had previously been treated with external-beam radiation following maximal debulking surgery were treated with GliaSite® (average dose of 60 Gy) upon tumor recurrence. Median OS from the time of GliaSite® placement was 9.1 months (95% CI: 7.8–10.4), and OS at 1 year was 31.1% (95% CI: 21.2–41.0%). Only 2 patients experienced Radiation Therapy Oncology Group (RTOG) grade-3 toxicity attributable to radiation, and none experienced grades 4 or 5. However, 10 adverse events were attributed to surgery. The authors concluded that survival benefit was modest and that these data were similarly inconclusive to previous feasibility studies.

The retrospective analysis on GliaSite® (7) did not report important prognostic factors available from the Gliadel® randomized trial (e.g., median interval from first operation; cumulative radiation dose and proportion given whole-brain radiation therapy [WBRT] vs. local radiation vs. both in first-line therapy and completeness of the second resections). The authors concluded that it is a challenge to assess survival value from these studies without better comparative evidence on demonstrably similar patient groups, preferably from a randomized comparative trial.

Wernicke and colleagues conducted a single institution, dose escalation study to investigate the safety and feasibility of GliaSite® following surgical resection of localized newly diagnosed and recurrent brain tumors. (11, 12) The balloon was implanted during surgery in 10 consecutive patients; then 2 to 3 weeks later, aqueous solution of 125-I was introduced for times ranging from 68 to 120 hours. Median total dose was 52 Gy. Median survival for this cohort was 14 months. There were no reports of RTOG grade-3 or -4 toxicities. Similarly to the other studies cited, results from this trial suggest that the GliaSite® radiation therapy system is relatively safe and well-tolerated in patients with localized brain tumors. However, further studies would be required to assess efficacy.

In 2011, Gobitti and colleagues reported on 15 patients treated with GliaSite® brachytherapy after surgical resection of recurrent grade 3 or 4 gliomas (10 with GBM, 4 anaplastic astrocytoma, and 1 anaplastic xanthoastrocytoma). (8) Patients were followed from 1-30 months. Only 2 patients survived to 30 months follow-up. Eleven patients experienced local tumor recurrence. After GliaSite® brachytherapy, median overall survival was 13 months and median disease-free survival was 7 months. Late radiation necrosis was experienced by 3 patients; 2 subsequently died of further complications. One patient had hemiparesis and dysphagia, which resolved over 6 months. The authors concluded that re-intervention followed by GliaSite brachytherapy should not be offered as a standard treatment for recurrent high-grade glioma, because of the high rate of late complications, treatment-related deaths, and high treatment costs.

Glioblastoma multiforme

Johannesen et al. reported a Phase I/II study on 44 newly diagnosed glioblastoma multiforme (GBM) patients implanted with intracavitary balloon catheters at resection. (2) Two to 3 days after surgery, high dose-rate 192-Ir sources were inserted twice daily for 15 minutes over 5 to 6 days, using remote after-loading devices designed and fabricated by the investigators. Cumulative radiation doses were 60 (n=33) or 72 Gy (n=11). Median survival was 11.7 months (range: 2.7 to 50.9 months) for all patients, 12.8 months for those treated with 60 Gy, and 9.9 months for those treated with 72 Gy. Overall survival at 1 year was 46%. Relapses occurred in 89% of patients at a median follow-up time of 8.3 months after treatment (range: 1.2 to 34.7 months). These outcomes are similar to those of conventional WBRT after resection, although investigators emphasized the shorter treatment time (1 vs. 5 to 6 weeks) with balloon catheter brachytherapy. While the authors asserted that hospital stays were shorter (median, 21 days) and quality of life over the first 6 months was better than after conventional WBRT, they did not report data to support these claims.

In the multicenter, retrospective study performed by Welsh et al., (3) data were compiled from 8 centers on 20 patients with GBM patients with median age and Karnofsky performance status of 59 and 89, respectively. Following maximal tumor debulking, patients were treated with GliaSite® (median dose 60 Gy) prior to external-beam radiation (median dose 110 Gy). In this cohort, average survival was 11.4 months (range 4-29), 4 months longer than historical controls (95% CI: 0.23–4.9). RTOG grade-3 central nervous system toxicity was observed in 3 patients (14%). It is noteworthy that 50% of treatment failures had the balloons placed 2 cm or more from the margin of the tumor. While this study may suggest that administration of increased doses (up to 100 Gy) using GliaSite® is feasible and relatively well-tolerated, the authors acknowledge that putative survival advantage must be interpreted with caution. Additional studies using GliaSite® in conjunction with external-beam radiation following surgery for newly diagnosed GBM would be required to adequately assess safety and efficacy.

In an additional clinical trial (n=24) on recurrent GBM performed at Johns Hopkins Medical Center, (5) investigators reported results to be inconclusive. Front-line therapy included surgery followed by external-beam radiation. Time from primary resection (or from end of primary treatment) to recurrence was not reported. Median OS was 23.3 months (range, 9.3–64.1 months) from diagnosis of the primary tumor, and 9.1 months (range: 1.3–23.6 months) from GliaSite® RTS treatment. Kaplan-Meier analyses showed OS at 1 year to be approximately 33%. GliaSite® was relatively well-tolerated in this cohort with few serious adverse events. Acute adverse effects were reportedly mild; 1 patient experienced mild nausea and vomiting, and 10 experienced mild to moderate headaches. Late complications included 1 case of global aphasia and 2 incidents of symptomatic necrosis.

Finally, Payne et al. published a case report of one patient with GBM undergoing implantation with 2 brachytherapy balloons; however, there are no additional studies assessing the 2-balloon approach. (6)

Brain metastasis from other primary solid malignancies

A prospective, multicenter, Phase II trial (9) enrolled 71 patients with 1 to 3 brain metastases from a solid tumor of distant origin. Patients enrolled received either GliaSite® (n=62) or standard brachytherapy with Iotrex solution (n=54). Outcomes were analyzed without an intention-to-treat model. Primary malignancies included non-small-cell lung (54%) and gastrointestinal tract (13%) cancers, melanoma (13%), renal carcinoma (6%), and others (15%). While most patients (57%) had only brain metastases, many (43%) also had extracranial metastases. Prior therapies varied widely and included no treatment (22%), surgery (31%), surgery and radiation (33%), or surgery in addition to chemotherapy followed by radiation (24%). The investigators estimated local control at 1 year was 79%, and the median duration of local control was greater than 16.5 months. Median OS was 10 months (95% CI: 7.8–15), OS at 1 year was 40%, and median duration of functional independence was 10 months (95% CI: 7.3–20.8). Symptomatic imaging changes led to repeated operation in 13 patients, 9 of whom had radiation necrosis, 2 had mixed tumor and necrosis, and 2 had tumor recurrence only. A total of 9 grade-3 and 1 grade-4 toxicities were reported in the treated population.

Investigators indirectly compared the rate of local control in the GliaSite®-treated population: 79% with historical data showing 80–90% local control after resection plus WBRT and only 40% after resection only. However, an accompanying editorial cautions that the rate of new metastases elsewhere in the brain was 50% by 1 year after treatment and attributes this to omission of WBRT. (13) The editorial also stresses the need for direct comparative evidence to determine whether neurocognitive function and quality of life are adequately maintained for longer durations with initially focal treatment and WBRT at recurrence or with focal treatment immediately combined with WBRT.

Safety considerations

Overall, adverse events with GliaSite® are not greatly varied from those observed with other brain brachytherapy techniques; however, in 2008, Adkison and colleagues reported a case in which linens of a patient with the GliaSite® implant were contaminated with radiation. (14) Recovery studies confirmed that systemic absorption is greater than anticipated. Adkison et al. concluded that precaution with a Foley catheter should be taken in patients with urinary incontinence. Some cases of brain hemorrhage have been reported, so careful coagulation control is critical. (15)

Chino and colleagues examined feasibility of outpatient GliaSite® brachytherapy in 37 patients. (1) Rather than overnight hospitalization, patients were released after the treatment sessions. Although the study was small and ultimately inconclusive, the outpatient approach did not appear to increase adverse events and seemed to be generally well-tolerated.

Ongoing Clinical Trials

A search of online site ClinicalTrials.gov did not identify any active trials on intracavitary balloon catheter brain brachytherapy.

Summary

Intracavitary balloon catheter brain brachytherapy is an approach to localized radiation therapy delivered with an inflatable balloon catheter in the treatment of malignant brain lesions. To date, no standard medical care is established for primary brain malignancies or brain metastases of solid tumors, and there are no clinical data available to provide convincing evidence that intracavitary balloon brachytherapy extends the duration of survival, time-to-relapse, quality of life, or time-to-progression. Therefore, the use of intracavitary balloon brachytherapy for brain cancer and brain metastases of solid tumors remains investigational.

Practice Guidelines and Position Statements

The National Comprehensive Cancer Network (NCCN) guidelines for Central Nervous System (CNS) Cancers mention in the Discussion Section that brachytherapy is one of several treatment options used by radiation oncologists. (16) However, the terms GliaSite, intracavitary, or balloon (related to CNS cancers) are not mentioned in these guidelines.

References:

  1. Chino K, Silvain D, Grace A et al. Feasibility and safety of outpatient brachytherapy in 37 patients with brain tumors using the GliaSite Radiation Therapy System. Med Phys 2008; 35(7):3383-8.
  2. Johannesen TB, Watne K, Lote K et al. Intracavity fractionated balloon brachytherapy in glioblastoma. Acta Neurochir (Wien) 1999; 141(2):127-33.
  3. Welsh J, Sanan A, Gabayan AJ et al. GliaSite brachytherapy boost as part of initial treatment of glioblastoma multiforme: a retrospective multi-institutional pilot study. Int J Radiat Oncol Biol Phys 2007; 68(1):159-65.
  4. Tatter SB, Shaw EG, Rosenblum ML et al. An inflatable balloon catheter and liquid 125I radiation source (GliaSite Radiation Therapy System) for treatment of recurrent malignant glioma: multicenter safety and feasibility trial. J Neurosurg 2003; 99(2):297-303.
  5. Chan TA, Weingart JD, Parisi M et al. Treatment of recurrent glioblastoma multiforme with GliaSite brachytherapy. Int J Radiat Oncol Biol Phys 2005; 62(4):1133-9.
  6. Payne JT, St Clair WH, Given CA, 2nd et al. Double balloon GliaSite in the management of recurrent glioblastoma multiforme. South Med J 2005; 98(9):957-8.
  7. Gabayan AJ, Green SB, Sanan A et al. GliaSite brachytherapy for treatment of recurrent malignant gliomas: a retrospective multi-institutional analysis. Neurosurgery 2006; 58(4):701-9; discussion 01-9.
  8. Gobitti C, Borsatti E, Arcicasa M et al. Treatment of recurrent high-grade gliomas with GliaSite brachytherapy: a prospective mono-institutional Italian experience. Tumori 2011; 97(5):614-9.
  9. Rogers LR, Rock JP, Sills AK et al. Results of a phase II trial of the GliaSite radiation therapy system for the treatment of newly diagnosed, resected single brain metastases. J Neurosurg 2006; 105(3):375-84.
  10. Matheus MG, Castillo M, Ewend M et al. CT and MR imaging after placement of the GliaSite radiation therapy system to treat brain tumor: initial experience. AJNR Am J Neuroradiol 2004; 25(7):1211-7.
  11. Wernicke AG, Sherr DL, Schwartz TH et al. The role of dose escalation with intracavitary brachytherapy in the treatment of localized CNS malignancies: outcomes and toxicities of a prospective study. Brachytherapy 2010; 9(1):91-9.
  12. Wernicke AG, Sherr DL, Schwartz TH et al. Feasibility and safety of GliaSite brachytherapy in treatment of CNS tumors following neurosurgical resection. J Cancer Res Ther 2010; 6(1):65-74.
  13. Barker FG, 2nd. Brain metastasis. J Neurosurg 2006; 105(3):371-2; discussion 72-4.
  14. Adkison JB, Thomadsen B, Howard SP. Systemic iodine 125 activity after GliaSite brachytherapy: safety considerations. Brachytherapy 2008; 7(1):43-6.
  15. Gerber DE, Grossman SA, Chan TA et al. Intracranial hemorrhage during GliaSite RTS manipulation in an anticoagulated patient. J Radiother Pract 2007; 6:53-57.
  16. National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology. Central Nervous System Cancers. (V.1.2013). Available online at: http://www.nccn.org/professionals/physician_gls/pdf/cns.pdf. Last accessed March 2013.

Codes

Number

Description

CPT    No specific CPT code 
ICD-9 Procedure  01.26 Insertion of catheter(s) into cranial cavity or tissue 
  01.27  Removal of catheter(s) from cranial cavity or tissue 
  92.20 Infusion of liquid brachytherapy radioisotope 
ICD-9 Diagnosis    Investigational for all diagnoses  
HCPCS  A9527 Iodine I-125 sodium iodide solution, therapeutic, per mci 
ICD-10-CM (effective 10/1/14)    Investigational for all diagnoses
  C71.0-C71.9 Malignant neoplasm of brain code range
ICD-10-PCS (effective 10/01/14)   ICD-10-PCS codes are only used for inpatient services.
  0WH103Z, 0WH133Z, 0WH143Z Surgical, insertion, infusion device, cranium, code by approach (open, percutaneous, percutaneous endoscopic)
  0WP1X3Z, 0WP103Z, 0WP133Z, 0WP143Z Surgical, removal, infusion device, cranium, code by approach (external, open, percutaneous, percutaneous endoscopic)
  3E0Q3HZ Administration of liquid brachytherapy radioisotope, percutaneous
  3E0Q7HZ Administration of liquid brachytherapy radioisotope, via natural or artificial opening

 


 

Index

Brachytherapy, Brain, Intracavitary
GliaSite

 


 

Policy History

Date Action Reason
02/15/07 Add to Therapy section New policy
12/11/08 Replace policy  Policy updated with literature search through October 2008. Reference numbers 10-14 added. No change to policy statement 
04/08/10 Replace policy Policy updated with literature search through February 2010; references 1, 10, 13 added, reference 14 updated. Rationale extensively revised. Minor wording changes to the policy statements; however, the intent of the statements remains unchanged
4/14/11 Replace policy Policy updated with literature search through February 2011; reference 14 added and reference 15 updated; policy statement unchanged, remains investigational
04/12/12 Replace policy Policy updated with literature search through February 2012; Rationale section reorganized; reference 8 added; policy statement unchanged.
04/11/13 Replace policy
Policy updated with literature search through February 2013; reference 16 updated; policy statements unchanged.