|Mature results of a randomized trial comparing two fractionation schedules of high dose rate endoluminal brachytherapy for the treatment of endobronchial tumors.|
|Jump to Full Text|
|PMID: 23289530 Owner: NLM Status: Publisher|
|ABSTRACT: Purpose: To determine the efficacy of high dose rate endobronchial brachytherapy (HDR-BT) for the treatment of centrally located lung tumors, two different fractionation schedules were compared regarding local tumor response, side effects and survival. Mature retrospective results with longer follow-up and more patients were analyzed. Initial results were published by Huber et al. in 1995.Methods and materials: 142 patients with advanced, centrally located malignant tumors with preferential endoluminal growth were randomized to receive 4 fractions of 3.8 Gy (time interval: 1 week, n = 60, group I) or 2 fractions of 7.2 Gy (time interval: 3 weeks, n = 82, group II) endobronchial HDR-BT.Age, gender, tumor stage, Karnofsky Performance Score and histology were equally distributed between both groups. RESULTS: Local tumor response with 2 fractions of 7.2 Gy was significantly higher as compared to 4 fractions of 3.8 Gy (median 12 vs. 6 weeks; p <= 0.015). Median survival was similar in both groups (19 weeks in the 4 fractions group vs. 18 weeks in the 2 fractions group). Fatal hemoptysis was less frequent following irradiation with 2 x 7.2 Gy than with 4 x 3.8 Gy, although the difference did not achieve statistical significance (12.2% vs. 18.3%, respectively. p = 0,345). Patients presenting with squamous cell carcinoma were at higher risk of bleeding compared to other histology (21.9% vs. 9%, p = 0,035).Multivariate analysis with regard to overall survival, revealed histology (p = 0.02), Karnofsky Performance Score (p < 0.0001) and response to therapy (p < 0.0001) as significant prognostic factors. For patients showing complete response the median survival was 57 weeks, while for patients with progressive disease median survival time was 8 weeks, p < 0.0001.The KPS at the start of the treatment was significantly correlated with survival. Patients presenting with a KPS <= 60 at the start had a significantly (p = 0,032) shorter survival time (10 weeks) than patients with a KPS > 60 (29 weeks).Moreover, the Karnofsky Performance Score of most patients improved during therapy (p = 0,001), suggesting successful palliation of cancer associated symptoms.Multivariate analysis with regard to local tumor control found no significant factors. CONCLUSION: Endobronchial HDR-BT is an effective local treatment for advanced centrally located malignant tumors with endoluminal tumor growth. Local tumor response was significantly higher after HDR-BT with 2 x 7.2 Gy.|
|Olivier M Niemoeller; Barbara Pöllinger; Maximilian Niyazi; Stefanie Corradini; Farkhad Manapov; Claus Belka; Rudolf M Huber|
|Type: JOURNAL ARTICLE Date: 2013-1-7|
|Title: Radiation oncology (London, England) Volume: 8 ISSN: 1748-717X ISO Abbreviation: Radiat Oncol Publication Date: 2013 Jan|
|Created Date: 2013-1-7 Completed Date: - Revised Date: -|
Medline Journal Info:
|Nlm Unique ID: 101265111 Medline TA: Radiat Oncol Country: -|
|Languages: ENG Pagination: 8 Citation Subset: -|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Radiat Oncol
Journal ID (iso-abbrev): Radiat Oncol
Publisher: BioMed Central
Copyright ©2013 Niemoeller et al; licensee BioMed Central Ltd.
Received Day: 29 Month: 5 Year: 2012
Accepted Day: 8 Month: 12 Year: 2012
collection publication date: Year: 2013
Electronic publication date: Day: 7 Month: 1 Year: 2013
Volume: 8First Page: 8 Last Page: 8
PubMed Id: 23289530
Publisher Id: 1748-717X-8-8
|Mature results of a randomized trial comparing two fractionation schedules of high dose rate endoluminal brachytherapy for the treatment of endobronchial tumors|
|Olivier M Niemoeller1||Email: firstname.lastname@example.org|
|Barbara Pöllinger1||Email: email@example.com|
|Maximilian Niyazi1||Email: firstname.lastname@example.org|
|Stefanie Corradini1||Email: Stefanie.Corradini@gmail.com|
|Farkhad Manapov1||Email: Farkhad.Manapov@med.uni-muenchen.de|
|Claus Belka1||Email: Claus.Belka@med.uni-muenchen.de|
|Rudolf M Huber2||Email: Huber@med.uni-muenchen.de|
1Department of Radiotherapy and Radiation Oncology, Ludwig-Maximilians University Munich, Marchioninistr. 15, 81377, Munich, Germany
2Division of Respiratory Medicine and Thoracic Oncology, Ludwig-Maximilians University Munich, Munich, Germany
Lung cancer is the leading cause of cancer associated deaths in the United States and Europe [1,2] with the majority of patients presenting with metastatic disease . Although substantial improvements in terms of survival time and quality of life have been achieved over the last decades [4,5], palliation of local and systemic cancer associated symptoms remains one main objective in the treatment of these patients. Local symptoms including dyspnea due to airway obstruction, cough and hemoptysis respond to chemotherapy  and external beam radiotherapy . Nonetheless, in a substantial number of patients, local symptoms may not be treated sufficiently  with more than 50% of the patients still suffering from cough, dyspnea and hemoptysis  stressing the need for further therapeutic strategies.
Although randomized data demonstrated a more sustained palliative effect of external beam radiotherapy (EBRT) when compared to a single dose brachytherapy, this was achieved at the expense of more acute side effects in the EBRT group and a substantially longer treatment time (10 – 12 days for EBRT versus a single treatment session for brachytherapy) .
Thus, especially in patients with limited prognosis presenting with local symptoms, high dose rate brachytherapy (HDR-BT) offers a number of advantages including short treatment time, a relatively fast onset of treatment response and less acute side effects, probably by limiting irradiated volumes of normal tissue.
Brachytherapy has also been proven to be clinically useful in order to prolong the effect of laser recanalization and prevent stent obstruction by tumor overgrowth .
With curative intent, brachytherapy has been utilized with some success as a boost to conventional external beam radiotherapy [19,20] or as definitive treatment for stage I lung cancer . However, in some series with longer follow up, relatively high rates of bronchial obstruction and fatal bleedings had been observed [19,21,22]. One non-randomized study compared different radiation doses (single dose of 20 Gy or 15 Gy at 1 cm from the central axis of the radiation source). In this study, multivariate analysis identified high single dose as a risk factor for fatal hemoptysis .
Although the effectiveness of HDR-BT in a palliative context is proven, no randomized data were available concerning the questions of optimal treatment dose and fractionation. Therefore we initiated a prospective randomized trial comparing two fractionation schedules in palliative lung cancer treatment. Interim results of this study obtained up to November 1993 were presented in 1995 . Here we present retrospective a analysis with more patients and longer follow-up.
After receiving informed consent, one hundred and forty two patients were included in the trial. Patients were eligible when the following criteria were met: Histologically or cytologically proven malignant lung tumor, tumor localization affecting the trachea, the main or lobar bronchi with a substantial occlusion of the lumen as determined by bronchoscopic examination, exclusion of other treatment options such as surgery, external beam radiotherapy, or chemotherapy, no concurrent tumor treatment. Randomization was done by a flipping coin procedure. There was no selection of the patients regarding age and gender, histological findings, tumor stage, or Karnofsky Performance Status (KPS). The study was approved by the local ethics committee and followed procedures were in accordance with the Helsinki declaration 1975 as revised in 1983.
Group I received a total dose of 15.2 Gy, delivered in 4 fractions of 3.8 Gy at 1 cm from the source axis at weekly intervals. Group II received a total dose of 14.4 Gy in two fractions of 7.2 Gy at 1 cm from the source axis with a time interval of three weeks. The dose concept was chosen in the early 1990s according to personal experience of therapists, which from a modern point of view seems somewhat old-fashioned. Brachytherapy was mainly carried out on an outpatient basis. Bronchoscopy was performed with the patient receiving topical anesthesia to determine the field intended for treatment. The treatment area was marked externally by fluoroscopy depending on the endoluminal tumor extension. Subsequently a guidewire was placed through the instrumentation channel of the endoscope. After removal of the bronchoscope, a shortened gastric tube with an external diameter of 0.5 mm was inserted via Seldinger technique over a guidewire and placed along side of the tumor region. The irradiation applicator was placed into the tube and taped to the tip of the nose to prevent dislocation. For brachytherapy a 192Ir HDR remote afterloading unit (Gammamed IIi, Isotopentechnik Dr. Sauerwein, Haan, Germany) was used.
Dose was calculated using the Plato TPS program. The treatment length was determined by bronchoscopy according to the endoluminal tumor extension including a safety margin of 10 mm. The dose was prescribed to 10 mm distance from the source axis.
Prior to randomization, the following baseline tests were performed: Routine blood chemistry, lung function tests, fiberoptic bronchoscopy, plain chest radiographs and computed tomographic scans. All patients were staged according to the international staging system for lung cancer as recommended by the American Joint Committee on Lung Cancer in 1988. Histologic classification was done following the guidelines of the World Health Organization . Karnofsky Performance Score was registered at the beginning and at the end of endoluminal irradiation.
Three months after brachytherapy a bronchoscopic control examination and a chest radiograph were performed to evaluate local control and tumor response. Local intraluminal tumor response as determined by bronchoscopy was defined as follows:
Tumor recurrence was characterized as intraluminal tumor disappearance followed by subsequent re-growth; tumor progression was defined as intraluminal persistence and further growth. No change was defined as persistent intraluminal tumor.
Complete remission was defined as no evidence of intraluminal tumor; partial response was defined as more than 25% tumor reduction. If complete remission, partial remission or no change was achieved, the response was rated as local control. The duration of local control was defined as time to progression judged by bronchoscopy. In case of a treatment failure during the follow up period an additional course of brachytherapy was allowed by the protocol.
Follow up was performed at regular intervals: The patients participated at the follow up study at defined intervals of three months. Fatal hemoptysis was defined as massive bleeding from the tracheo-bronchial tree leading to immediate death. A local intrathoracic problem was encountered when complications such as airway occlusion, pneumonia, or intrapulmonary metastasis were the main cause of death. Systemic complications were defined as distant metastasis causing death. Other causes were tumor unrelated disease or unknown reasons.
Survival time was considered the main endpoint. Assessment of local control as judged by bronchoscopy provided a second endpoint. The KPS was used to document the acute side-effect of brachytherapy or progression of disease.
All patients were analyzed on an intention-to-treat basis. Differences between both groups were considered significant with a p-value of less than 0.05. Survival plots were created using the procedure of Kaplan and Meier . Testing differences in survival time was done with the log rank test. All statistical analysis was calculated with the Statistical Package for Social Science (SPSS/PC for Windows 10.0).
142 patients were included in this study: 60 in group I (4 × 3.8 Gy) and 82 in group II (2 × 7.2 Gy). The imbalance in patient numbers results from a stop in randomization and consecutive patients were treated in group II. However, in retrospect it was not possible to identify the exact time-point at which the randomization was stopped. The baseline characteristics are shown in Table 1.
Group I consisted of 49 (81.7%) men and 11 (18.3%) women. Group II consisted of 53 (67.1%) men and 27 (32.9%) women. Median age was 64 years in group I and 65 years in group II. Most of the patients had advanced tumor stages. Only 21.1% in group I and 17.5% in group II had tumor stages below IIIB. In both groups more than 50% of the patients suffered from metastatic disease. The largest histologic subtype in both groups was squamous cell carcinoma (53.4% and 40.2%), followed by adeno carcinoma (17.2% and 26.8%).
Merely all patients were heavily pretreated. Most patients had various pre-treatments (97.4% in group I and 87.1% in group II), with a substantial number of patients having already received an external beam radiotherapy (41.2% in group I and 35.6% in group II) and a Nd-YAG laser therapy (33.3% in group I and 38.8% in group II). More than 45% in both groups underwent different treatment combinations.
A median KPS of 60 in both groups at study-begin illustrates the poor condition of the patients. After treatment the median KPS increased up to 70 (p = 0.005). This may indicate that brachytherapy causes little discomfort for the patients and delivers a good treatment option, especially in a palliative situation. Tumor localization was similar in both groups with a preference of the right bronchial system. The total irradiation dose was almost similar in both groups. 30% of the patients did not complete the intended treatment. Two patients (3.3%) in group I and 6 (7.3%) in group II received more than the initially intended dose due to tumor persistence.
The rates of local tumor response are shown in Table 2.
Local tumor control confirmed by bronchoscopy was significantly higher in group II compared to group I (p = 0.015). The mean time of local control in group I was 11 weeks whereas in group II it was 37 weeks (Figure 1). The duration of local control was defined as time from the last treatment to progression judged by bronchoscopy.
Analysis of the histological subgroups revealed that patients with squamous cell carcinoma in group II (n = 30/82) had a statistically significant (p = 0.024) better local control (median local control 28 weeks versus 8 weeks) than in group I (n = 26/60) (Figure 2). However, the improvement in local tumor control in this subgroup did not translate into a statistically significant survival benefit (median survival 19 weeks for group II versus 14 weeks for group I, p = 0.469).
Patients with small cell lung cancer in group II (n = 9/82) also had a statistically significant (p = 0.028) better local control than the patients in group I (n = 6/60). The other histological subgroups did not show a significant difference in local tumor control comparing group I and II.
One-year survival rates were 11.4% in group I and 21.1% in group II (median follow up of 20 weeks; range 1 to 251 weeks). Median survival in group I was 19 weeks, whereas in group II median survival was 18 weeks (p = n.s.) (Figure 3).
Adherence to treatment was similar in both groups. In group I 70 percent of the patients received the full dose, in group II 69.5 percent received the intended dose.
The KPS at the start of the treatment was significantly correlated with survival, with patients presenting with a KPS ≤ 60 at the start had a significantly (p = 0.03) shorter median survival time (10 weeks) than patients with a KPS > 60 (29 weeks) (Figure 4).
In both groups one third of the patients were dead after a follow up time of 12 weeks in group I and 9 weeks in group II. The underlying reasons were: Fatal hemoptysis which occurred in 11 patients (18.3%) in group I and in 10 patients in group II (12.2%). Patients with squamous cell carcinoma had a significantly higher risk of fatal hemoptysis compared to patients with other histological subtypes (p = 0,035).
8 patients in group I (13.3%) and 7 in group II (8.5%) died not related to tumor progression. Death in group I was caused by local problems in 12 patients (20%) and 27 patients in group II (32.9%). Causes of death were unknown in 9 patients in both groups respectively (15% vs. 12.2%) (Table 3).
Our data confirm former studies on high dose rate endobronchial brachytherapy (HDR-BT). We showed that endobronchial brachytherapy is an effective and safe therapeutic option in heavily pretreated patients with limited prognosis and low performance score. For patients with prior radiotherapy and limited prognosis HDR-BT offers a quick palliation of local symptoms, which is reflected in improved performance score.
Initially published results from the first 93 patients found no difference in either overall survival or local control with the two fractionation regimes . The present analysis including 142 patients shows that better local control rates are achieved when using 2 fractions of 7.2 Gy compared to 4 fractions of 3.8 Gy. Furthermore, local remission time and consequently symptom relief was significantly better using 2 fractions of 7.2 Gy. One explanation for this phenomenon might be a quicker development of clinical effects due to the application of a higher irradiation dose per fraction. In addition, this regime is less invasive and probably more cost-effective - although this subject was not within the scope of the study. However, in the context of an advanced systemic disease, the improved rates of local control following irradiation with 2 fractions of 7.2 Gy did not translate into a survival benefit.
Concerning the weaknesses of this study, it must be stated that a weakness of this analysis is the fact, that in retrospect it was not clear when the randomization was stopped, which might have biased the results. Nevertheless, since the mature results are in accord with the initial results the authors believe that the results are valid.
Moreover, since randomization was done by a flipping coin procedure and no selection by known risk factors was preformed, the results might be biased.
Concerning the limitations of endoluminal brachytherapy, one must consider that although this technique provides an important option for the treatment of tumor-derived airway occlusions, the effects of brachytherapy are delayed in time so that HDR-BT is not suitable when immediate symptom elimination is necessary.
The data presented here confirm that the KPS is an important prognostic factor. Patients with a KPS < 60 had a significant shorter survival time. Moreover, the KPS improved after treatment. This might indicate an effective palliation of local symptoms and a lack of severe acute side effects.
In summary, HDR-BT provides an excellent treatment option for patients suffering from tumor-associated airway obstruction. Using two fractions with 7.2 Gy at 10 mm from the source axis provides superior local control in a randomized comparison with four fractions of 3.8 Gy. Thus, this regimen should be used for palliative radiotherapy in patients with limited prognosis presenting with local symptoms.
Supported by a grant of the Wilhelm-Sander-Foundation No.: 87.015.1 and 87.015.2.
The authors declare that they have no competing interests.
OMN wrote the manuscript, BP acquired the data, MN did the statistics, SC did the statistics and provided the figures, FM contributed in data acquisition, CB developed the Concept, RMH did the acquisition of data and developed the concept. All authors read and approved the final manuscript.
|Jemal A,Siegel R,Ward E,Hao YP,Xu JQ,Murray T,Thun MJ,Cancer statistics, 2008CA Cancer J ClinYear: 200858719610.3322/CA.2007.001018287387|
|Goeckenjan G,Sitter H,Thomas M,Branscheid D,Flentje M,Griesinger F,Niederle N,Stuschke M,Blum T,Deppermann KM,et al. Prevention, diagnosis, therapy, and follow-up of lung cancerPneumologieYear: 201064Suppl 2e1e16420217630|
|de Jong WK,Schaapveld M,Blaauwgeers JLG,Groen HJM,Pulmonary tumours in the Netherlands: focus on temporal trends in histology and stage and on rare tumoursThoraxYear: 2008631096110210.1136/thx.2007.09506718678702|
|Non-small Cell Lung Cancer Collaborative GChemotherapy in non-small cell lung cancer: a meta-analysis using updated data on individual patients from 52 randomised clinical trialsBr Med JYear: 19953118999097580546|
|Spiro SG,Rudd RM,Souhami RL,Brown J,Fairlamb DJ,Gower NH,Maslove L,Milroy R,Napp V,Parmar MKB,et al. Chemotherapy versus supportive care in advanced non-small cell lung cancer: improved survival without detriment to quality of lifeThoraxYear: 20045982883610.1136/thx.2003.02016415454647|
|Roszkowski K,Pluzanska A,Krzakowski M,Smith AP,Saigi E,Aasebo U,Parisi A,Tran NP,Olivares R,Berille J,A multicenter, randomized, phase III study of docetaxel plus best supportive care versus best supportive care in chemotherapy-naive patients with metastatic or non-resectable localized non-small cell lung cancer (NSCLC)Lung CancerYear: 20002714515710.1016/S0169-5002(00)00094-510699688|
|Langendijk JA,Aaronson NK,de Jong JMA,ten Velde GPM,Muller MJ,Lamers RJ,Slotman BJ,Wouters EFM,Prospective study on quality of life before and after radical radiotherapy in non-small-cell lung cancerJ Clin OncolYear: 2001192123213311304764|
|Hanna N,Shepherd FA,Fossella FV,Pereira JR,De Marinis F,von Pawel J,Gatzemeier U,Tsao TCY,Pless M,Muller T,et al. Randomized phase III trial of pemetrexed versus docetaxel in patients with non-small-cell lung cancer previously treated with chemotherapyJ Clin OncolYear: 2004221589159710.1200/JCO.2004.08.16315117980|
|Speiser B,Spratling L,Intermediate dose-rate remote afterloading brachytherapy for intraluminal control of bronchogenic-carcinomaInt J Radiat Oncol Biol PhysYear: 1990181443144810.1016/0360-3016(90)90320-J1695215|
|Mehta M,Shahabi S,Jarjour N,Steinmetz M,Kubsad S,Effect of endobronchial radiation-therapy on malignant bronchial obstructionChestYear: 19909766266510.1378/chest.97.3.6622306968|
|Gauwitz M,Ellerbroek N,Komaki R,Putnam JB,Ryan MB,Decaro L,Davis M,Cundiff J,High-dose endobronchial irradiation in recurrent Bronchogenic-carcinomaInt J Radiat Oncol Biol PhysYear: 19922339740010.1016/0360-3016(92)90759-B1587762|
|Kubaszewska M,Skowronek J,Chichel A,Kanikowski M,The use of high dose rate endobronchial brachytherapy to palliate symptomatic recurrence of previously irriadiated lung cancerNeoplasmaYear: 20085523924518348661|
|Taulelle M,Chauvet B,Vincent P,Felix-Faure C,Buciarelli B,Garcia R,Brewer Y,Reboul F,High dose rate endobronchial brachytherapy: results and complications in 189 patientsEur Respir JYear: 19981116216810.1183/09031936.98.110101629543287|
|Kelly JF,Delclos ME,Morice RC,Huaringa A,Allen PK,Komaki R,High-dose-rate endobronchial brachytherapy effectively palliates symptoms due to airway tumors: The 10-year M, D. Anderson Cancer Center experienceInt J Radiat Oncol Biol PhysYear: 20004869770210.1016/S0360-3016(00)00693-311020566|
|Anacak Y,Mogulkoc N,Ozkok S,Goksel T,Haydaroglu A,Bayindir U,High dose rate endobronchial brachytherapy in combination with external beam radiotherapy for stage III non-small cell lung cancerLung CancerYear: 20013425325910.1016/S0169-5002(01)00249-511679184|
|Macha HN,Wahlers B,Reichle C,Vonzwehl D,Endobronchial radiation-therapy for obstructing malignancies - 10 years experience with ir-192 high-dose radiation brachytherapy afterloading technique in 365 patientsLungYear: 19951732712807564485|
|Stout R,Barber P,Burt P,Hopwood P,Swindell R,Hodgetts J,Lomax L,Clinical and quality of life outcomes in the first United Kingdom randomized trial of endobronchial brachytherapy (intraluminal radiotherapy) vs. external beam radiotherapy in the palliative treatment of inoperable non-small cell lung cancerRadiother OncolYear: 20005632332710.1016/S0167-8140(00)00252-810974381|
|Chella A,Ambrogi MC,Ribechini A,Mussi A,Fabrini MG,Silvano G,Cionini L,Angeletti CA,Combined Nd-YAG laser/HDR brachytherapy versus Nd-YAG laser only in malignant central airway involvement: a prospective randomized studyLung CancerYear: 20002716917510.1016/S0169-5002(99)00102-610699690|
|Aygun C,Weiner S,Scariato A,Spearman D,Stark L,Treatment of non-small-cell lung-cancer with external beam radiotherapy and high-dose rate brachytherapyInt J Radiat Oncol Biol PhysYear: 19922312713210.1016/0360-3016(92)90551-R1315311|
|Huber RM,Fischer R,Hautmann H,Pöllinger B,Häussinger K,Wendt T,Does additional brachytherapy improve the effect of external irradiation? A prospective, randomized study in central lung tumorsInt J Radiat Oncol Biol PhysYear: 19973853354010.1016/S0360-3016(97)00008-49231677|
|Perol M,Caliandro R,Pommier P,Malet C,Montbarbon X,Carrie C,Ardiet JM,Curative irradiation of limited endobronchial carcinomas with high-dose rate brachytherapy - Results of a pilot studyChestYear: 19971111417142310.1378/chest.111.5.14179149603|
|Gollins SW,Ryder WDJ,Burt PA,Barber PV,Stout R,Massive haemoptysis death and other morbidity associated with high dose rate intraluminal radiotherapy for carcinoma of the bronchusRadiother OncolYear: 19963910511610.1016/0167-8140(96)01731-88735477|
|Huber RM,Fischer R,Hautmann H,Pöllinger B,Wendt T,Müller-Wening D,Häussinger K,Palliative endobronchial brachytherapy for central lung-tumors - a prospective, randomized comparison of 2 fractionation schedulesChestYear: 199510746347010.1378/chest.107.2.4637531132|
|The world-health-organization histological typing of lung-tumorsAm J Clin PatholYear: 1982771231367064914|
|Kaplan EL,Meier P,Nonparametric-estimation from incomplete observationsJ Am Stat AssocYear: 19585345748110.1080/01621459.1958.10501452|
|Group I (n = 60)||Group II (n = 82)|
|Median Age (range)
|Male n = 49
||n = 53 (67.1%)
|Female n = 11
||n = 27 (32.9%)
|Squamous Cell Carcinoma
|Oat Cell Carcinoma
|Pre-Treatment: (more than 100% because of different treatment combinations)
|Proximal localization of the irradiation probe
|Right main bronchus
|Left main bronchus
|Right distal bronchus
|Left distal bronchus||7.1%||2.6%|
Tumor Response in Group I and II at the time of the first control-bronchoscopy
Group I (4 × 3.8 Gy)
Group II (2 × 7.2 Gy)
|(n = 60)||(n = 82)|
Causes of death
|Group I (4 × 3.8 Gy)||Group II (2 × 7.2 Gy)|
|Other reason than tumor progression
Keywords: Endobronchial radiotherapy, High dose rate brachytherapy, Lung cancer, Re-irradiation.
Previous Document: T'ai Chi as Exercise Among Middle-Aged and Elderly Chinese in Urban China.
Next Document: Energetic basis of uncoupling folding from binding for an intrinsically disordered protein.