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Early evaluation predicts pain relief of irradiated bone metastases: a single-center prospective study



Radiation therapy is a well-recognized, effective modality used for palliative care. Most studies completed to date have endpoints of one month or greater after treatment completion. This study analyzed the response rates at different time points during the first month after treatment.


From May 2010 to November 2011, 61 patients treated for 74 metastases were included in the study. The end points were defined as the completion of treatment (CT) and d8, d15 and d30 after the completion of treatment. The response rate was measured by the worst pain in the last 24 hours and the administered opioid dose. Patient assessment was performed during consultations and phone appointments.


The overall response rate significantly improved from the CT (38%) to d8 (53.8%), d15 (53.8%) and d30 (57.1%) (respectively p < 0.001; p < 0.001 and p = 0.001). The improvement peaked at d8. Patients responding to the treatment at d8 had a significative longer pain relapse free survival (PRFS) compared to patients not responding (3.38 weeks vs 0.3 weeks; p < 0.001). From the beginning of treatment to the CT and at d8 , d15 and d30, oral morphine equivalent dose (OMED) did not significantly differ. However, the pain decrease did not result in a performance status improvement, which declined over time (p < 0.001).


Radiation therapy is an efficient treatment method for providing pain relief. This relief peaked at d8 after treatment, and the response at d8 is predictive of the response at 4 weeks. Pain management alone is not enough to improve performance status; further studies are needed to evaluate a more global supportive care approach.

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Approximately 50% of patients with cancer present metastases at the initial presentation or at relapse. Bone is one of the most frequent metastasis locations, particularly for lung, breast, and prostate cancers. Pain is the most common and debilitating symptom of bone metastases. Pain alters patient quality of life and requires specific support. This support includes motor function improvement and local or systemic treatment. Treatment may consist of the concomitant or alternate administration of analgesics, chemotherapy, hormone therapy, bisphosphonates, surgery, interventional radiology, and radiotherapy.

External beam irradiation for painful bone metastases has been well established by many prospective trials and can lead to pain relief and/or reduce analgesic consumption. Several radiation treatment schedules with similar effectiveness have been described. The most used schedules deliver 30 Gy in 10 fractions of 3 Gy, 20 Gy in 5 fractions of 4 Gy or a single fraction of 8 Gy [17]. An updated meta-analysis did not find any differences in the overall response rates between multi- and single fractionation (61% and 60%, respectively) [8]. Stereotactic beam radiation therapy (SBRT) and intensity-modulated radiotherapy (IMRT) have proved their effectiveness in spinal bone metastasis irradiation and re-irradiation [912]. A recent review showed that local control was achieved in 87% of cases [13].

The response to irradiation has been evaluated using many different types of measure. Visual analogue scales, a numeric scale, a Brief Pain Inventory, the dose of analgesics and the requirement for re-irradiation are the most frequently used [14]. Furthermore, the follow-up evaluation period after the completion of radiotherapy is variable in all trials and retrospective studies. Currently, evaluations at one or two months after irradiation completion are used to predict the definitive response to radiotherapy. However, this waiting time can be considered as too long to efficiently manage painful metastasis using re-irradiation, particularly as the life expectancy of these patients is short.

In this study, we report the response rate at the end of treatment and one, two and four weeks after treatment to determine whether an earlier evaluation could predict a definitive response.


From May 2010 to October 2011, patients referred to the radiation department of the Regional Cancer institute Paul Strauss for painful bone metastases were eligible to participate in this study examining the response after irradiation. The inclusion criteria were age above 18, ability to understand and speak French and consent to participate to the study. This study was approved by our institutional review board (committee against pain CLUD). Patients who underwent previous surgery, cementoplasty, or in-field irradiation and remained in pain were also included. Clinical evaluations were performed at the first radiotherapy consultation (beginning of treatment, BT) and at the completion of treatment (CT). Patients provided informed consent. A visual analogue scale (VAS) strip was given to each patient to evaluate their pain at home after being instructed on how to use it. On days 8, 15 and 30 after the CT, evaluations were performed during a scheduled phone appointment. The interviewer (PT) used a home survey to obtain the patient information.

The information collected at the first consultation included age, gender, primary cancer location, pathology, painful bone metastasis location, performance status, steroid treatment, analgesic morphine taken in the last 24 hours converted to the oral morphine equivalent dose (OMED) and local treatments received previously [15]. On d8, d15 and d30, OMED, performance status, and the minimum, mean and maximal pain evaluations in the past 24 hours (assessed using the VAS) were reported. The adverse effects of radiation therapy were reported according to the CTCAE v4. Patients who did not answer the phone were considered missing but were not excluded from the study.

The radiotherapy response rates were evaluated using the international bone metastases consensus group (IBMCG) criteria (Table 1).

Table 1 The response rate to radiotherapy according to the IBMCG criteria

The treatment was performed using linear accelerators with 6 MV or 15 MV photon beams. The TomoTherapy Hi-ART and Novalis TX systems were used for IMRT and SBRT treatment planning. The time period between the first consultation and the first irradiation session did not exceed 2 weeks.

Statistical analysis

The response rates at the different end points were compared for each patient: i) between the BT and CT, BT- d8, BT-d15 and BT-d30, ii) between the CT and d8, CT- d15 and CT-d30 iii) between d8- d15 and d8-d30, iv) between d15 and d30. Only patients with an available response rate at the compared end points were analyzed, and if the information was missing, the patient was excluded from the statistical analysis at the corresponding end point. Responders were patients with a complete response (CR) or a partial response (PR); patients with stable disease (SD), progressive disease (PD) and undetermined responses (UR) were considered as non-responders. The distributions of the Karnofsky performance status (KPS) (< 70% and ≥70%) and World Health Organisation performance status (WHO PS) (<2 and ≥ 2) at each evaluation were analyzed by the χ2 test. The nonparametric Wilcoxon test was used to compare repeated measures of pain score and OMED. A pain relapse free survival (PRFS) was calculated for the patients responding at every end points from the CT to d30 (range from 0 to 4 weeks). PRFS was analysed using a Kaplan Meyer method. p <0.05 was considered significant. Data were analyzed using SPSS version 20 (IBM Software).


Between May 2010 and November 2011, 61 patients were enrolled in the study. The general characteristics of the patients are summarized in Table 2. These 61 patients were treated for 74 metastatic locations: 31 were spinal (42%), 21 were pelvic (28%), 10 were long bones (13%) 8 were scapula (11%), 3 were rib, and 1 was mandibular. Forty-nine patients were treated for one metastatic location (80%), 11 for two (18%) and 1 patient for three.

Table 2 General patient characteristics before irradiation

Forty-nine metastatic sites were not treated previously (66%). Twenty five metastases were treated before the present irradiation, within a minimum of one month. Ten metastases (14%) were operated on (decompressive, stabilization), 9 (12%) received cementoplasty, 5 (7%) were irradiated, and 1 patient underwent surgery and radiotherapy. The six patients who previously received irradiation presented metastases located in spine for four and in pelvis for two metastases. The irradiation schedules before re-irradiation were 8 Gy in a single fraction (one patient), 24 Gy in 6 fractions of 4 Gy (one patient), 30 Gy in 10 fractions of 3 Gy (two patients), and 36 Gy in 12 fractions of 3 Gy (two patients).

Concerning the current irradiation, 66 bone metastases (89%) were treated with 3D conformational radiotherapy. Seven spinal metastases (9.5%) were treated with SBRT (re-irradiation in 4 cases). One metastasis was treated with IMRT. For 62 treatments (91%), the dose schedules were 8 Gy in a single fraction, 20 Gy in 5 fractions of 4 Gy and 30 Gy in 10 fractions of 3 Gy. The SBRT dose was 23.31 Gy in 3 fractions of 7.77 Gy delivered on days 1, 3 and 5. Other fractionations were proposed in 5 patients.

All patients included completed the treatment, and an evaluation at the completion of treatment was performed in 50 patients (82%). On days 8, 15 and 30, evaluations were obtained from 39 (64%), 39 (64%), and 42 (69%) patients, respectively. The reasons for no reply included unreachable by phone, death or refusal to continue the study (Table 3). Patients not responding at d30 had a statistically significant worse WHO-PS (3 vs 2; p = 0.018), but age, gender, VAS and OMED weren’t statistically different. The response rate to the treatment, median worst pain, median WHO-PS, KPS and OMED are presented in Tables 4 and 5.

Table 3 The reasons for non-evaluation
Table 4 Response rates
Table 5 The intensity of the worst pain, OMED, performance status, and Karnofsky index at baseline, the CT, d8, d15 and d30 after radiotherapy treatment

Analysis of visual scale

Using the visual scale, the patients had a significant decrease in the median maximal pain from the BT to the CT from VAS 7 to VAS 5, respectively (p = 0.001). From the BT to d8, d15 and d30, the VAS decreased to 3 and remained statistically significant (p < 0.001 at each evaluation). There was no significant difference in the maximal VAS from the CT to d8, d15 or d30 (p = 0.115; p = 0.088; p = 0.072, respectively), from d8 to d15 or d30 (p = 0.441 and p = 0.393, respectively) or from d15 to d30 (p = 0.345).

Analysis of OMED

The OMED did not significantly differ between each interval of evaluation. The mean OMEDs at the BT, the CT, d8, d15 and d30 were 40 mg, 40 mg, 30 mg, 30 mg and 40 mg, respectively (p = 0.93 between BT and CT, p = 0.64, for CT-d8, p = 0.47 for CT-d15, p = 0.96 for CT-d30 and p = 0.96 for BT-d30).

Analysis of IBMCG

The overall response rates at CT, d8, d15 and d30 were 38%; 53.8%; 53.8% and 57.1% respectively. The CR rates at CT, d8, d15 and d30 were 8%, 10.3%, 15.3% and 16.7% respectively. Using the IBMCG criteria, there were significant improvements (CR, PR) from the CT to d8, d15 and d30 (p < 0.001; p < 0.001 and p = 0.001, respectively), from d8 to d15 and d30 (p < 0.001 and p = 0.001, respectively), and from d15 to d30 (p = 0.002). Univariate analysis using Kaplan Meyer method highlighted PRFS for patients having a response at d8 was significantly improved compared to patients not responding: respectively 3,38 weeks vs 0,3 weeks (p < 0,001). This result suggests response at d8 is predictive of response at d30.

Performance status (WHO PS and KPS)

Compared to the BT, WHO PS and KPS were significantly decreased at the CT, d8 and d30 (p < 0.001). However, at d15, the data showed a transitory improvement in WHO-PS and KPS (p < 0.001).

Irradiation side effects

The side effects of radiotherapy included dermatitis, nausea, vomiting, diarrhea and dysphagia in 11 patients (18%) at the CT, 9 (15%) patients at d8, 9 (15%) patients at d15 and 9 (15%) patients at d30 (Table 6). According to CTCAE v4, only one patient developed grade 3 toxicity at the CT and d8; the remaining patients experienced grade 2 or less toxicities. After d8, the toxicities were grade 2 or less.

Table 6 Radiation therapy side effects at different end points


Several consensus task forces have attempted to recommend tools or methods for following and evaluating patients with bone metastases [16, 17]. One of the recommendations was to assess pain at 2 months after the CT [18]. However, we believe that this amount of time is too long for patients in pain who may have a short life expectancy. Our study clearly showed that an evaluation at d8 is sufficient for proposing re-irradiation or another treatment for remaining painful metastases, as patients not responding at this end point have significantly lower PRFS. Another proposal was to perform re-irradiation at least one month after the previous irradiation. However, with new techniques, such as IMRT or SBRT, which can shield organs at risk (particularly the spinal cord), a higher efficient dose can be delivered, dramatically increasing the chance of controlling pain with a very low risk of complications.

This study showed phone evaluation’s feasibility to assess response to an antalgic irradiation, in order to be able to propose an adequate care of the pain. This method allows the assessment of patients at home, which is more comfortable and avoids travel. Phone evaluations can be performed by a radiation oncologist or a trained nurse. In 2004, a study assessing 830 patients by phone retrieved a higher percent of patients reachable by phone at 4 weeks (57%) after treatment completion with a steady decrease through 12 weeks (48%) [19]. Our results are comparable to that study, with 72% of patients reachable at the CT and 64-69% at d8, d15 and d30. As in a previously published series, the main cause of no reply was death or hospitalization [19].

In 2004, Chow and al. analyzed 580 patients’ response rates to radiation therapy using pain intensity scale and analgesic consumption [20]. In this study the overall response rates at 1, 2 and 4 weeks were 41%, 41% and 39% respectively. The CR rates at 1, 2 and 4 weeks were 32%, 28% and 26% respectively. In our study the overall response rates at 1,2 and 4 weeks were 38%, 53.8%, 53.8% and 57.1% respectively and CR at 1,2 and 4 weeks were 8%, 10.3%, 15.3%, and 16.7%. Our results are comparable to previously published results using the same evaluation method (IBMCG) [20] and time at evaluation (one month) [21].

Despite the improvement of the overall response to pain after radiation therapy, our study showed a worsening of the performance status. Patients had an altered performance status with a median WHO PS of 2 (0–4) at the BT. In several previous studies and trials, most patients had a WHO PS ≥ 2 [4, 5]. Unfortunately, patients with a very poor performance status at the BT, have a low probability of improving their performance status because many factors contribute to this status. However, one study showed that such patients with a short life expectancy may benefit from analgesic irradiation [22].

This study has some limitations: the population is mixed concerning metastatic localization, performance status, radiation therapy schedule, and radiation technique (RTC 3D or SBRT).


The prospective study demonstrated that radiation therapy is a quick and efficient treatment of bone metastasis pain. A phone evaluation of pain relief is feasible in practice. The evaluation of pain at d8 after the CT is predictive of pain relief thereafter. Thus, if needed, treatment decisions can be made earlier in the patient’s disease course. However, a good pain response is not strictly correlated to performance status.



Visual analogue scale


Beginning of treatment


Complete response


Completion of treatment


Karnofsky performance status


International bone metastases consensus group


Intensity-Modulated radiation therapy


Oral morphine equivalent dose


Progression disease


Partial response


Pain relapse free survival


Radiation treatment


Stable disease


Stereotactic beam radiation therapy


Undetermined response


World health organisation performance status.


  1. Bone Pain Trial Working Party BPTW: 8 Gy single fraction radiotherapy for the treatment of metastatic skeletal pain: randomised comparison with a multifraction schedule over 12 months of patient follow-up. Bone Pain Trial Working Party. Radiother Oncol. 1999, 52: 111-121. 10.1016/S0167-8140(99)00097-3.

    Article  Google Scholar 

  2. Jeremic B, Shibamoto Y, Acimovic L, Milicic B, Milisavljevic S, Nikolic N, Aleksandrovic J, Igrutinovic I: A randomized trial of three single-dose radiation therapy regimens in the treatment of metastatic bone pain. Int J Radiat Oncol Biol Phys. 1998, 42: 161-167.

    Article  CAS  PubMed  Google Scholar 

  3. Price P, Hoskin PJ, Easton D, Austin D, Palmer SG, Yarnold JR: Prospective randomised trial of single and multifraction radiotherapy schedules in the treatment of painful bony metastases. Radiother Oncol. 1986, 6: 247-255. 10.1016/S0167-8140(86)80191-8.

    Article  CAS  PubMed  Google Scholar 

  4. Steenland E, Leer JW, van Houwelingen H, Post WJ, van den Hout WB, Kievit J, de Haes H, Martijn H, Oei B, Vonk E: The effect of a single fraction compared to multiple fractions on painful bone metastases: a global analysis of the Dutch Bone Metastasis Study. Radiother Oncol. 1999, 52: 101-109. 10.1016/S0167-8140(99)00110-3.

    Article  CAS  PubMed  Google Scholar 

  5. Nielsen OS, Bentzen SM, Sandberg E, Gadeberg CC, Timothy AR: Randomized trial of single dose versus fractionated palliative radiotherapy of bone metastases. Radiother Oncol. 1998, 47: 233-240. 10.1016/S0167-8140(98)00011-5.

    Article  CAS  PubMed  Google Scholar 

  6. Sze WM, Shelley MD, Held I, Wilt TJ, Mason M: Palliation of metastatic bone pain: single fraction versus multifraction radiotherapy--a systematic review of the randomised trials. Clin Oncol (R Coll Radiol). 2003, 15: 345-352. 10.1016/S0936-6555(03)00113-4.

    Article  CAS  Google Scholar 

  7. Wu JS, Wong R, Johnston M, Bezjak A, Whelan T: Meta-analysis of dose-fractionation radiotherapy trials for the palliation of painful bone metastases. Int J Radiat Oncol Biol Phys. 2003, 55: 594-605. 10.1016/S0360-3016(02)04147-0.

    Article  PubMed  Google Scholar 

  8. Chow E, Zeng L, Salvo N, Dennis K, Tsao M, Lutz S: Update on the systematic review of palliative radiotherapy trials for bone metastases. Clin Oncol (R Coll Radiol). 2012, 24: 112-124. 10.1016/j.clon.2011.11.004.

    Article  CAS  Google Scholar 

  9. Ryu S, Fang Yin F, Rock J, Zhu J, Chu A, Kagan E, Rogers L, Ajlouni M, Rosenblum M, Kim JH: Image-guided and intensity-modulated radiosurgery for patients with spinal metastasis. Cancer. 2003, 97: 2013-2018. 10.1002/cncr.11296.

    Article  PubMed  Google Scholar 

  10. Chang BK, Timmerman RD: Stereotactic body radiation therapy: a comprehensive review. Am J Clin Oncol. 2007, 30: 637-644. 10.1097/COC.0b013e3180ca7cb1.

    Article  PubMed  Google Scholar 

  11. Gerszten PC, Burton SA, Ozhasoglu C, Welch WC: Radiosurgery for spinal metastases: clinical experience in 500 cases from a single institution. Spine (Phila Pa 1976). 2007, 32: 193-199. 10.1097/01.brs.0000251863.76595.a2.

    Article  Google Scholar 

  12. Gerszten PC, Mendel E, Yamada Y: Radiotherapy and radiosurgery for metastatic spine disease: what are the options, indications, and outcomes?. Spine (Phila Pa 1976). 2009, 34: S78-92. 10.1097/BRS.0b013e3181b8b6f5.

    Article  Google Scholar 

  13. Sahgal A, Larson DA, Chang EL: Stereotactic body radiosurgery for spinal metastases: a critical review. Int J Radiat Oncol Biol Phys. 2008, 71: 652-665. 10.1016/j.ijrobp.2008.02.060.

    Article  PubMed  Google Scholar 

  14. Cleeland CS, Ryan KM: Pain assessment: global use of the Brief Pain Inventory. Ann Acad Med Singapore. 1994, 23: 129-138.

    CAS  PubMed  Google Scholar 

  15. Svendsen K, Borchgrevink P, Fredheim O, Hamunen K, Mellbye A, Dale O: Choosing the unit of measurement counts: the use of oral morphine equivalents in studies of opioid consumption is a useful addition to defined daily doses. Palliat Med. 2011, 25: 725-732. 10.1177/0269216311398300.

    Article  CAS  PubMed  Google Scholar 

  16. Wu JS, Bezjak A, Chow E, Kirkbride P: Primary treatment endpoint following palliative radiotherapy for painful bone metastases: need for a consensus definition?. Clin Oncol. 2002, 14: 70-77. 10.1053/clon.2001.0012.

    Article  Google Scholar 

  17. Chow E, Hoskin P, Mitera G, Zeng L, Lutz S, Roos D, Hahn C, van der Linden Y, Hartsell W, Kumar E: Update of the international consensus on palliative radiotherapy endpoints for future clinical trials in bone metastases. Int J Radiat Oncol Biol Phys. 2012, 82: 1730-1737. 10.1016/j.ijrobp.2011.02.008.

    Article  PubMed  Google Scholar 

  18. Li KK, Hadi S, Kirou-Mauro A, Chow E: When should we define the response rates in the treatment of bone metastases by palliative radiotherapy?. Clin Oncol (R Coll Radiol). 2008, 20: 83-89. 10.1016/j.clon.2007.09.009.

    Article  CAS  Google Scholar 

  19. Chow E, Fung KW, Bradley N, Davis L, Holden L, Danjoux C: Review of telephone follow-up experience at the Rapid Response Radiotherapy Program. Support Care Cancer. 2005, 13: 549-553. 10.1007/s00520-004-0707-1.

    Article  PubMed  Google Scholar 

  20. Chow E, Holden L, Schueller T, Wong R, Hayter C, Hruby G, Szumacher E, Loblaw A, Danjoux C: A Comparison of Radiation Therapy Outcomes of Bone Metastases Employing International Consensus Endpoints and Traditional Endpoints. Support Cancer Ther. 2004, 1: 173-178. 10.3816/SCT.2004.n.009.

    Article  Google Scholar 

  21. Harris K, Li K, Flynn C, Chow E: Worst, average or current pain in the Brief Pain Inventory: which should be used to calculate the response to palliative radiotherapy in patients with bone metastases?. Clin Oncol (R Coll Radiol). 2007, 19: 523-527. 10.1016/j.clon.2007.04.007.

    Article  CAS  Google Scholar 

  22. Meeuse JJ, van der Linden YM, van Tienhoven G, Gans RO, Leer JW, Reyners AK: Efficacy of radiotherapy for painful bone metastases during the last 12 weeks of life: results from the Dutch Bone Metastasis Study. Cancer. 2010, 116: 2716-2725.

    PubMed  Google Scholar 

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Correspondence to Georges Noel.

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The authors declare no conflicts of interest.

Authors’ contribution

PT included patients, interviewed patients by phone, conducted statistical analysis, and drafted the manuscript. GN included patients, conceived of the study and participated in its design and coordination and helped to draft the manuscript. DA, MP, JBC, SG, CS included patients. All authors read and approved the final manuscript.

Pierre Truntzer and Georges Noel contributed equally to this work.

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Truntzer, P., Atlani, D., Pop, M. et al. Early evaluation predicts pain relief of irradiated bone metastases: a single-center prospective study. BMC Palliat Care 12, 12 (2013).

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