Cross-cultural adaptation and validation of the Chinese version of Toronto Extremity Salvage Score for patients with extremity sarcoma
© The Author(s) 2016
Received: 24 May 2016
Accepted: 12 July 2016
Published: 19 July 2016
As a widely used instrument for patients with extremity sarcoma, the Toronto Extremity Salvage Score (TESS) has never been cross-culturally adapted for Chinese population. The objective of our study was to investigate the comprehensibility, reliability and validity of the Chinese version of TESS for use in patients with extremity sarcoma.
A consensus version of the Chinese TESS was developed under the review of a committee according to international guidelines. 64 patients were recruited to complete the Chinese TESS, the Musculoskeletal Tumor Society (MSTS) Rating Scale, and the Quality of Life Questionnaire Core 30 (QLQ-C30). Reliability was assessed using the intra-class correlation coefficient (ICC) and Cronbach’s α. Validity was assessed with Pearson’s correlation between the similar domains of the two questionnaires.
The ICCs for the test–retest reliability was 0.932 for the upper extremity questionnaire and 0.893 for lower extremity questionnaire, respectively. The Cronbach’s α was 0.953 for the lower extremity questionnaire and 0.921 for the upper extremity questionnaire, respectively. Convergent validity of the TESS based on Pearson correlation coefficients indicated significantly moderate to high correlations between the TESS and the MSTS as well as the QLQ-C30, with r ranging from 0.535 to 0.782.
The Chinese TESS is a comprehensible, reliable, and valid instrument that can be utilized for future cross-cultural international studies of extremity sarcoma.
KeywordsTESS Chinese Extremity sarcoma Function
Sarcoma is a rare type of cancer that represents approximately 1 % of all newly diagnosed cancers (Borden et al. 2003). Due to the significant impact of extremity sarcoma surgery on the patients’ function, health related quality of life (HRQoL) is now recognized as an important outcome measure of the surgery (Hoffmann et al. 2006; Griesser et al. 2012; Ruggieri et al. 2011). Development of instruments to measure HRQoL is essential to determine patients’ perceived physical and mental health (Schreiber et al. 2006; Lopez-Guerra et al. 2011). To be noted, patients with sarcoma may have a significant heterogeneity regarding tumor type, reconstructive techniques and the extent of tissue excised during surgery. Therefore, it is important to develop an instrument that takes heterogeneity into account when measuring functional outcome. And a disease-specific measure rather than a generic measure is preferred for the proper assessment of physical function in patients with extremity sarcoma.
To date, several disease-specific questionnaires have already been developed to evaluate functional outcomes for patients undergoing surgery for extremity sarcomas (Davis et al. 1996; Enneking et al. 1993; Bekkering et al. 2009). Some examiner-dependent clinical measures such as range of motion and muscle strength or a combination of symptoms and mobility have been used. However, measures that reflect the patient’s perception seems more desirable in clinical practice. As a patient-completed questionnaire that takes into account the heterogeneity of sarcomas, the Toronto Extremity Salvage Score (TESS) was developed for assessing physical function of patients undergoing surgery for extremity sarcoma (Davis et al. 1996).
The TESS questionnaire is a disease-specific and self-administered questionnaire based on the definitions of disability, impairment, and handicap as documented by the World Health Organization (Davis et al. 1996). The content of the TESS includes the types of functional difficulties experienced by extremity sarcoma patients, such as body movement, mobility, self-care, and performing daily tasks. To date, several studies have reported the validation of the TESS in a Portuguese (Saraiva et al. 2008), Danish (Saebye et al. 2014), Korean (Kim et al. 2015) and Japanese version (Ogura et al. 2015), yielding good test–retest reliability and internal consistency. However, to the best of our knowledge, there is no study that addresses the application of TESS to patients from the Chinese population. Herein, this study was conducted to investigate the comprehensibility, reliability and validity of the Chinese version of TESS for use in patients with extremity sarcoma.
The protocol of recruitment of participants was approved by the ethics committee of the hospital. Patients who visited our clinic center between March 2011 and September 2014 were prospectively evaluated for the eligibility of recruitment in this study. The following inclusion criteria were used: (1) aged more than 18 years; (2) at least 1 year after curative surgery for histologically confirmed extremity sarcoma; (3) without local recurrence, distant metastasis or complications related to surgery. Finally, 64 patients including 35 male and 29 female participated in the study and gave their informed consent. Demographic data were collected from the medical records, including patients’ age, gender, location of the tumor, histological type, type of surgery and period of follow-up.
Translation and adaptation of the TESS
The translation and adaptation processes of the TESS were performed according to the guidelines used by previous literatures (Saraiva et al. 2008; Kim et al. 2015; Ogura et al. 2015). The English version of the TESS was translated into Chinese independently by three native Chinese bilingual translators who were familiar with the topic and the research concept. Subsequently, the two translators with the medical background analyzed and compared the three translations together with two senior musculoskeletal oncologists, and then combined them into one single translation. The consensus version was back translated into English independently by two bilingual translators who were kept blind to the procedures of the forward translation. All versions of the translation were analyzed by the expert committee, which was comprised of the 5 translators, one methodologist, and 2 orthopedic surgeons (X.L. and W.S.). The committee evaluated conceptual equivalence of all items and answers, and discrepancies between members were discussed. The pre-final version of the TESS was created after consensus was reached among the expert committee. In the pre-test step, 40 volunteers aged more than 18 years were recruited from the local community to test the pre-final Chinese version of the TESS. These volunteers were questioned about their understanding of the questionnaire items. Most of the items in the questionnaire could be correctly understood and answered by the volunteers. There was a high incidence of “not applicable” with regard to the question on sexual activity, which was therefore omitted from the questionnaire. After this process, the final version of the Chinese version of the TESS was developed. It consists of a lower extremity and an upper extremity version both with 29 questions. Each question is rated on 5-point scale, including “impossible to do,” “extremely difficult,” “moderately difficult,” “a little bit difficult,” and “not at all difficult”. The participant can select “not applicable” when the question is not a usual activity. The total score ranges from 0 to 100, with higher scores indicating better function.
Reliability and validity test of the TESS
All the patients were asked to answer the TESS questionnaire at their follow-up visit after surgery. The time needed for the completion of the questionnaire was recorded for each participant. To examine the test–retest reliability, patients were asked to complete the same TESS questionnaire 1 week later. All the patients returned the second questionnaire used for analysis. The data were collected by an author (S.W.) who was kept blind of the patients’ diagnosis or treatment.
To examine the convergent validity, the patients were also asked to complete the Musculoskeletal Tumor Society (MSTS) Rating Scale, and the Quality of Life Questionnaire Core 30 of European Organization for Research and Treatment of Cancer (EORTC QLQ-C30). The MSTS Rating Scale is a widely used functional score for patients with extremity sarcoma (Rebolledo et al. 2013). It consists of factors pertinent to the patient, including pain, function, emotional acceptance, use of any external support, walking ability, and gait alteration. A value of 0–5 points (maximum overall score, 30 points) was assigned to each of these factors. The QLQ-C30 is a 30-item questionnaire used to evaluate the function and QoL in cancer patients (Fitzsimmons et al. 1999). The following scales among the functional scales of QLQ-C30 were used in this study, including physical functioning (PF), role functioning (RF), social functioning (SF) and QoL. A high score on the functional scales represents a high level of QoL and a high level of functionality.
Confirmatory factor analysis was carried out with each factor being specified to load on its subscale. Model fit was assessed with the following parameters, including the comparative fit index (CFI), the normed fit index (NFI), root-mean square error of approximation (RMSEA), and the 90 % confidence intervals (CIs) of RMSEA. A good fit of the model was indicated by ratios between the Chi square test and degrees of freedom less than 3, CFI and NFI values not less than 0.90, and RMSEA not more than 0.08.
SPSS for Windows version 16.0 statistical software (SPSS, Chicago, IL, USA) was used for statistical analyses. Descriptive demographic data and scores were reported as mean values ± standard deviation. The test–retest reliability was examined using intra-class correlation coefficient (ICC). The internal consistency was evaluated by Cronbach’s α, with a value >0.70 considered acceptable. To determine the convergent validity of the TESS, correlations between similar domains of the TESS and the QLQ-C30 or the MSTS were analyzed by Pearson correlation analysis. The correlation coefficient larger than 0.40 was considered to indicate adequate convergent validity.
Baseline characteristics of the patients
Patients (n = 64)
47.5 ± 15.2
Time from surgery (year)
1.9 ± 1.2
Undifferentiated pleomorphic sarcoma
Reliability test of the simplified Chinese version of the TESS
ICC (95 % CI)a
Patients’ score of the TESS, the MSTS and the QLQ-C30
(n = 41)
(n = 23)
83.4 ± 19.5
92.3 ± 22.7
25.5 ± 6.5
23.1 ± 4.3
77.4 ± 25.3
78.9 ± 18.4
66.3 ± 23.2
68.2 ± 21.5
72.1 ± 15.6
70.8 ± 20.3
Quality of life
69.3 ± 24.1
66.4 ± 26.2
Convergent validity of the Chinese TESS
Lower extremity (r)
Upper extremity (r)
Quality of life
Factor analysis of the Chinese TESS
90 % CI
The original TESS questionnaire was a valid, reliable and sensitive self-reported instrument to evaluate the functional outcome of sarcoma patients. To date, different language versions of the TESS have been validated in Western and Asian populations (Davis et al. 1996; Saraiva et al. 2008; Saebye et al. 2014; Kim et al. 2015; Ogura et al. 2015). For the first time, this study sought to validate the cross-culturally adapted Chinese version of the TESS. During our translation of the TESS into Chinese, cross-cultural bias was taken into account according to the guidelines reported by Guillemin et al. (Guillemin et al. 1993). A few cultural discrepancies were encountered and some items of the TESS were therefore modified accordingly. The question on sexual activity was omitted from the questionnaire due to the high incidence of “not applicable”. Comparably, there was also a high rate of “not applicable” regarding the question on sexual activity in the Korean and Japanese version of the TESS (Kim et al. 2015; Ogura et al. 2015). We believed that it might be attributed to the different cultural background between the Asian and Western populations. Besides, “cutting food while eating” was replaced by “using chopsticks when eating” as the majority of the Chinese use chopsticks at meals instead of a knife and fork. After translation and cross-cultural adaptation, the mean completion time of the TESS was short and comparable with results reported by other studies. Therefore, we confirmed that the Chinese version of the TESS could be clearly understood and easily administered to the patients.
Compared with other language versions of the TESS, the Chinese TESS showed similar test–retest reliability, internal consistency and validity. The ICCs of 0.93 for the upper extremity questionnaire and 0.89 for the lower extremity questionnaire demonstrated a high level of reliability. Comparably, Saebye et al. (2014) reported the ICC for the upper and lower extremity questionnaires in the Danish population were 0.96 and 0.88 (95 % CI 0.697–0.956), respectively. In a recent study performed in the Korean population, Kim et al. (2015) reported ICCs of 0.979 for the upper extremity TESS and 0.874 for the lower extremity TESS respectively. In our study, Cronbach’s α value for internal consistency was 0.953 and 0.921 for the lower and the upper extremity questionnaire, respectively. Similarly, the internal consistency of the lower and the upper extremity questionnaire reported in previously studies was 0.90 and 0.94 in Denmark and 0.978 and 0.989 in Korea (Saebye et al. 2014; Kim et al. 2015). To investigate the convergent validity, comparisons were made among the TESS, the MSTS and the functional part of the QLQ-C30. We chose the MSTS and QLQ-C30 as they are reliable questionnaires developed for cancer patients. Our results showed that there were good correlations between the TESS and the MSTS and between the TESS and the QLQ-C30. The Pearson correlation coefficients indicated significantly moderate to high correlations between the TESS and the other two questionnaires. Collectively, we believed that the current Chinese version of the TESS questionnaire could well maintain the properties of the original version to measure the QoL of sarcoma patients.
The TESS validation study reported here reflects the rising importance of expanding our knowledge on the physical function of extremity sarcoma patients. As indicated by the good correlation with the PF scale of QLQ-C30, the TESS can specifically evaluate variable levels of physical function. However, other important domains of QoL, including body image, mental status and social activities were not taken into account when applying the TESS to patients with musculoskeletal tumors. Design of such a disease-specific instrument that can evaluate HRQOL for patients with musculoskeletal tumors comprehensively is awaited.
Several limitations still exist in the current study. First, the present study did not test the ability of the TESS to detect the responsiveness of patients to the treatment, which was limited mainly by a relatively small number of patients. A larger sample size is therefore recommended for to clarify this result in future studies. Second, we did not investigate the relationship between the TESS scores and time from surgery or type of surgery. Herein, further investigation into the sensitivity of the TESS to detect the HRQOL in patients with different time from surgery or undergoing different types of surgery was warranted.
In conclusion, we have translated the TESS questionnaire into Chinese and validated the questionnaire. Our results showed that Chinese version of the TESS is a comprehensible, reliable, and valid instrument and can be utilized for future cross-cultural international studies of extremity sarcoma.
LX collected the data and drafted the manuscript. MS and WS performed the statistical analysis. ZZ conceived of the study and participated in its design. QX and SW helped to draft the manuscript. All authors read and approved the final manuscript.
This work was supported by the National Natural Science Foundation of China (Grant No. 81501849 & No. 81201385) and by the Nanjing Key Program of Medical Science and Technology Development (Grant No. ZKX14021).
The authors declare that they have no competing interests
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors.
Informed consent was obtained from all individual participants included in the study.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
- Bekkering WP, Vlieland TP, Koopman HM et al (2009) The Bt-DUX: development of a subjective measure of health-related quality of life in patients who underwent surgery for lower extremity malignant bone tumor. Pediatr Blood Cancer 53:348–355View ArticleGoogle Scholar
- Borden EC, Baker LH, Bell RS et al (2003) Soft tissue sarcomas of adults: state of the translational science. Clin Cancer Res 9:1941–1956Google Scholar
- Davis AM, Wright JG, Williams JI et al (1996) Development of a measure of physical function for patients with bone and soft tissue sarcoma. Qual Life Res 5:508–516View ArticleGoogle Scholar
- Enneking WF, Dunham W, Gebhardt MC et al (1993) A system for the functional evaluation of reconstructive procedures after surgical treatment of tumors of the musculoskeletal system. Clin Orthop Relat Res 286:241–246Google Scholar
- Fitzsimmons D, Johnson CD, George S et al (1999) Development of a disease specific quality of life (QoL) questionnaire module to supplement the EORTC core cancer QoL questionnaire, the QLQ-C30 in patients with pancreatic cancer. EORTC Study Group on Quality of Life. Eur J Cancer 35:939–941View ArticleGoogle Scholar
- Griesser MJ, Gillette B, Crist M et al (2012) Internal and external hemipelvectomy or flail hip in patients with sarcomas: quality-of-life and functional outcomes. Am J Phys Med Rehabil 91:24–32View ArticleGoogle Scholar
- Guillemin F, Bombardier C, Beaton D (1993) Cross-cultural adaptation of health-related quality of life measures: literature review and proposed guidelines. J Clin Epidemiol 46:1417–1432View ArticleGoogle Scholar
- Hoffmann C, Gosheger G, Gebert C et al (2006) Functional results and quality of life after treatment of pelvic sarcomas involving the acetabulum. J Bone Joint Surg Am 88:575–582View ArticleGoogle Scholar
- Kim HS, Yun J, Kang S et al (2015) Cross-cultural adaptation and validation of the Korean Toronto Extremity Salvage Score for extremity sarcoma. J Surg Oncol 112:93–97View ArticleGoogle Scholar
- Lopez-Guerra JL, Marquez-Vega C, Praena-Fernandez JM et al (2011) Health related quality of life and late side effects of long-term survivors of Ewing’s sarcoma of bone. J BU ON 16:528–536Google Scholar
- Ogura K, Uehara K, Akiyama T et al (2015) Cross-cultural adaptation and validation of the Japanese version of the Toronto Extremity Salvage Score (TESS) for patients with malignant musculoskeletal tumors in the lower extremities. J Orthop Sci 20:1098–1105View ArticleGoogle Scholar
- Rebolledo DC, Vissoci JR, Pietrobon R et al (2013) Validation of the Brazilian version of the musculoskeletal tumor society rating scale for lower extremity bone sarcoma. Clin Orthop Relat Res 471:4020–4026View ArticleGoogle Scholar
- Ruggieri P, Mavrogenis AF, Mercuri M (2011) Quality of life following limb-salvage surgery for bone sarcomas. Expert Rev Pharmacoecon Outcomes Res 11:59–73View ArticleGoogle Scholar
- Saebye C, Safwat A, Kaa AK et al (2014) Validation of a Danish version of the Toronto Extremity Salvage Score questionnaire for patients with sarcoma in the extremities. Dan Med J 61:A4734Google Scholar
- Saraiva D, de Camargo B, Davis AM (2008) Cultural adaptation, translation and validation of a functional outcome questionnaire (TESS) to Portuguese with application to patients with lower extremity osteosarcoma. Pediatr Blood Cancer 50:1039–1042View ArticleGoogle Scholar
- Schreiber D, Bell RS, Wunder JS et al (2006) Evaluating function and health related quality of life in patients treated for extremity soft tissue sarcoma. Qual Life Res 15:1439–1446View ArticleGoogle Scholar