15018752330
发表时间:2015-12-08 浏览次数:455次
Introduction
Soft tissue sarcomas (STSs) are a rare group of heterogeneous malignant tumors derived from mesenchymal cell lines. [1] They represent approximately 1% of all malignancies. [2],[3],[4]
STS can occur at any age, but the peak of incidence is in the late
adult life. Introduction of multidisciplinary teams and referral of
patients to specialized care units with diagnostic radiology,
histopathology, surgical expertise and neoadjuvant and adjuvant therapy
has improved the management of STS. [1]
The Hospital District of North Savo is comprised of 7 hospital areas
and 855,000 (year 2000) and 843,000 (year 2009) inhabitants. The
multidisciplinary STS group of Kuopio University Hospital was
established in 1994. The group meets on a weekly basis to discuss the
best approach for each patient with STS utilizing a multidisciplinary
team.
In this study, we analyzed all patients whose sarcoma was
evaluated by this multidisciplinary team over a 10 years period:
2000-2009. At the beginning of the study, the algorithm for examination
and treatment in primary health care for STS was not what it is today.
To increase awareness regarding tumor diagnostics, accurate biopsy
methodology and imagining, the current clinical practice guidelines were
introduced to the primary care units and tertiary centers by lectures
and bulletins. Guidelines included tumor characteristics necessitating
referral to specialized units. These were a fast-growing mass, diameter
wider than 5 cm, location close to the deep fascia, development of pain
in a previously painless lump and a newly formed tumor in the same
location as benign tumor noted previously.
In order to measure
the impact of the multidisciplinary groups and clinical guidelines, we
divided the time period into 2 parts and compared the results of
treatment. The first period, Group A, comprised the early part of the
study (2000-2005) when the knowledge was still poor. The last 4 years
after introduction of guidelines (2006-2009) comprised the second period
as Group B.
The aim of this study was to determine, if there
were any differences in the outcome of STS in Hospital District of North
Savo, when diagnostic methods, the treatment results, local
recurrences, metastases, and overall survival were analyzed between the 2
periods.
Methods
All the material was retrospectively collected from the files of multidisciplinary sarcoma group meetings. Accordingly the patients' medical reports were reviewed for medical data. The patient demographics were collected [Table 1]. The interval between the symptoms and the histological sample collection was measured, and information about tumor characteristics (the type of the sarcoma, tumor size, location, grade, sample collection method, metastasis, and recurrence) were clarified [Table 1]. In addition, we studied if there were any previous condition, which required surgical intervention in the sarcoma site. Furthermore, the patients' previous oncological treatments before the sarcoma diagnosis were examined [Table 1]. Desmoid tumors were excluded from the study.
Samples were studied by an experienced pathologist, (Professor Ylermi
Soini), and classified according to the guidelines of the World Health
Organization: classification of soft tissue and bone tumors using
routine H and E staining and immunohistochemistry including vimentin,
desmin, S-100, protein CD34, sytokeratin PAN (AE1/AE3), Ki67 (all from
Roche Biotechnology) and desmin (Dako, Glostrup, Denmark) and stained
with an automatic immunostainer (Ventana and Dako).
Statistical analyses were done with Statistical Package for the Social Sciences SPSS® Base version 18 (SPSS, Inc., Chicago, Illinois, USA).
The
study was approved by the Ethical Committee of Kuopio University
Hospital, and all patients gave their written informed consent for
participation in the study 15/2009.
Results
One hundred and thirty-five patients with STS were treated in Kuopio University Hospital between 2000 and 2009 [Table 1].
Seventy-four (55%) of them were men and 61 (45%) women. Average age for
the all patients was 59 years (64 mean (13-89)). Only 2 of the patients
were under 18 years. The mean follow-up time was 68 months (range:
12-149).
Annual incidence of STS in Group A was 1.39/100, 000 (inhabitants) and 1.89/100,000 in Group B.
Soft tissue sarcoma histology
When
the total time period (2000-2009) was analyzed, the most common
sarcomas in descending order were found to be pleomorphic sarcoma (37%),
liposarcoma (26%), fibrosarcoma (10.4%) and leiomyosarcoma (9.6%) [Table 2].
Pleomorphic sarcoma was equally common in both genders (38%), as so was
leiomyosarcoma (men 9.5%, women 9.8%). Fibrosarcoma was found to be
more than twice as common in men (14.9%) than women (6.6%).
Liposarcomas, fibrosarcomas, synovial sarcomas and chondrosarcomas
occurred usually in young adults and in middle-aged people. Among
elderly patients' liposarcomas and pleomorphic sarcomas were the most
common tumors. The incidence of leiomyosarcomas was same in all age
groups studied.
Tumor location
In this study, 78 patients (58%) had a tumor in their lower limb and 20 tumors were diagnosed below the knee [Table 2].
Thirty-one patients (23%) had a tumor in the trunk, 22 (16%) in the
upper limb and 3 (2%) in the head or neck region. In Group A, 46
patients (65%) had sarcoma in the lower limb, 14 (20%) in the trunk, 10
(14%) in the upper limb and 1 (1%) in the head and neck region.
In
the latter Group B, 32 patients (50%) had sarcoma in the lower limb, 17
(27%) in the trunk, 12 (19%) in the upper limb and 2 (3%) in the head
and neck.
Sampling method
In this study, 89 tumors
(66%) were diagnosed with core needle biopsy (CNB), 5 (4%) with a
fine-needle biopsy, while 24 tumors (18%) were excised for the histology
and 14 (10%) were analyzed by incisional biopsy (excision with positive
margins). In Group A, 47 were (66%) diagnosed with CNB, 11 (16%) with
excisional resection, 2 (3%) with fine-needle aspiration biopsy (FNAB)
and 9 (13%) with incisional biopsy. In the Group, B 42 were (66%)
diagnosed with CNB, 13 (20%) with excisional resection, 3 (5%) with FNAB
and 5 (8%) with incisional resection. The number of tumors that were
diagnosed by incisional biopsy was found to be high if the tumor was
located in the upper limb (P = 0.002). These incisional biopsies
were performed in tertiary centers or in local hospitals without
consulting specialists. However, there were no statistical difference
between the sampling methods used when occurrence of metastases, local
recurrence or death were analyzed.
Treatment
The
most common surgical treatment was wide local excision (56 patients,
42%). Total myectomy was done for 49 patients (36%) and amputation for
13 patients (10%). Seventeen patients (13%) were treated conservatively.
When comparing the groups, there were no differences between operation
methods except for the amputation rate. Limb amputation were done to 11
patients in Group A, whereas only 2 in Group B. In this study, 63
patients (47%) received radiotherapy and 15 patient's chemotherapy
(11%). There were no differences in adjuvant therapy between the 2
groups.
Survival
In Group A, 10 patients (14%) got a recurrence tumor during the follow-up period and in Group B 12 patients (19%) [Table 3].
All the recurrences occurred within 2.5 years (range: 1-27 months)
after the primary operation. Twenty-two of all patients (16%) got a
recurrence during 2 years' follow-up.
In Group A, 8 out of 10 recurrences were high-grade tumors (7
pleomorphic sarcoma, 1 leiomyosarcoma). Two tumors were low-grade
sarcomas (liposarcomas). Six of the 10 patients died with recurrences
during the follow-up time of 5 years.
In Group B, 12 tumors
recurred, from which 5 were pleomorphic sarcomas, 3 liposarcomas, 2
fibrosarcomas, and 2 angiosarcomas. Ten of these 12 tumors were
high-grade tumors. One was a low-grade liposarcoma, which was diagnosed
by incisional biopsy. Four patients were diagnosed with an excisional
biopsy, and 3 were operated intralesionally for diagnosis. Four patients
got lung metastases and 8 died during the follow-up time. There were no
significant differences in local recurrence between the 2 groups.
A total of 22 patients (16%) had metastases, of which the most common sites were lung, bone and lymph nodes [Table 3].
Two skin metastases were found in patients with pleomorphic sarcoma, 5
patients had lymph nodes metastases (chondrosarcoma, liposarcoma,
pleomorphic sarcoma and fibrosarcoma), and 4 patients had bone
metastases (pleomorphic sarcoma, liposarcoma and malignant schwannoma).
During
the follow-up time, 7 patients (10%) in Group A got metastases, whereas
in the Group B incidence of metastases was higher (15 patients, 23%) (P = 0.033).
A
total of 48 patients (36%) died during the follow-up time. Seventeen
patients were treated conservatively without surgical intervention.
These patients were either unsuitable for operation because of their
co-morbidity, or they declined the surgery. Among all the patients who
underwent surgery, mortality rate was 23% (31 patients).
In Group
A, 21 patients (30%) died during the follow-up period whereas 27
patients (42%) died in the Group B. All deaths occurred within 22 months
after the diagnosis (range: 1 month-6 years with a median period of
12.5 months). There were no statistical significance differences in
overall survival between the groups for the follow-up period but there
was a difference in the survival for the 1st year [Figure 1]. The 1st year survival was 100% in the Group A and 87% in the Group B.
Discussion
The present study shows that increasing the general awareness about STS
management among general practitioners did not improve either the
results or the survival. But it may have improved the referral rate
after the knowledge about tumor diagnostics improved. In the latter
years of the study, the number of sarcoma patients increased. In the
year 2001 there were 8 patients diagnosed with STS, in 2008; 19 patients
and in 2009; 15 patients. This likely resulted from improved knowledge
of these tumors by primary care practitioners and improved referral
patterns to specialized units.
When comparing our single
institution's STS results with a nationwide population based study in
Finland, no statistically significant differences in surgical treatment,
local recurrence, metastasis or survival were noted. [5] STS local recurrence in our series was 22% and as opposed to 30% in earlier studies. [1]
In this study, Group B had more metastases [Figure 1]
a lower survival rate as well as a shorter survival time. We also noted
that the 1st year survival was better in Group A. Because this was a
retrospective study, we were not able to analyze the effect histologic
grading on cervical. Between the years, 2000 and 2009 sarcomas were
primarily divided into 3 histologic grades: grade I presenting the
low-grade tumors and Grade II and III the high-grade tumors. This
histological grading system is proposed by the French Federation of
Cancer Centers and is the most commonly used system for assigning tumor
grading. [6],[7]
Although there were only minimal differences in grading between the
groups, it is notable that Grade III tumors were equally prevalent in
the 2 groups studied: (A: 43%, B: 45%).
Despite the grading, we
found that tumors in the Group B to be more likely to have metastases
with a lower overall survival rate. After consideration of all
parameters studied, we found that there were more trunk sarcomas in the
Group B. Many studies have shown that sarcomas located in the trunk
(chest wall, internal trunk and retroperitoneum) have a worse prognosis
and a higher rate for local recurrence. [1],[8],[9]
This is mainly due to the difficulty of gaining adequate resection
margins and lack of thick barriers such as the muscle fascia's.
Interestingly,
a remarkable number of upper limb tumors were diagnosed by an
incisional biopsy. This was done in either tertiary centers or local
hospitals with appropriate consulting. Presumably, the delay between
detecting the lump and getting treatment was short because upper limb
tumors are easily found by the patients themselves, and even small
tumors are visible in this area. However, this study showed that even
though the tumors were biopsied incisionally, this did not result in
cancer spreading or poor survival. The patients whose tumors were
incisionally biopsied had the same outcomes with those whose tumors were
diagnosed according to the national practice guidelines. According to
the literature, the risk of residual tumor tissue is 24-60% after an
unplanned surgery [10],[11] and therefore confirms the fact that unplanned surgery increases the risk of local recurrence. [12],[13] But still many patients are operated in tertiary centers without accurate imagining and biopsy. [14],[15]
There were many patients who had had a previous benign tumor in the
same location. In addition to the previous tumor diagnosis and
treatment, the newly formed tumor should always be examined as an
independent disease, according to the recommendations. Furthermore, we
found that in some cases histological evaluation was never made and thus
the diagnosis was delayed.
National guidelines are still not
being followed correctly. Sarcomas are being incisionally biopsied
without appropriate imagining. A failure to implement guidelines is
primarily due to the rarity of this malignancy. Only a few doctors come
to face STS during their practice and therefore the guidelines are not
easy to remember. To increase the awareness of tumor diagnostics, the
national guidelines should be effectively and repeatedly processed in
tertiary centers. Written recommendations in the Internet are not
enough. Guidelines have to be introduced by personal education,
lectures, and program with easy availability to all doctors who take
part in referring patients to specialized units.
References
1.Cutts S, Andrea F, Piana R, Haywood R. The management of soft tissue sarcomas. Surgeon 2012;10:25-32.
2.Gronchi A, Lo Vullo S, Colombo C, Collini P, Stacchiotti S, Mariani L, Fiore M, Casali PG. Extremity soft tissue sarcoma in a series of patients treated at a single institution: local control directly impacts survival. Ann Surg 2010;251:506-11.
3.King DM, Hackbarth DA, Kirkpatrick A. Extremity soft tissue sarcoma resections: how wide do you need to be? Clin Orthop Relat Res 2012;470:692-9.
4.Khatri VP, Goodnight JE Jr. Extremity soft tissue sarcoma: controversial management issues. Surg Oncol 2005;14:1-9.
5.Popov P, Tukiainen E, Asko-Seljavaara S, Huuhtanen R, Virolainen M, Virkkunen P, Blomqvist C. Soft-tissue sarcomas of the upper extremity: surgical treatment and outcome. Plast Reconstr Surg 2004;113:222-30.
6.Nystrom LM, Reimer NB, Reith JD, Dang L, Zlotecki RA, Scarborough MT, Gibbs CP Jr. Multidisciplinary management of soft tissue sarcoma. Scientific World Journal 2013;2013:852462.
7.Trojani M, Contesso G, Coindre JM, Rouesse J, Bui NB, de Mascarel A, Goussot JF, David M, Bonichon F, Lagarde C. Soft-tissue sarcomas of adults; study of pathological prognostic variables and definition of a histopathological grading system. Int J Cancer 1984;33:37-42.
8.Gutierrez JC, Perez EA, Franceschi D, Moffat FL Jr, Livingstone AS, Koniaris LG. Outcomes for soft-tissue sarcoma in 8249 cases from a large state cancer registry. J Surg Res 2007;141:105-14.
9.Sugiura H, Nishida Y, Nakashima H, Yamada Y, Tsukushi S, Yamada K. Surgical procedures and prognostic factors for local recurrence of soft tissue sarcomas. J Orthop Sci 2014;19:141-9.
10.Venkatesan M, Richards CJ, McCulloch TA, Perks AG, Raurell A, Ashford RU; East Midlands Sarcoma Service. Inadvertent surgical resection of soft tissue sarcomas. Eur J Surg Oncol 2012;38:346-51.
11.Chandrasekar CR, Wafa H, Grimer RJ, Carter SR, Tillman RM, Abudu A. The effect of an unplanned excision of a soft-tissue sarcoma on prognosis. J Bone Joint Surg Br 2008;90:203-8.
12.Rutkowski P, Trepka S, Ptaszynski K, Kolodziejczyk M. Surgery quality and tumor status impact on survival and local control of resectable liposarcomas of extremities or the trunk wall. Clin Orthop Relat Res 2013;471:860-70.
13.Alamanda VK, Crosby SN, Archer KR, Song Y, Schwartz HS, Holt GE. Predictors and clinical significance of local recurrence in extremity soft tissue sarcoma. Acta Oncol 2013;52:793-802.
14.Nijhuis PH, Schaapveld M, Otter R, Hoekstra HJ. Soft tissue sarcoma - compliance with guidelines. Cancer 2001;91:2186-95.
15.Qureshi YA, Huddy JR, Miller JD, Strauss DC, Thomas JM, Hayes AJ. Unplanned excision of soft tissue sarcoma results in increased rates of local recurrence despite full further oncological treatment. Ann Surg Oncol 2012;19:871-7.