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J Thorac Cardiovasc Surg 2008;135:642-647
© 2008 The American Association for Thoracic Surgery
General Thoracic Surgery |
a Department of Surgery, Mount Sinai Medical Center, New York, NY
b Department of Medicine, Mount Sinai Medical Center, New York, NY
c Department of Pathology, Mount Sinai Medical Center, New York, NY
d Division of Thoracic Surgery, Mount Sinai Medical Center, New York, NY
Received for publication March 7, 2007; revisions received September 10, 2007; accepted for publication September 24, 2007. * Address for reprints: Scott Swanson, MD, Mount Sinai Medical Center, 1190 Fifth Avenue, New York, NY 10029. (Email: scott.swanson{at}mountsinai.org).
| Abstract |
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Methods: We collected data from 153 consecutive patients who underwent thorascopic (video-assisted thoracic surgery) lobectomy and assessed the perioperative outcomes, postoperative pain, and chemotherapy course. A total of 111 of 127 patients with lung cancer had stage I non–small cell lung cancer. The operative technique required 2 ports and an access incision (5–8 cm), individual hilar ligation, and lymph node dissection performed without rib-spreading devices.
Results: There were 9 major complications (6%), including 1 perioperative death (0.7%). Conversion to thoracotomy occurred in 14 patients (9.2%). Blood transfusion was required in 11 patients (7%). The median chest tube time was 3 days, and the length of hospital stay was 4 days; 94.4% of patients went home at the time of discharge, and 5.6% of patients required a rehabilitation facility. At a median postsurgical follow-up time of 2 weeks, the mean postoperative pain score was 0.6 (0–3), 73% of patients did not use narcotics for pain control, and 47% of patients did not use any pain medication. Of patients receiving chemotherapy (N = 26), 73% completed a full course on schedule and 85% received all intended cycles.
Conclusion: Thoracoscopic (video-assisted thoracic surgery) lobectomy can be performed safely. Discharge independence and low pain estimates in the early postoperative period suggest that this approach may be beneficial. Furthermore, there is a trend toward improved tolerance of chemotherapy.
| Introduction |
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Thoracoscopic (video-assisted thoracic surgery [VATS]) lobectomy has been used in the treatment of lung cancer since the early 1990s and has become an accepted method of lobectomy.1
Several small VATS series reported that VATS lobectomy is technically feasible and safe. In our series, the data confirm results obtained in other retrospective series with regard to low mortality and morbidity. We provide additional data about postoperative pain control, discharge disposition, and tolerance of chemotherapy.
| Materials and Methods |
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Patients were included in the VATS cohort study data if the preoperative surgical goal was thoracoscopic lobectomy regardless of whether the surgery was completed thoracoscopically. However, if our intention was to perform an exploratory thoracoscopy to rule out pleural disease, and a subsequent resection by thoracotomy was performed, the case was excluded from the VATS series.
All patients with stages I and II lung cancer who did not have contraindications to the procedure were eligible for VATS lobectomy. The VATS study exclusion criteria were the standard absolute contraindications to VATS lobectomy and included the presence of T3 or T4 tumors, N3 disease, or inability to achieve single-lung ventilation. Relative contraindications included central hilar tumors, tumors that were visible on bronchoscopy or necessitated sleeve resection, bulky mediastinal or hilar lymphadenopathy, and a history of neoadjuvant chemotherapy or radiation.
If a conversion was necessary, patients remained in this cohort on the basis of the principle of "intention to treat." All cases were discussed with the operating surgeon. Operative notes were reviewed, and the goals for the surgical procedures were discussed. Thus, we were able to distinguish patients who underwent thoracoscopy to rule out pleural metastases from those in whom conversions were performed. The operative goal for all patients with presumed non–small cell lung cancer (NSCLC) stages I and II was a thoracoscopic surgical procedure. The reasons for conversions are listed in the "Results" section.
Preoperative studies for VATS lobectomy included chest radiograph, computed tomography scan, bronchoscopy, pulmonary function studies, positron emission tomography scan, and other modalities for metastatic workup when necessary. The type of surgery performed was individualized to the patient and the tumor. Most commonly, we performed lobectomies. However, in patients with poor pulmonary function and smaller tumors, anatomic segmentectomies were performed. A summary of resections performed by anatomic location is shown in
Table 1.
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All patients underwent lymph node dissection. We dissected lymph nodes 2, 4, and 7 to 12 (or hilar) for right-sided tumors, lymph node stations 5 to 12 for left-sided tumors, and 4R, 4L, and 7 for cervical mediastinoscopies. Typically for T1 tumors, we did not perform routine mediastinoscopy unless the preoperative computed tomography scan demonstrated lymphadenopathy greater than 1 cm. We routinely performed mediastinoscopies in patients with positron emission tomography-positive mediastinal adenopathy (standard uptake value > 3) or T2 or greater-sized tumors. After surgery, all patients recovered in the postoperative anesthesia care unit and were transferred subsequently to a monitored care setting.
Chemotherapy
Postoperatively, patients who were eligible received adjuvant chemotherapy according to the Cancer and Leukemia Group B 9633 North American Intergroup JBR.10 (JBR.10) protocols, namely, 4 cycles of paclitaxel and carboplatin for 12 weeks or 4 cycles of cisplatin and vinorelbine for 16 weeks, respectively. Most patients were treated with the Cancer and Leukemia Group B protocol; 1 patient received the JBR.10 protocol.2,3
The adjuvant chemotherapy data were collected from patient charts and interviews, and oncologist interviews. Not all patients received chemotherapy at our institution, but follow-up was complete and all patients were included.
Postoperative Follow-up Care
Data were obtained and analyzed retrospectively. During postsurgical visits, patients were asked by nurse practitioners to grade their level of pain responses in a questionnaire format. Patients evaluated their pain levels on a scale of 0 to 3 (0 = no pain, 1 = mild pain, 2 = moderate pain, 3 = severe pain). In addition, patients categorized their use of medications for pain relief as none, nonsteroidal anti-inflammatory agents, opiates, or both. The postoperative interval of their visit was also recorded. Patients were contacted with approval of the institutional review board for chemotherapy, recurrence, and survival data. Individual consent was waived.
Complications
Major complications were considered mortality, respiratory failure, empyema, atrial fibrillation requiring cardioversion or anticoagulation, and reoperation. Minor complications were considered prolonged air leak, atrial fibrillation not requiring cardioversion and anticoagulation, pneumonia without respiratory failure, deep vein thrombosis, urinary tract infection, and cellulitis from intravenous catheter. These data were collected retrospectively on the basis of chart review, postoperative follow-up visits, discharge summaries, and patient interviews.
Statistical Analysis
Medians and ranges are presented for non-normal data. We used the Kaplan–Meier method to estimate disease-free survivals of patients with stage I NSCLC who underwent VATS lobectomy. To estimate disease-free survival, we treated deaths from causes other than lung cancer as censored observations.
| Results |
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Mortality and Morbidity
There were no intraoperative deaths. There was 1 postoperative death (0.7%) secondary to respiratory failure from aspiration pneumonia. The most common complications were atrial fibrillation in 16 of 153 patients (10.5%) and prolonged air leak more than 7 days in 12 of 153 patients (7.8%). Most patients with atrial fibrillation had a short course, with a majority requiring chemical cardioversion with amiodarone. Two patients underwent electrical cardioversion, and 2 patients were anticoagulated. Some patients experienced more than 1 complication. Other complications are noted in
Table 5.
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Postoperative Pain
At the first postoperative follow-up visit at a median time of 2 weeks (mean 3.1 weeks) postsurgery, patients were asked to assess their level of pain on a scale of 0 to 3 (0 = in no pain; 1 = in mild pain; 2 = in moderate pain; 3 = in severe pain) The mean pain score based on this scale was 0.6 (median 0; range 0–3). Patients (N = 145) also reported the medications they were using for pain relief. At this median follow-up period of 2 weeks, 47% of patients were not using any pain medication, 26% were taking NSAIDs either as needed or standing order, and 27% reported some narcotic use, with most, 22%, taking opiates as needed.
Oncologic Results
Of 127 patients with NSCLC who underwent thoracoscopic lobectomies, 57 (44.9%) had cervical mediastinoscopies, all of which were negative. Seventy patients did not undergo mediastinoscopy. The mean number of lymph node stations sampled from the patients with NSCLC was 4.8 overall (median, 5.0), including mediastinoscopy and lymph node dissection. Eleven patients were diagnosed with positive lymph nodes (11/127; 8.7%) after the thoracoscopic lymph node dissection; 6 of these patients had negative mediastinoscopies.
Chemotherapy
Of the 26 patients who received chemotherapy, 19 (73%) received their full planned dose on schedule and 3 (12%) were administered the full course of planned doses of chemotherapy with a delay in 1 or more cycles. Twenty-two patients (85%) received all intended cycles with or without delay. Reasons for dose delay or dose reduction in our series were neutropenia (n = 2), gastrointestinal symptoms (n = 2), unknown (n = 3), and a combination of symptoms (n = 1).
Survival
Follow-up was complete for all patients with lung cancer. The median follow-up time was 14 months (mean: 16 months; range: 1–40 months). Fourteen patients had recurrences: 1 of 127 patients (0.8%) had a locoregional recurrence at 26 months; 7 of 127 patients (5.5%) had distant recurrences; and 6 of 127 patients (4.7%) had both locoregional and distant recurrences. Our rate of isolated locoregional recurrence is low, but because this is a small group with a short follow-up period, no definite conclusions may be drawn.
Figure 1 summarizes disease-free survival for all patients with NSCLC (follow-up data are for 124 of 127 patients; 3 patients had 2 separate lobectomies for metachronous lesions, and survival data are assessed in each case for only 1 of the 2 surgical procedures).
Figure 2 summarizes all patients with stage I NSCLC.
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| Discussion |
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One criticism of this surgery is the risk of uncontrolled bleeding. Although we recognize that this risk exists, it seems to be minimal and has not been reported in many large series. Should pulmonary arterial injury occur during a VATS procedure, control can easily be achieved with a spongestick, and the surgeon can convert to a thoracotomy. Furthermore, the safety and efficacy of VATS lobectomy have been demonstrated in several small series, some of these prospective and randomized.4-7
The comparative safety profiles between VATS and thoracotomy are similar. Recently, McKenna and colleagues8
published a large series with excellent perioperative outcomes. Perioperative morbidity and mortality with VATS lobectomy compare favorably to those of large series of thoracotomy lobectomies. In the largest series of patients undergoing lobectomy predominantly by thoracotomy, morbidity ranged from 28% to 38% and mortality ranged from 1.2% to 2.9%.9-11
Other VATS lobectomy series have had morbidity rates ranging from 9% to 19%, with perioperative mortality ranging from 0.8% to 1.8%.8,12-15
Oncologic Results
VATS lobectomy is oncologically the same surgical procedure as a lobectomy through a thoracotomy; both use anatomic resection, individual hilar ligation, and lymph node sampling or dissection. Reports indicate that the number of dissected lymph nodes is similar between VATS lobectomy and thoracotomy.16-18
Uniform lymph node counting procedures at this institution were established subsequent to our review so we cannot report the number of lymph nodes dissected per VATS case here. Five-year survivals are comparable and in some cases seemingly better. Walker and colleagues12
reported a 4-year survival of 78% in 117 patients with stage I lung cancer, whereas other studies have reported 5-year survivals as high as 97%.19
This compares with published 5-year survivals between 61% and 82% for patients with stage I surgical lung cancer who undergo thoracotomy, although admittedly a direct comparison would be unfair because VATS data are not based on randomized prospective controlled studies and may be related to patient selection.20,21
Postoperative Pain, Length of Stay, and Discharge Disposition
The greatest advantage of a VATS lobectomy may be an improvement in patients' perioperative quality of life. The pain associated with this surgery is probably less than that experienced by patients who undergo thoracotomy and may in part be explained by decreased inflammation.22
Other series have suggested that this pain is significantly less in the early postoperative period.4,5,7
In a case-control study, Demmy and colleagues23
reported similar discharge data after VATS lobectomies and found that significantly more patients who underwent thoracotomy required skilled nursing facilities after surgery. Thus, the data suggest that these patients have short hospital stays, are discharged without home assistance, and have low opiate requirements.
Chemotherapy
Although we obtained some preliminary data on a small group of patients who underwent both VATS lobectomy and adjuvant chemotherapy, we were not able to make any definitive comparisons with regard to tolerance of chemotherapy compared with open lobectomy groups. There are few data in the literature about how soon after surgery a patient begins adjuvant chemotherapy, although most trials seem to start after a postsurgical interval of 6 weeks. Another recent study reported that patients who underwent VATS had significantly less dose delay and dose reduction, but the interval to delivery of chemotherapy was not significant.24
In comparison, the Cancer and Leukemia Group B trial 9633 reported that 55% of patients received full-dose chemotherapy and the Intergroup JBR.10 trial reported that 45% of patients had at least 1 dose delay.2,3
Approximately 34% of patients in the Adjuvant Lung Project Italy series chemotherapy wing received all scheduled doses without adjustment or delay; 69% completed their treatments with or without adjustments or delay.25
It is conceivable that patients who undergo VATS may have a quicker recovery and in general more strength to tolerate chemotherapy. There are theoretic survival benefits to starting chemotherapy immediately after surgery because the body's tumor burden should be lowest, and tumor growth fastest, at this time. Thus, chemotherapy administered immediately postsurgery would be most effective, assuming that wound healing is adequate.
| Conclusions |
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| Acknowledgments |
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| References |
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