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Ann Thorac Surg 2002;73:1541-1544
© 2002 The Society of Thoracic Surgeons
a General Thoracic Surgical Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA
b Medical Oncology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA
c Radiation Oncology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA
Accepted for publication January 23, 2002.
* Address reprint requests to Dr Wright, Blake 1570, Massachusetts General Hospital, Boston, MA 02114 USA
e-mail: wright.cameron{at}mgh.harvard.edu
| Abstract |
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Methods. This was a single-institution, retrospective study.
Results. From 1985 to 2000, 35 consecutive patients underwent induction treatment followed by resection of a superior sulcus tumor. All patients had mediastinoscopy first to exclude N2 disease, and all were N0 at final pathologic examination. Twenty patients had induction RT (mean, 39 Gy), and 15 had induction CT/RT (mean, 51 Gy) with concurrent cisplatin-based chemotherapy. There was no treatment mortality. Complete resection was performed in 16 of 20 (80%) of the RT patients and in 14 of 15 (93%) of the CT/RT patients (p = 0.15). The pathologic response from the induction treatment was complete or near complete in 7 of 20 (35%) of the RT patients and in 13 of 15 (87%) of the CT/RT patients (p = 0.001). The median follow-up was 167 months in the RT patients and 51 months in the CT/RT patients. Two-year and 4-year survival was 49% and 49% (95% confidence interval, 26% to 71%) in the RT patients and 93% and 84% (95% confidence interval, 63% to 100%) in the CT/RT patients, respectively (p = 0.01). The local recurrence rate was 6 of 20 (30%) in the RT patients and 0 in the CT/RT patients (p = 0.02).
Conclusions. Induction CT/RT for superior sulcus tumors appears to offer improved survival compared with induction RT alone.
| Introduction |
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| Patients and methods |
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Patient evaluation
All patients had a chest computed tomographic scan, which included the liver and adrenal glands, and a diagnosis made by fine-needle aspiration. All had routine brain and bone scans to exclude occult metastatic disease. Since 1990, the majority of patients (70%) have had a magnetic resonance scan of the thoracic inlet area to delineate the anatomy. All patients had mediastinoscopy before starting induction treatment, and all were found to be negative for N2 nodal metastases.
Radiation therapy
The radiation target included the primary tumor, ipsilateral hilum, mid and upper mediastinum, and ipsilateral supraclavicular regions. Patients having induction RT had a preoperative mean dose of 39 Gy (range, 27 to 64 Gy) delivered in 2-Gy fractions, and the majority of patients had a postoperative boost dose (mean, 10 Gy; range, 0 to 27 Gy). Patients who had induction CT/RT had a preoperative mean dose of 51 Gy (range, 40 to 66 Gy). Four patients had hyperfractionated RT with 180 cGy given twice daily [8]. One CT/RT patient with an incomplete resection had postoperative RT.
Chemotherapy
Four patients had two preoperative and one postoperative cycles of concurrent chemotherapy consisting of cisplatin 100 mg/m2 on day 1, 5-fluoruracil 30 mg/kg per day for 3 days starting day 1, and vinblastine 4 mg/m2 on day 1 [8]. Eleven patients had two preoperative cycles of concurrent chemotherapy consisting of cisplatin 50 mg/m2 on days 1, 8, 29, and 36 and etoposide 50 mg/m2 on days 1 to 5 and 29 to 33 [9]. Five patients had two additional cycles of the same chemotherapy postoperatively based on residual tumor in the resection specimen.
Statistical analysis
Survival was estimated by the product-limit method of Kaplan and Meier, and curves were compared by the log-rank test. Cox regression analysis was used to assess prognostic factors for their significance in predicting survival. Categorical variables were compared by the
2 test. Continuous variables were compared with the Students t test. All significance values were two-tailed.
| Results |
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There was no difference in distant recurrences between the two induction groups (Table 3). There was a reduction in local recurrence in the CT/RT induction patients (p = 0.02).
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| Comment |
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Induction CT/RT was remarkably effective at sterilizing the tumor, with a 67% complete response rate and an 87% rate of near or complete response. It is likely that the improved survival seen was caused in large part by this very high sterilization rate.
Two previously published reports have also suggested that CT/RT is the optimal induction strategy for superior sulcus tumor patients. Martinez-Monge and coworkers [11] in 1994 reported 18 patients treated with two different mitomycin, vindesine, and cisplatin regimens. There was a very high treatment mortality rate of 17%, a high pathologic complete response rate (71%), and a favorable 56% 4-year survival rate. Attar and associates [12] in 1998 briefly reported on 11 patients treated with carboplatin and paclitaxel. Treatment toxicity was not stated, but the 5-year survival was 72%. Rusch and colleagues [13] recently reported a large prospective multiinstitutional trial (Intergroup 0160) of induction CT/RT (based on Southwest Oncology Group 8805 [9]) for superior sulcus tumors. There were 111 eligible patients, and 102 had the planned induction treatment. There were 5 (5%) treatment-related deaths. Eighty-three patients underwent thoracotomy, and 76 (92%) had a complete resection. The pathologic response to induction CT/RT was complete or with only minimal microscopic residual disease in 65% of the patients. The 2-year and 4-year survival was 55%. The complete resection rate was high (90%), and the locoregional recurrence rate was low (23%). The authors concluded that the complete resection rate and survival appeared improved compared with historic experience. A randomized trial of therapy in this small subset of patients with nonsmall-cell lung cancer will probably never be accomplished because of the rarity of this tumor. Accordingly, careful scrutiny of the Intergroup trial and the other case series with comparison to historic experience with induction RT is necessary to determine whether an apparent improvement in care is real. Our series is particularly helpful in this regard inasmuch as there is a period of time during which the two induction programs overlapped, the patients were carefully staged both radiographically and by mediastinoscopy, and the surgical strategy was uniform. A fair comparison between the two induction programs might conclude that induction CT/RT (1) can be given with acceptably low morbidity, (2) trends toward a higher complete resection rate, (3) results in a very high pathologic response rate, (4) results in a reduced locoregional recurrence rate (the ultimate test of the completeness of resection), and (5) offers improved survival.
There are several limitations of our study. The first is the retrospective nature of this consecutive case series in which treatment was not by protocol. The second is that there may have been case selection bias favoring better patients undergoing induction CT/RT. However, the three major prognostic factors were fairly evenly distributed between the two groups, and there were more T4 tumors in the CT/RT group. Third, there was probably also an element of time selection bias favoring the CT/RT patients who likely benefited from better staging (new spiral computed tomographic scan), improved surgical procedure owing to use of the anterior approach and the learning effect, and a general improvement of care that comes with the time. Nonetheless, many patients were treated simultaneously with both induction programs, and all patients were vigorously staged. Fourth, the median follow-up was longer in the RT patients, which allows more time for failure. Lastly, the sample size is small, and several comparisons (complete resection rate and length of stay) would likely have been significant if the study were larger (type II error).
Induction CT/RT followed by resection for superior sulcus tumors appears superior to the historic approach of induction RT alone. Future trials should investigate the feasibility of dose escalation of radiation as medium-dose RT (50 Gy) appears well tolerated and local control is still not ideal [14]. Other chemotherapeutic agents that act as radiation sensitizers should be evaluated in these patients now that a baseline pathologic response rate has been established for the standard regimen of cisplatin and etoposide. Adjuvant postoperative chemotherapy and central nervous system prophylaxis need to be investigated as distant metastases now represent the most common site of failure.
| References |
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