Postoperative adjuvant therapy for stage II non-small-cell lung cancer.

Park, J H; Shim, Y M; Baek, H J; Kim, M S; Choe, D H; Cho, K J; Lee, C T; Zo, J I
The Annals of thoracic surgery
1999Nov ; 68 ( 5 ) :1821-6.
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Park, J H -
Shim, Y M -
Baek, H J -
Kim, M S -
Choe, D H -
Cho, K J -
Lee, C T -
Zo, J I -
ABSTRACT
BACKGROUND: Stage II non-small-cell lung cancer is regarded as one of the early lung cancers. Although resection, including the mediastinal lymph nodes, is currently regarded as the standard treatment, the survival rate of this disease is not encouraging. It is well known that the most common causes of death are locoregional recurrences or distant metastases, or both. However, the best adjuvant treatment to improve survival is as controversial an issue as ever.

METHODS: This study was designed as a randomized, blinded, two-armed study with operation and adjuvant radiotherapy in one arm, versus operation and adjuvant mitomycin C (10 mg/m2), vinblastine (6 mg/m2), and cisplatin (100 mg/m2) (MVP) chemotherapy in the other arm. We assigned 57 resected patients with pathologic proven stage II non-small cell lung cancer to the groups according to our eligibility criteria.

RESULTS: The most common pattern of recurrence was distant metastases, and nearly all the recurrences (17 of 18 patients) in both groups were found within 2 years after operation. The rates of the locoregional and distant metastases were 3.6% and 46.4% in the adjuvant radiotherapy group and 6.9% and 10.3% in the adjuvant chemotherapy group (p = 0.018). The 5-year disease-free survival rates were 52.0% in the adjuvant radiotherapy group and 74.0% in the adjuvant chemotherapy group (p = 0.16, log-rank test). The 2-year, 5-year, and 6-year survival portions were 60.3%, 56.5%, and 28.3% in the adjuvant radiotherapy group, and 82.8%, 70.1%, and 60.1% in the adjuvant chemotherapy group (p = 0.01, p = 0.17, and p = 0.03, Z-test). The difference of the actuarial survival between these two groups was somewhat significant (p = 0.09, log-rank test).

CONCLUSIONS: Our results suggest that the addition of adjuvant MVP chemotherapy may reduce the distant metastasis rates and prolong the survival of the surgically resected stage II non-small-cell lung cancer patients.
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MESH
Adult, Aged, Antineoplastic Combined Chemotherapy Protocols/adverse effects/*therapeutic use, Carcinoma, Non-Small-Cell Lung/drug therapy/pathology/radiotherapy/*surgery, Chemotherapy, Adjuvant, Cisplatin/administration & dosage, Cobalt Radioisotopes/therapeutic use, Combined Modality Therapy, Disease-Free Survival, Female, Follow-Up Studies, Humans, Lung Neoplasms/drug therapy/pathology/radiotherapy/*surgery, Lymph Node Excision, Male, Middle Aged, Mitomycin/administration & dosage, Neoplasm Staging, Pneumonectomy, *Radioisotope Teletherapy, Radiotherapy, Adjuvant, Radiotherapy, High-Energy, Vinblastine/administration & dosage
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The addition of adjuvant MVP chemotherapy may reduce the distant metastasis rates and prolong the survival of the surgically resected stage II non-small-cell lung cancer patients.
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DOI
10.1016/S0003-4975(99)00715-8
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ICD 03
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