Adjuvant radiotherapy and chemotherapy for stage II or IIIA non-small-cell lung cancer after complete resection. Provincial Lung Cancer Disease Site Group.

D M Logan, C A Lochrin, G Darling, A Eady, T E Newman, W K Evans
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Abstract

Guideline questions: 1) Does the use of postoperative, adjuvant radiotherapy or chemotherapy, alone or in combination, improve survival rates among patients with completely resected, pathologically confirmed stage II or IIIA non-small-cell lung cancer (NSCLC)? 2) Does the use of radiotherapy reduce the risk of local recurrence among patients with completely resected stage II or IIIA NSCLC?

Objective: To make recommendations about the use of postoperative adjuvant radiotherapy and chemotherapy in the treatment of patients with completely resected stage II or IIIA NSCLC.

Outcomes: Overall survival and disease-free survival are the primary outcomes of interest. A secondary outcome of interest is local disease control. PERSPECTIVES (VALUES): Evidence was collected and reviewed by 4 members of the Lung Cancer Disease Site Group (Lung Cancer DSG) of the Cancer Care Ontario Practice Guidelines Initiative. The evidence-based recommendation resulting from this review was approved by the Lung Cancer DSG, which comprises medical oncologists, radiation oncologists, pathologists, surgeons and a medical sociologist. A community representative was present at 1 meeting during which the recommendation was discussed.

Quality of evidence: One meta-analysis and 22 randomized controlled trials (RCTs) were published between 1962 and 1996. The RCTs compared surgery plus radiotherapy with surgery alone; surgery plus adjuvant chemotherapy with surgery alone; surgery plus radiotherapy with surgery plus both chemotherapy and radiotherapy. Many studies included patients with stage IIIB NSCLC; some included patients with incompletely resected stage I NSCLC or with small cell lung cancer (maximum 10%). Older studies used chemotherapy or radiation that would now be considered inferior according to current standards of practice.

Benefits: There was no survival benefit with adjuvant radiotherapy alone, although 3 RCTs reported a reduction in the rate of local recurrence among patients treated with adjuvant radiotherapy. The meta-analysis showed that postoperative, cisplatin-based chemotherapy alone reduced the relative risk of death by 13% (hazard ratio [HR] 0.87, 95% confidence interval [CI] 0.74 to 1.02); in combination with radiotherapy it resulted in a 6% reduction in the relative risk of death (HR 0.94, 95% CI 0.79 to 1.11).

Harms: Postoperative adjuvant chemotherapy with alkylating agents was found in the meta-analysis to increase the relative risk of death by 15%. A study involving prolonged adjuvant chemotherapy (busulfan or cytoxan daily for 2 years) reported that 4 of 726 patients had hematologic malignancies. In 1 study, only 53% of patients received all 4 cycles of chemotherapy with cyclophosphamide-doxorubicin-cisplatin (CAP); in another, 22% of patients refused therapy with CAP because of nausea and vomiting.

Practice guideline: There is evidence from RCTs that postoperative radiotherapy reduces rates of local recurrence by 11% to 18% (or 1.6 to 19-fold) among patients with completely resected, pathologically confirmed stage II or IIIA NSCLC. Therefore, if the outcome of interest is a reduction in the frequency of local tumour recurrence, radiotherapy is recommended. However, there is no evidence of a survival benefit from postoperative radiotherapy alone. In a meta-analysis, postoperative chemotherapy with or without radiotherapy resulted in a slightly reduced (statistically nonsignificant) risk of death among patients with surgically resected stage II or IIIA NSCLC. The survival benefit was small and achieved only with chemotherapy regimens that produced substantial toxic effects and that are no longer used. Newer chemotherapy regimens are currently being evaluated as adjuvant therapy, but there is insufficient evidence of benefit at this time to recommend them. Therefore, if the outcome of interest is survival, there is insufficient evidence to recommend current chemotherapy regimens with or without radiotherapy as postoperative, adjuvant the

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II期或IIIA期非小细胞肺癌完全切除后的辅助放疗和化疗。省肺癌疾病现场组。
指南问题:1)单独或联合使用术后辅助放疗或化疗是否能提高完全切除、病理证实的II期或IIIA期非小细胞肺癌(NSCLC)患者的生存率?2)放疗是否能降低完全切除的II期或IIIA期非小细胞肺癌患者局部复发的风险?目的:对完全切除的II期或IIIA期非小细胞肺癌患者术后辅助放疗和化疗的应用提出建议。结局:总生存期和无病生存期是主要的结局。次要结果是局部疾病控制。观点(价值观):证据由安大略癌症护理实践指南倡议的肺癌疾病现场组(肺癌DSG)的4名成员收集和审查。这项审查得出的循证建议得到了肺癌研究小组的批准,该小组由医学肿瘤学家、放射肿瘤学家、病理学家、外科医生和医学社会学家组成。一名社区代表出席了讨论该建议的一次会议。证据质量:1962年至1996年间发表了1项荟萃分析和22项随机对照试验(rct)。随机对照试验比较了手术加放疗与单独手术;手术加辅助化疗,单独手术;手术加放疗手术加化疗和放疗。许多研究纳入了IIIB期NSCLC患者;一些患者包括未完全切除的I期非小细胞肺癌或小细胞肺癌(最大10%)。以前的研究使用的是化疗或放疗,根据目前的实践标准,这些疗法现在被认为是次等的。获益:单独辅助放疗没有生存获益,尽管3个随机对照试验报告了接受辅助放疗的患者局部复发率的降低。荟萃分析显示,术后单独以顺铂为基础的化疗可使相对死亡风险降低13%(风险比[HR] 0.87, 95%可信区间[CI] 0.74 ~ 1.02);联合放疗可使相对死亡风险降低6%(相对危险度0.94,95%可信区间0.79 - 1.11)。危害:荟萃分析发现,术后使用烷基化剂辅助化疗可使相对死亡风险增加15%。一项涉及延长辅助化疗(每天布苏凡或环磷酰胺2年)的研究报道,726例患者中有4例患有血液恶性肿瘤。在1项研究中,只有53%的患者接受了所有4个周期的环磷酰胺-阿霉素-顺铂(CAP)化疗;在另一项研究中,22%的患者因恶心和呕吐而拒绝接受CAP治疗。实践指南:随机对照试验的证据表明,在完全切除、病理证实的II期或IIIA期NSCLC患者中,术后放疗可使局部复发率降低11%至18%(或1.6至19倍)。因此,如果治疗的目的是减少局部肿瘤复发的频率,则建议采用放疗。然而,没有证据表明单纯术后放疗能提高生存率。在一项荟萃分析中,手术切除的II期或IIIA期非小细胞肺癌患者术后化疗加放疗或不加放疗导致死亡风险略有降低(统计学上无统计学意义)。生存获益很小,只有在化疗方案产生大量毒性作用并不再使用时才能实现。目前正在评估新的化疗方案作为辅助治疗,但目前没有足够的证据表明它们有益。因此,如果关注的结果是生存,没有足够的证据推荐目前的化疗方案加或不加放疗作为术后辅助治疗
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