Non-small Cell Lung Cancer Clinical Trial
Official title:
Comparison of Postoperative Adjuvant Chemotherapy With/Without Rh-endostatin: a Randomized, PhaseⅢ and Open Clinical Study of Non-small Cell Lung Cancer in PhaseⅠB
- Lung cancer is one of causes of the malignant tumor-associated death on a global scale,
in which the surgery is the only effective approach in patients with non-small cell
lung cancer (NSCLC). As present, the total postoperative 5-year survival rate of NSCLC
is 40%, while only 4%~15% patients can benefit from adjuvant chemotherapy[1]. American
National Comprehensive Cancer Network (NCCN) manual recommends that adjuvant
chemotherapy can be performed on NSCLC patients in phase Ⅱ~ⅢA.
- In order to assure the necessity of adjuvant chemotherapy on NSCLC patients in phase ⅠB
or which kind of patients would benefit from it after the establishment of new staging,
a multi-subject group of lung cancer set up a perspective, randomized, open clinical
trial to explore whether adjuvant chemotherapy was effective on NSCLC patients in phase
ⅠB under new staging policy, and to collect the characteristics of patients who could
benefit from the treatment and the better adjuvant drugs after operation.
- In postoperative adjuvant chemotherapy, navelbine plus platinum (NP), the most commonly
used therapeutic protocol, had more advantages than other 3 generations of new drugs
plus platinum. With the continuous implementation of individual therapies for lung
cancer, some new drugs became selective to pathological patterns and gene types, and it
was unclear whether these drugs would be more effective than conventional drugs in
postoperative adjuvant chemotherapy. The first- and second-generation of drugs were not
observed with survival advantages except the third generation, so what conclusion would
be made in selecting individual chemotherapeutic drugs according to pathological
patterns? In this study, Pemetrexed plus Platinum were adopted in postoperative
adjuvant chemotherapy on patients with adeno-carcinoma, while Docetaxel plus Platinum
were performed on those with non-adeno-carcinoma.
- Apart from individual chemotherapy on the basis of different pathological patterns,
anti-angiogenesis therapy has been quickly developed in recent years, becoming the most
effective approach to improve chemotherapeutic efficacy. The main mechanism of
anti-angiogenesis drugs includes inhabiting tumor angiogenesis to postpone or inhabit
the recurrence of residual tumor through reconstructing the balance of
anti-angiogenesis and preventing the growth of micro-metastasis to keep it in resting
stage. The effect of adjuvant chemotherapy can be promoted by increasing the drug
sensitivity, and survival time can be prolonged though further delaying the time and
decreasing the rate of postoperative recurrence and metastasis of tumor by
anti-angiogenesis therapy combined with adjuvant chemotherapy. As more attentions are
increasingly given to anti-angiogenesis drugs in postoperative adjuvant chemotherapy at
present, Endostar, an anti-angiogenesis drug studied independently in China, had
favorable effect in treating advanced lung cancer when combined with chemotherapy.
Therefore, this study protocol to gather the effect of Endostar on improving the
survival of early lung cancer patients by observing its effect on partial NSCLC
patients in treatment group when combined with other therapies.
- A total of 392 NSCLC patients in phase ⅠB were selected in this perspective,
randomized, open and control clinical trial, in which 262 and 130 patients served as
research and control groups respectively by 2:1. Patients 4-8 weeks after operation
were divided according to different high risk factors. A total of 4-week different
chemotherapies (21 d as a course) were given to patients with different pathological
patterns in research group, in which adeno-carcinoma group and non-adeno-carcinoma
group were treated by Pemetrexed plus Cis-platinum and Docetaxel plus Cis-platinum,
respectively. Then, above two groups were randomly divided into two subgroups
respectively by 1:1, with subgroup 1 being treated with original chemotherapies while
subgroup 2 being added with rh-Endostatin therapy.
- High risk factors included poor differentiation (including neuro-endocrine carcinoma),
blood vessel invasion, wedge incision, tumor diameter >4 cm, visceral pleura
involvement, ambiguous N staging and incisal edge <1 cm.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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