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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1405790 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type( c& q  [( H! f
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 1 x8 t8 _3 F( z% r- K
+ Author Affiliations
/ K1 k; l; t0 s, T. R1 k" e5 C, e& v
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
' e) Z) x- I. ?& a. n3 j) b2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* s$ _, Y+ z4 q7 D6 _' A9 ]3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; Z+ A4 B4 S& n3 a, T! K2 {
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
' g! h5 k5 @: M/ U5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 1 u% i0 o- |, B5 |) J& I
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
: @4 |9 W  Y( L, E1 E  R7Kinki University School of Medicine, Osaka 589-8511, Japan & q2 B. w6 i, a
8Izumi Municipal Hospital, Osaka 594-0071, Japan
* \. C& n" M( e* r5 M. C9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
3 q: ~. Z& d7 j! yCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp ; r& D7 x- ]+ H. O/ U! U
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. , h" C& R  E, ^; S& |
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato - L* Y) u% y: \9 D

1 T8 ~$ H9 p5 KAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
( Z  A, ^( V6 l! ~7 ]. Q* R
7 V: Z: D" q" M* U# t) M  ]! kPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507 % S- I3 D+ e- k! V5 W

0 P( K3 C+ @3 J7 \# s- r6 ]+ nPages: 405-410
0 X% N2 ^, z' @. _3 n' [, K6 e7 S+ ~  Z' V2 D/ M" I
Abstract:+ y) N$ R* h8 w
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.7 b, k, ~2 u2 ~3 F
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population: b8 j. N4 ?# W$ D( k
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 L( q  n/ n) e3 d( @
+ Author Affiliations0 N7 ^1 @& B2 N% M) Z4 n# E1 p
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu $ a# y8 O* O6 q
2Department of Thoracic Surgery, Kyoto University, Kyoto
" z2 f# W; o! R# K, U3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
6 |6 x! v* G5 }' V4 A&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp / m9 {  z& Z& H
Received September 3, 2010. 5 s+ j+ x+ G6 D& a+ J& l
Revision received November 11, 2010.
1 A6 S" W4 c' [  N4 ^  s- cAccepted November 17, 2010.
! f# B( B0 J# L+ ?: d: }Abstract
8 d9 ?5 _. R. h9 A4 FBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
3 ]- U1 K- o) v  NPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. , W% d0 p, h* r, z7 R
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. ) x$ L" M. t0 l7 @
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( V# k6 I6 D6 [! l- l5 |% C7 X
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
& j" o# r7 j7 H& f8 {3 C9 T今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?4 e2 ?# E% x5 r! b8 I6 J* L
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy5 m& O6 ?0 z7 W( M
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC4 f( P  G& Q7 N) ^. @( m; A
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 / f9 W4 k) U' D) r- l
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
1 P$ R' {6 ^5 X2 H& _4 z至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
7 z/ x5 d$ J9 Z' j" z$ m* m从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。) V% d% R+ y) q$ s7 [* S* U
至今为止,未出 ...

7 l6 U' y; I+ c) d没有副作用是第一追求,效果显著是第二追求。% E. h5 @0 ~" o# G
不错。

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