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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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1350493 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% u1 s7 Z* x% {
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
  @3 B- G0 h8 d/ y+ Author Affiliations
; T1 l2 p* l  J+ @( B2 r7 C- ]
$ G3 h' E7 |8 g: R) y. I( B1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
$ M. g# g) w8 k6 E( v  q2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 e  e! g! C& F. S' W" q3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 y( l) L2 F" B
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 4 X  x% a' q: M5 g- o3 d: v& O
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
: }! k* U* Q0 q" D9 p, f0 a" |6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
5 ^9 k+ t0 |* L) }) ]! k2 i7Kinki University School of Medicine, Osaka 589-8511, Japan
! \; K& u+ W& T( Q" m8Izumi Municipal Hospital, Osaka 594-0071, Japan
3 w/ N) ?  {, z9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan # a& E/ Z0 a: X5 O
Correspondence 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
* |, M/ N+ S9 }8 ]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. 4 b- |/ U" ?1 Y' A6 N2 W- W
; U1 W( |- f+ P2 u
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
$ w& o" k( Y9 k1 {) P# \; X9 }+ s. k( c9 ]- P; E! r
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' k) D. _! s- E
- [/ m5 {1 `! M) k, _' L: z
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
! G: ^3 z: x# T" d" f# I" ~
. ^" I# V; V& U6 {) e+ {6 E  JPublished online on: Thursday, December 1, 2011
- L" P2 ~0 c! y. i3 L; f# J
5 q/ Y8 O: H: q) m% gDoi: 10.3892/ol.2011.507 0 D7 L8 T$ ^4 N/ A

6 _6 o7 A# f2 Q2 m' {Pages: 405-410
" |, V! z% \9 W& E* s; K  L# Q
Abstract:& w; C, I. B0 J
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.2 M5 U9 P" J5 Z! {1 ^

* h& [" v6 R- G; C
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! E$ l$ F" f5 o4 h; N
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
( I9 l) L/ W7 X1 a! [7 H& T% b: w+ Author Affiliations
% E; o$ Z  T, B# E8 r$ m5 I! i1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
8 v9 T( i& v& e0 a2Department of Thoracic Surgery, Kyoto University, Kyoto " s0 v7 S4 a) a3 A0 \4 O
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 7 N9 U+ k" q) `1 @
&#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
$ B5 c  T2 u2 {( u4 H" b3 q- ]Received September 3, 2010. 3 f% U  w) F7 y8 X/ u: x5 e% A
Revision received November 11, 2010. 2 A. Y1 m; s' h4 l: |$ E, C
Accepted November 17, 2010. 3 U% e. q8 b+ T. [; Z1 P5 F$ C( K2 C
Abstract
- x) |  x% `! h) l! h. RBackground: 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. 6 z  a$ w% Y7 Y9 {
Patients 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.
$ e2 m7 J) [) X% @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. * E* v' q6 b! \: {
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. # w% e2 `8 L/ W' k, ?. }" f
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。
9 I) U- F: k9 s4 K: @/ Z4 B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?! [2 ^! d$ V* l* j
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 Chemotherapy* B* J5 z5 t: Q/ J: p9 ~$ Q
http://clinicaltrials.gov/ct2/show/NCT01523587
( w: S+ i$ [% v& U8 J; X# ]  @' ?7 y' q4 }: A* q& d9 n* B' d
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' m: U% T: K8 e4 _4 Uhttp://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 ( l# |" ~( o5 n: D- i3 w

! G8 L/ M/ N; p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。, F0 l: R! p6 A
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

( E0 c7 l8 H+ E2 ^+ g, q! C没有副作用是第一追求,效果显著是第二追求。
2 w* S# d0 P# X: c# t不错。

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